Science topic

Thyroid - Science topic

Research in basic and clinical thyroidology.
Questions related to Thyroid
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I am working on a project involving tissue-resident memory T cells in the thyroid, and CD69 is a key marker for these cells. However, I’ve struggled to find a CD69 antibody that works effectively for immunohistochemistry on paraffin-embedded (IHC-P) mouse thyroid tissue. I am particularly interested in antibodies that have been validated in similar studies. If anyone has experience with a specific CD69 antibody for this application, your insights would be extremely helpful.
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Please take a look at clone H1.2F3.
PE anti-mouse CD69 Antibody
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My major research area is clinical research and basic research of thyroid and parathyroid.
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Video-Assisted Thoracic Surgery, Video-Thoracic Surgical Treatment of TB-Empyema
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After Performing histology for 3 attempts I am not getting the good sections. I need hints and tips for the thyroid histology from zebrafish head.
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Zebrafish is a powerful model organism, particularly for understanding vertebrate development owing to its optical transparency in the early stages of development and the availability of new technologies for dissecting gene function. The study of the thyroid consists of a chain of events beginning with the morphogenesis of the gland and followed by maturation of the follicles, acquisition of functionality, and formation of the vascular network. These processes should be carefully characterized and documented in such a way that they can be accurately reproduced and standardized for cross-comparison of results coming from different experiments, mutant genotypes, and treatment conditions. Recent advances in imaging technologies permit detailed and sequential observation of even small-sized models like the zebrafish (Marelli et al., 2021).
Marelli, F., Rurale, G., & Persani, L. (2021). From Endoderm to Progenitors: An Update on the Early Steps of Thyroid Morphogenesis in the Zebrafish
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Dear RG group,
We are going to examine different AI models on large datasets of ultrasound focal lesions with definitive (patological examination after surgery in malignant leasions and biopsy and follow up in benign ones) final diagnosis. I am looking for images obtained with different us scanners with application of different image optimisation techniques as eg harmonic imaging, compound ultrasound etc. with or without segmentation.
Thank you in advance for your suggestions,
RZS
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Thyroid nodules are a common occurrence in the general population, and these incidental thyroid nodules are often referred for ultrasound (US) evaluation. US provides a safe and fast method of examination. It is sensitive for the detection of thyroid nodules, and suspicious features can be used to guide further investigation/management decisions. However, given the financial burden on the health service and unnecessary anxiety for patients, it is unrealistic to biopsy every thyroid nodule to confirm diagnosis.
Regards,
Shafagat
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I 131 therapy of the thyroid is mostly followed by a planar or SPECT scan with a gamma camera and High Energy collimator.
The thought is that a better quality scan with I 123 would be feasible and could be used for Dosimetry thus omitting the need for a I 131 scan after therapy.
Can this be done and/or is there any experience with this already? Please your input
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Also, if you're planning on administerng the 123I a few days before the actual therapy with 131I, it usually is the case that the uptake of iodine the first time, for dosimetry, might not be representative of the uptake a few days later, for treatment. Many factors, such as supression of medication to increase iodine uptake, diet changes and so forth contribute to that effect.
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I would like to measure the area and diameter of thyroid follicles on a photomicrograph using image J (see attached image). Does anybody have a simple method for doing this given the large number of follicles in a single image?
What I am specifically hoping is possible.
1) Get an area/diameter for the entire follicle including the epithelium lining (in the high mag image this is the dotted black line)
2) Get an area/diameter of the colloid (blue dashed line and star region)
I would like to do this for the low magnification image attached that shows the large number of follicles separated by "interstitium" which is connective tissue and blood vessels.
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It can absolutely be done with ImageJ or FIJI or other softwares. Lots of people do it by drawing each cell which is very time consuming and needs to be done accurately. FIJI and ImageJ have plug-ins available online and one might be a good fit for you to semi-automate this process. I personally use a plugin that detects CSA automatically based on membrane staining in muscle. Check out their library to see if one could help you save time and increase reproducibility.
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Hi everyone,
I'm currently working on a protocol to stain thyroid receptors in zebrafish but I'm having some difficulties with my signal. The protocol I started with included 2% TritonX-100 during primary antibody incubation. I was suggested to exclude Triton or any other detergent while incubating with primary antibodies but I've also read a few protocols that use detergent together with the primary antibody instead of only applying it for permeabilization. What is your opinion on that? Should detergents overall be left out of the primary antibody incubation step or does it depend on the antibody?
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When staining for thyroid receptors in zebrafish, the use of detergents during the primary antibody incubation step can have both positive and negative effects on signal intensity and specificity. Triton X-100 is commonly used as a detergent to permeabilize cell membranes and allow antibodies to access intracellular targets. However, the inclusion of detergents during primary antibody incubation can also lead to non-specific binding or reduced antibody-antigen interaction, leading to weaker or inaccurate staining results.
In general, it is recommended to avoid the use of detergents during primary antibody incubation unless there is a specific reason to include them, such as if the antigen is intracellular and difficult to access without permeabilization. However, the specific antibody being used and the tissue or cell type being stained may also affect whether or not detergents should be included during primary antibody incubation. For example, some antibodies may require the presence of a detergent to effectively bind to their target antigen, while others may be sensitive to the presence of detergents and require exclusion during the primary antibody incubation step.
It is also worth noting that the concentration of detergent used can also affect staining results. Higher concentrations of detergent may lead to increased permeabilization and better access to intracellular targets, but may also increase non-specific binding and reduce signal specificity.
In summary, the use of detergents during primary antibody incubation in thyroid receptor staining in zebrafish should be approached with caution and optimized for each specific antibody and experimental condition. It may be necessary to test different protocols to determine the optimal conditions for your experiment. Consulting the literature or antibody manufacturer's recommendations can also be helpful in determining the best approach for your specific staining protocol.
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We will be conducting research on the potential effects of various exercise modalities on thyroid function in primary hypothyroidism.
The available research is paper-thin, mostly old studies relating to subjective measures of physical activity and largely focused on obese women to the exclusion of (the many) women having a normal body habitus and still suffering from hypothyroidism.
If you know of any ongoing trials, or past publications centred specifically on exercise intervention (not physical activity) in PHT, with proper monitoring of thyroid function, kindly leave links or revert to me by PM or comments below.
Thank you.
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I hope you don't mind this comment: I would like to suggest (if, of course, you have not already included it) that you include assessment of serum T3, serum reverse T3 and serum T3/rT3 ratio, as a parameter, in your calculations: you may find a consideration of the T3/rT3 helpful.
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Thyroid function tests are conducted in order to determine the cause of abnormal thyroid function. These are also used to tell if your thyroid gland is functioning properly by measuring the amount of thyroid hormones in your blood. What are the different thyroid function tests to be used in order to tell if the thyroid is healthy or not?
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The thyroid set of thyroid function tests includes the TSH measurement by third-generation radioimmunometric assay, as well as the total and free thyroid hormones quantification. Free T4 (FT4)measurement is more valuable for diagnosing impaired thyroid function than total T4 because the free T4 fraction is not modified by factors that alter the thyroid hormone-binding proteins. Some laboratories also include free thriyodothyronine (FT3) as part of the thyroid function set. The usefulness of the set of thyroid function tests is to confirm whether the function of the thyroid gland and its relationship with the pituitary gland is normal or not, to investigate anomalies in the proteins transporting thyroid hormones, cases of tissue resistance to the thyroid hormones as well as tumors producing TSH. In the latter two cases, the TRH stimulation test is useful.
A thyroid function study can be done as a screening research study consisting of the quantification of TSH in the general population as a research tool to determine the prevalence of thyroid dysfunction or in case of the presence of risk factors of thyroid dysfunction, such as first degree relative with altered thyroid function, pregnancy, type 1 diabetes mellitus and subjects over 60 years of age, among others. In these cases, it is only necessary to measure serum TSH hormone, since it is the most sensitive test to assess alteration of thyroid function, and perform free T4 and TSH measurement if the clinical data are very suggestive of thyroid dysfunction, which avoids duplication of studies, and medical consultations. The treatment in case of suspected low thyroid function with normal thyroid profile tests is not justified since the symptoms are non-specific.
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My lab is working in a project where we collect residual material from thyroid FNA biopsies.
We collect the residual material by "washing" the syringe in RNA later solution (in the eppendorf) right after the FNA biopsy is done.
Since it's not a lot of sample to start with, considering that the material is diluted in ~200 uL of RNA later, how could we improve the concentration yield for DNA and RNA?
We've used Invitrogen PureLink and Qiagen QiAMP extraction kits for DNA isolation, but our concentrations are around 1-2 µg/ml most of the time and OD varies a lot.
As of RNA extraction, we've tried TRIzol + Chloroform protocol, but same concentration problem happened.
Has anyone worked with thyroid FNA biopsies sample before? Is this a normal concentration? Any tips on improving them?
Thanks!
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How did you do sample disruption and homogenization before RNA extraction?
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Hi,
is there any method to detect iodine uptake by thyroid cells in vitro different from radio active iodine?
Thankyou
Francesca
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RAIS gamma camera
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Hi all, Anyone knows how to get the images data set of SPECT Iodine-131? for patient thyroid ablation..
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I agree
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Induction of hyper and hypothyroidism in rats by drugs (LT4 and carbimazole), is the protocol scientifically valid to study the effect of bioactive compounds against thyroid dysfunction?
(pharmacological and clinical study)
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The guideline outlines testing for thyroid dysfunction in patients , including pregnant women or women planning pregnancy, and the monitoring of patients treated for primary thyroid function disorders. It does not apply to the BC Newborn Screening Program. This guideline outlines testing for thyroid stimulating hormone (TSH), free thyroxine (fT4), free triiodothyronine (fT3) and anti-thyroid peroxidase (TPO).
Information on other tests, including thyroglobulin/antithyroglobulin (Tg/anti Tg) and antibodies to the thyroid stimulating hormone receptor (TRAb), are covered in the associated BC Guideline
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I want to see prevalence of PE and ED in patients with thyroid derangement. I found in one study, in case of hyperthyroidism, prevalence of PE and ED is 50% and 14.7% respectively and in case of Hypothyroidism, prevalence of PE and ED (along with HSD and DE) is 7.1% and 64.3% respectively. They worked with only 48 patients. their study design was prospective study as they followed up the same patients once.
my study is cross sectional. As it is for thesis purpose , a small sample will be convenient for me. Please suggest me.
Thanks in advance...
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To estimate a prevalence (P), the sample size is: n = z²PQ/u². With Q= 1-P, u = required precision, z = 1.96 for α = 5% . If several estimates of P are advanced, the one that generates the largest sample size is selected. At the same required precision and α error , the estimated sample size is the greater the closer P is to 50%. If we have no idea of P, we can adopt the most unfavourable situation where P = Q = 0.50. Hence: n = z²/4u². For example, for an required precision of 0.020 (2.0%), at risk 5%, the sample size to be taken is: n = 1.96² / (4 * 0.02²) = 2401.
To avoid all these calculations use the free OpenEpi calculator :
Sample Size for % Frequency in a Population (Random Sample)
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Hi all! I am hoping that this is a simple ID for someone who knows what they're doing.
I am looking at transverse sections of the base of the heart. In several there are small groups of large, round cells. They appear to be highly organized and always appear near the left atria, which makes me believe they are part of an established organ. I was leaning towards parathyroid, but the reference images don't quite convince me. Then I found a piece that appears to be within the mitral (?) valve of one sample, so I'm at a loss again.
I have attached images from two different samples: one where there are 3 distinct pieces all within fat and one with the valvular location. Initially I thought that was an embolus of some sort in the valve, but I'm thinking now it may just be atria that got smushed down during embedding.
I promise I"m taking all of my images to a histologist for final say, but I would like to have some idea of what's going on before then. Any input would be very much appreciated!
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These are the ganglionated plexuses of the heart which lie within the epicardial fat predominantly in the atria. You can also see the beginning of a nerve in "high zoom top.png". The individual cells are called ganglion cells. You can confirm using immunohistochemistry such as PGP9.5 or NSE.
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Hello everyone,
As you've probably guessed I'm fairly new to Geant4 and I am working on a project where I have to determine energy deposits in various organs after Irradiating the thyroid with I(131).
For starter I want to use the available human phantom just to get the gist of it but my problem is how should I simulate the radiation, provided that Iodine is concentrated in the thyroid and that it has a half life of 8 days, said Iodine disintegrate by emitting an electron and a gamma ray.
My questions are many:
1/Should I take the thyroid as the point from where the radiation is being emitted?
2/How will the half life be taken into account?
3/Do the organs provided in the example have sensitive detectors or should I create them?
4/How does the scoring goes?
All in all I would appreciate any and all help and if anyone has a clear idea of how I should proceed please your help is most welcome.
Thank you.
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Hello,
Thank you Hadi Jabbar Alagealy & Keyvan Tabaei for responding to my question.
I will try to explain myself better so you would get a clear idea of what I am trying to achieve.
I have sent you a message and I would be very glad if you responded.
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From a medical and scientific point of view, without any other dimensions or object from my question?
thyroid autoantibodies prevalence in iodine deficient are 13%
sufficient are 18%
excessive are 25 %
iodine prophylaxis in previously iodine deficient areas up to four-fold increase in prevalence of thyroid autoantibodies was demonstrated after the exposure to higher iodine intake
my question what are the opinion about the prophylaxis program?
give me the opposite view, positive side as possible as
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You are welcome! I will try to find the proper articlre and send you .
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Since its first use several decades ago, scanning electron microscopy has been used in
numerous investigations dedicated to biological systems. This contribution focuses on observations on pathological calcifications in order to review several major applications of primary importance to the clinician. Among these, we highlight such observations as medical diagnostic tools in pathologies arising from primary hyperoxaluria and urinary infections.
More information on
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Why not. Do you think you can copy my comments in your forum. I am in holliday now.
Thanks in advances.
take care
D. Bazin
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Dear colleagues,
I'm looking for a data set (not: reference values) of at least serum and possibly urine electrolytes for some modelling in order to test a hypothesis. Having more data available (esp. related to Parathyroid, D-Vitamines and Thyroid) would be nice, as well as having information about any disease or if healthy subject .
Thank you!
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Which theory is most plausible in your opinion regarding the cause of thyroiditis after immunotherapy?
the NK and monocyte increasing after use of anti PD-1 Ab
or the blockade of peripheral tolerance inside the thyroid because the thyroid tissue highly expresses the PD-L1.
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Immune Checkpoint Inhibitors (ICIs) enhance anti-tumour responses. ICIs may prompt the immune system to attack healthy organs causing adverse changes in the skin, GI tract and endocrine system. Thyroid dysfunction is a common endocrine side effect. The administration of ICIs may trigger T
cell-mediated pathways that induce subsequent thyroid dysfunction. PD-1 or PDL-1 blockage is likely to trigger pre-existing CD8+ T cell activation. For thyroiditis, the effect of anti-PD-1 and anti-PDL-1 agents could be more than anti-CTLA-4 agents.
Treg plays a role in the inhibitory effect through cell-cell contact and secreting a regulatory cytokine IL-10. The decrease of IL-10 may be related to increase in TPO antibody suggesting loss of Treg energy and development of thyroid irAEs. Studies have shown that CD4+ Th1 which express IFN gamma and IL-2 is increased and there is a decrease in G-CSF after anti-PD-1 treatment. G-CSF has a strong positive correlation with Th2 cytokine and could cause a decrease in Th2 cytokine activation indicating increased Th1 dominance in thyroid irAEs.
Whether NK cells and monocytes are involved in thyroid irAEs needs further investigation.
Best,
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I'm conducting a retrospective study on diagnostic accuracy in detecting thyroid malignancy for 2 different ultrasound scoring systems. The same cohort will be scored based on both scoring systems and their pathological report reviewed to determine the malignancy pick up rates. When do I do the calculation for power of study - Is it before or after? And what test should I be using?
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This seems like the comparative evaluation of two different ultrasound diagnostic methods against a gold standard of pathologic malignancy.. You should just compare the sensitivity, specificity, positive /negative predictive power of the two tests, bearing in mind that these are dependent on prevalence of the condition.
Power calculations are not necessary.
Alternatively,if you are interested in incidence of path malignancy in those scored positive by ultrasound 1 vs ultrasound 2. This is a comparison of two rates. For a given sample size you can calculate the power of detecting a given rate difference
or ratio at a given alpha significance level . Alternatively you can choose a sample size for required power. These calculations should be done before the study.
referenced stats program suite covers all of this.
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Hello everybody!
We are a group interested in the study of Endocrine Disruptors, particularly focused of PFAS effects on thyroid cells in vitro. We were wondering if there is anyone else interested in this field who is available for idea exchange, and eventually collaboration.
Furthermore we are looking for a group of young researchers involved in the study of endocrine disruptors. Do you know if a group like this already exist, maybe among some Scientific Society?
Thank you,
Francesca Coperchini and Laura Croce
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Hello Liliana,
we are very experinsed in testing of PFAS for all kinds EDC mode of actions and espcially for the thyroid hormone axis with our anti-TR, TPO and TTR-TR CALUX. If you are further interested to cooperate with us, please let us zoom/TEAM soon. Greetings Peter (peter@bds.nl)
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Every article I have read, Hashimoto’s thyroiditis (HT) is characterized by (1) lymphatic infiltration, (2) formation of intrathyroidal secondary lymphatic follicles which present with a mantle zone and well-formed germinal centers, (3) obvious signs of activity within the GC (eg, lymphoblasts in mitosis), and (4) Hurthle cell changes. In the studies I've read, 100% of patients whose thyroids were excise showed these changes.
Thus, it appears to me, that an absence of germinal centers would be inconsistent with reactive changes as a result of HT (because there is no reaction occurring). If not consistent with HT, what would nodular growth with calcifications, lymphatic infiltration with absence of GC be consistent with?
I would very much appreciate comments and suggested articles.
Thanks.
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Also, atrophic thyroiditis is considered another variant of autoimmune thyroiditis. (The fourth one).
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How would expression of a gene targeted by thyroid hormone be affected by deletion of thyroid hormone receptor in the absence of hormone? How about in thyroid hormone-treated cells? Please, elaborate your answers.
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Dear Dr. Mikhail Shepetko,
Thank you for kind feedback. It's certainly useful to me. Again, you have shared your personal experience, that's impressive. Warm regards.
Sabuj Das
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20 yr old Male elevated T4, normal TSH. April 2020 TSH plummeted to .025. RAI administered April 2020. T4 remain elevated throughout. Return of hyperthyroid symptoms and 49% uptake scan 11/2020. R/O GD...
Second RAI? Thyroidectomy?
Possible pituitary thyroid resistance hormone
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Before making a special test, it may be good to see the TSH levels are elevated after the administration of high levothyroxine doses, indicated because of the diagnosis of thyroid carcinoma. (To see if they are still inappropriately high). If not practiced before, and the TSH levels continue to be high a pituitary magnetic resonance would be useful. Also, the pathological study of thyroid tissue does not explain the cause of thyrotoxicosis.
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When a patient has more than 5 TSH (Thyroid-Stimulating Hormone) but T3 (Triiodothyronine) and T4 (Thyroxine) are normal , that means the patient has Hypothyroidism. The common symptoms of Hypothyroidism are over weight, depression, hair loss, dry skin etc. Nutritional deficiencies are the sole cause of an underactive thyroid problem. Making the dietary changes can be the first step for natural hypothyroid treatment. Increasing the intake of food with vitamin A, B, D, iron, zinc, selenium, Omega-3 fally acids and iodine can help to reactive thyroid. Decrease the intake of refined foods, sugar, saturated fats, white flour , certain vegetables : broccoli, cauliflower, cabbage etc.
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Enough dosage of once daily L-Thyroxine to bring down TSH to normal range.
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I would like to differentiate this from glaucomatous visual field loss
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Freitag SK, Tanking T. A Nomenclature to Describe the Sequence of Visual Field Defects in Progressive Thyroid Eye Disease-Compressive Optic Neuropathy (An American Ophthalmological Society Thesis). Am J Ophthalmol. 2020;213:293-305. doi:10.1016/j.ajo.2019.12.005
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I am asking this question on behalf of my colleague who has to do thyroid's elasticity scan of normal population. This data will act as reference value in order to compare with diseased one. So, how can one determine if 100 samples would be adequate sample size or not? Regards
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Anoop Krishna Gupta if/when you don't know the sample size and the study population comprises of general public , the sample size is 384.
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I am looking for plasmid and vector for human receptor on yeast. I am working on thyroidic and androgenic receptors. I would like to have your feed-back about what it is possible to use and who is the best provider for such vectors?
Thanks in advance.
Thomas
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Thanks a lot for these advices
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Girls
Overweight
sleep a lot
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I am looking to treat thyroid tissue with Iodine-131 and need to hold the tissue in a 'contaminated tissue' freezer, although the freezer is -20C as opposed to -80C. I usually store all tissue at -80C, but in this case it's not possible. Will the difference in temperature have a deleterious effect on the tissue?
Thanks in advance
Andy
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thank you for your answers everybody. Much appreciated
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Does garlic have an effect on this hormone and decrease or increase them?
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Please take a look at the following PDF attachment.
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The woman was found sever hypothyrodism at 13 weeks of gestational age. Her TSH was 110 mU/L, FT4 4 nmol/L, and TPOAb-, TGAb-. She was performed partial thyroidectomy for thyroid cyst at 7 year-old. This pregnancy should be continued or terminated?
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Pregnant Woman with sever hypothyroidism may be on risk of abortion, and if she don't the neonate may have a hypothyroidism and neonate should receive treatment to avoid neurological disorder caused by hypothyroidism.
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There is a bidirectional flow of fetal and maternal cells in pregnancy. Fetal cells migrate and resides in breast tissue, thyroid tissue, skin and so on in mothers body. How can we detect these fetal cells in mothers tissue?
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This is called microchimerism, sometimes -if sustained until few months postpartum- detectable by the immune system leading to autoimmune disease.
Detection methods include -beside Y chromosome as said above- HLA typing.
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I am working on the history of diagnosis and treatment of thyroid gland and diseases in orient and occident. Who can help me to find more historical references from Egypt, China, Greece, Persia, India...
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The thyroid is a small tissue part of the neck that surrounds the throat and trachea and is attached to a couple of thyroid glands that regulate calcium in the blood. It controls the metabolism of all cells in the body. When the thyroid gland has many health problems, such as lack or increase of hormones, it adversely affects the rest of the body. So, there have been many studies and recent scientific research that proved that the practice of yoga exercises regularly contribute greatly to the treatment of thyroid problems.
 
There is a new American study entitled (Yoga and its impact on thyroid activity) published by the site of Life proves that the practice of hot yoga regulates thyroid secretions. As many yoga movements and positions within hot yoga halls help greatly enhance thyroid functions.
 
Hot Yoga is one of the most famous body and soul sports established by Bikram Choudhary and developed hot yoga at temperatures ranging from 95 to 105 Fahrenheit and 40% humidity. These studies have shown the benefits of yoga to increase the secretion of thyroid hormones in the case of inactivity. The practice of yoga regularly able to flow blood to the neck area, which helps in the secretion of thyroid hormone.
 
June 21, 2014 The United Nations announced that this day is the day of universal yoga practice. Where it is one of the largest events in the world, especially in the State of India. Because yoga has been established for 5,000 years in India and is one of the most important Indian customs, traditions and cultures. It is also a distinctive sport that includes mind, body and spirit. It also helps to feel comfortable and relax and solve many health problems especially thyroid problems.
 
Medical studies in the field of natural remedies have confirmed that all patients with thyroid problems and lack of activity must exercise in yoga. The position of the camel and the status of cobra is one of the most important conditions in the sport of yoga to treat thyroid problems and regulate the hormones produced by this important gland. It tightens the muscles of the neck, shoulders and neck and prevents hyperthyroidism or infection.
 
As another study by Tanta University in Egypt has shown, "Thyroid hormone controls the weight," says Dr. Essam Alwan, consultant gastroenterologist and endocrinologist: "The thyroid gland is considered to be the master's glands. Therefore, the practice of yoga limits the high blood cholesterol level, which causes an increase in weight and obesity, and thus affect the hormones responsible for the thyroid gland and suffer many problems.
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We use purified hTSH (in PBS), but have issue with stability of the sample. Since the purified hormone is highly unstable the activity reduces drastically at room temperature. We had added BSA to the buffer but it causes hindrance in our immunoassay protocol.
We would like to know what other ways (buffers, additives) can be used to stabilize the hormone for use at room temperature?
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Rohan Aggarwal Proclin 300 is antimicrobial and prevents the growth. Since thyroid hormones are proteins they will require stabilizers to keep them stable. Also add a zwitterionic detergent like CHAPS.
I agree with Antonina Kokisheva that there is no information available in regards to the composition of commercially buffers. But buffers from CANDOR and Surmodics does give good stability.
You can try PBS buffer with Methionine(100-300mM), Lysine(100-300mM), NaCl(50-200mM), EDTA(1-10mM), 1 to 2 % glycerol, Proclin- (0.01-0.1%) (*I also use BSA in this composition but you can try using it without BSA)
Do share the results in terms of stability.
All the best.
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I am trying to use faster RCNN (in MATLAB) for nodule bounding box detection in a small thyroid Ultrasound dataset (only 233 images). Some nodules are big and some are very small. My question is that how can I improve the performance of faster RCNN in this challenging problem.
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Interesting discussion...Following
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Would be grateful of someone could help me find an article that sheds light on the above mentioned subject.
Thanks
Vatsal
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Depending the grade of Insulin resistante state in patient (Gut, Adipose, Liver, Muscular) and the optimal function of the Brain-Gut-Axis, the ethinilestradiol, the testosterone, the Dehydrotestosterone and The Progesterone in women, all of this (metilpregnenolone, ever...) hormones dinamic equilibrium, sum the acute cortisol and adrenaline activity, modulates the amygdalar reactivity and the memory process. In acute way, the central brain Insulin determinates the memory consolidation, with the Melatonin control (In acute form, the Insulin Melatonin Axis),
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I've been trying and failing to obtain cell-culture grade crude TSH (probably bovine) for propagation of laboratory thyroid cell lines (ie. FRTL5) - Merck / Sigma had a suitable product in their catalogue that they deleted after I placed the order, and other companies with TSH listed are also responding that it has ceased production.
Other sources are hideously expensive - literally tens of thousands of dollars for an amount needed for 1L of culture medium because they are therapeutic grade. This is not what I need - the experiments would not be financially viable.
Does anyone know a commercial supplier with a viable and cost-effective source of Thyrotropin / bTSH?
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Dear Robin Dickinson:
I am sorry, but no, I do not have the answerto your problem.
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I am a third year graduate student in a lab that focuses on growth hormone. My project, however, is extremely thyroid hormone specific. From most of the literature I have found, it seems thyroid hormones are measured by RIA instead of ELISA. This leads me to two questions:
Is there a specific reason RIA is used over ELISA?
Can an ELISA be used to measure serum T4 and T3 levels in mice effectively?
Thanks!
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ELISA is the best and safe technique for T3 and T4 determination.
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Since the thyroid gland plays a central role in the regulation of metabolism, abnormal thyroid function can have a major impact on the control of diabetes. In addition, untreated thyroid disorder can increase the risk of certain diabetic complications and can aggravate many diabetes symptoms. Luckily, abnormal thyroid function can easily be diagnosed by simple blood tests, and effective treatment is available. For all of these reasons, periodic screening for thyroid disorder should be considered in all people with diabetes.
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There is a association between thyroid disorders and diabetes because various genetic and physiological mechanisms that lead to hyperthyroidism and hypothyroidism can also cause insulin resistance. This in turn prevents glucose from being utilized by the body, leading to diabetes. Please take a look at the following references.
Thanks!
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I wonder if there're some Elisa kits which have been identified to test mice T3/T4/TSH, I've searched R&D, and there're only T4 Kit.Or could I use the RIA machine used in clinical testing which is for human? I just worry about the blood volume could not reach RIA machine's lowest baseline.
Thank you a lot for sharing your exp.!
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Hi Frankie Yu ! For adult and postnal rats we use routinely use RIAs to quantify serum total T4 and T3 using coated tube kits from IVD Technologies (below - veterinary). We have in-house validated the total T4 kit with mass spectrometry (LC-MS) and have found comparable results across the two methods. The sample volume is not too bad either (25 ul/rxn, 50 ul total for technical duplicates). Of course for total T3 and free T4 the serum concentrations can be low depending on the animal’s age and treatment, but we have found they are generally pretty reliable.
If we are concerned that some samples are below the lowest standard, we have made a few modifications that seem to work well in our hands for the total T4 kit. First, we diluted the lowest kit standard to make one more point for the standard curve, and then we also have doubled sample volume. We then adjust the quantified T4 given this doubled volume to determine the final concentration. We have found that when doing this the standard curve is still linear and doubling the rxn volume does not seem to affect the assay. However, this does not hold true with free T4 kit and we haven’t tried this with total T3 kit. But it is worth tryimg out if you think your samples may be difficult to quantify!
TSH is tricky and requires quite a bit of volume, and our colleagues prefer to quantify using a homemade RIA. Below is a paper that describes the method. Also, don’t forget to sample all animals early in the day (we do it before noon) because of the hormones’ diurnal cycle. I hope this helps and good luck! Please let me know if you have any questions.
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Ive been researching this topic since a while and I would love to expand my knowledge in this area, Ive come across some studies claiming that selenium is effective in treating thyroid dysfunctions, and of course iodine, but I would love to know more.
Thank you in advance!
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Dear RG members
thyroid dysfunction is heterogeneous and with mutifactorial etiology, you talk about nutritional deficiency in oligoelements but we have the autoimmune factor, which is the main one (hypothyroidism and hyperthyroidism = baseball disease and hashimoto). In case of thyroiditis of autoimmune the contribution of elements or oligoelements is not significant because of the genetic factor (DR3) many patients control the hormonal balance (TSH, T3 or T4)and they underestimated the autoimmune factor.
nevertheless taking Omega-3 Fish Oil. will positively activate the immune response and inhibit the effect of autoantibodies
BEST REGARDS
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Obesity being a major problem for our Diabetes patients, GLP1A therapy has become a boon for them but on routine examination if a Thyroid scan shows either a single nodule or multiple nodules, is it safe to start GLP1A for them?
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This is wander full q .... no it is not safe
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It seems that people got them as gifts from collaborators, but not in a comercial distributor...all info is welcome :)
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Thanks anyway, but finally I got them from a colleague.
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Hi all,
Thank you for taking the time to read (and hopefully answer) my question.
I was wondering if anyone could recommend or know of a thyroid receptor beta antagonist. I have found an antagonist for the alpha thyroid receptor and an unspecific antagonist but I cannot seem to find one specific to beta.
Many thanks!
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is this in humans?
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thank you I have not read everything yet but that said This is what I am looking for Memory loss , low grade headaches , ringing in ears , thyroid issue suddenly sleeplessness after 2 exposures of Lband 1310 after 9 mins . ( radar )I had a neurologist tell me it was not possible for RF to cause headaches what ever research you can provide would be greatly appreciated . I will try to go threw all references and see if I can find something
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Hi,
Do you still have the problem, can we help?
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I'm planning to use Geant4 to calculate the effective dose for mammography examination but I faced two problems:
1. I was trying to use the human phantom in advance example but some of the organs eg liver, lung and thyroid etc are missing. People suggests I could use XCAT phantom but it is quite expensive and I'm not so sure whether this phantom is suitable for mammography dosimetry or not?
2. Unlike PET or SPECT in GATE there are no benchmark for mammography unit do I need to build it from scratch? Even I modeled the mammography unit I cannot verify my simulation results...
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The license policy shouldn't be unfriendly. We're always glad to help as far as I know.
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I am trying to follow any markers associated with thyroid abnormalities..enzyme, antibodies or any molecules
thank you
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Dear, these are some of the thyroid markers.
TSH – The most common marker used to asses thyroid function and the most sensitive. This hormone is released by the pituitary when it gets the signal from the hypothalamus. TSH levels increase when T4 levels drop, and TSH decreases when T4 levels are elevated.  Sometimes this is the only marker your doctor will order.
T4 – This is the most prevalent form of thyroid hormone made by the thyroid gland. Levels of T4 in the blood act as the feedback loop for the brain and signal it to stop producing TSH. The vast majority of it is bound to carrier proteins. It is considered metabolically inactive, and must be converted to its active form to be used by cells to regulate metabolism. Typically the only other marker tested other than TSH.
T3 – The active thyroid hormone. If it is not directly made in the thyroid gland, then conversion takes place in the liver, kidney, and GI tract. The majority of T3 is bound to carrier proteins.  Once unbound, T3 acts directly on the cell nucleus to regulate the metabolism of that cell.
Free T4 – This is the unbound version of T4. This marker can be influenced by thyroid hormone replacement, chronic illness, as well as disorders that affect the amount of carrier proteins.
Free T3 – The unbound form of T3. This is the best marker to see what amount of active thyroid hormones are available for the cells. This can be effected by stress, thyroid disorders, and pregnancy.
Reverse T3 – This version of T3 is metabolically inactive. Reverse T3 is only typically produced in cases of extreme stress such as surgery or trauma. Chronic stress can also cause the production of Reverse T3, thereby masking the adrenal issue and looking like a dysfunctional thyroid.
T3 Uptake – This measures the number of sites for T3 to bind to for carrier proteins. These are the sites that allow T3 to be transported throughout the body to be used by cells that need it. This marker is influenced by sex hormones such as testosterone and estrogen.
Thyroxine-Binding Globulin (TBG) – This is the amount of proteins in the blood that carry thyroid hormones to the cells. This marker can be influenced by infections, liver dysfunction, HRT, birth control, steroids, prednisone, aspirin, and pregnancy.
TPO Antibodies – Most commonly marker elevated with autoimmune thyroid.  90% of thyroid issues are autoimmune related.  This marker is rarely tested since there is no pharmaceutical drug to fix the problem, only lifestyle.
Anti-thyroglobulin Antibodies – Not as commonly elevated with an autoimmune thyroid condition. During thyroid cancer treatment, this marker is routinely evaluated.
Thyroid Stimulating Immunoglobulin – These antibodies are elevated with an autoimmune thyroid condition called Grave’s disease. This marker indicates a hyperthyroid state.
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Thyroxine treatment in hypothyroidism.
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A well taken answer but may not prove effective in younger individuals always .Serum TSH levels are to be estimated before as well as during dose titration.
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I am very interested in this master course in Korea. We have a clinical experience with PEIT in sclerosing toxic adenoma and metastatic neck lymph nodes (papillary thyroid carcinoma). However, with RTA we have no experience. Is there an opportunity to sign up for this couse and when it is held.
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this program is available all the year round.
please send me e mail
i will give more information
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Thyroid disorder 
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There may be a defect in the composition of the elements that feedback between TSH and T4,T3
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My group has observed that more than 70% require thyroid hormone to improve their insulin resistance indices
We hypothesize that diabetes would be a consequence of a damaged thyroid.
It would be interesting to collaborate on the topic of Diabetes and Thyroid Disease
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The cause may be indirect through the relationship of thyroid hormones and lipid Another side is lipid and insulin
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How do metals affect thyroid? And how thyroid is affected by regional variation from hilly to plain areas?
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Some minerals accumulate in the thyroid gland and that affecting on iodine, and that due hypothyroidism. in hilly and plain areas There is a difference in the nature of food, The iodine content in mountain food may be low, Coolness also requires high energy from the body to maintain temperature, this requires the action of the thyroid gland.
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We want to measure adipose tissue level of T3 and T4. According to the literatures, tissue levels of these are mainly measured by RIA. For serum samples, researchers are also using LC-MS/MS. I have three questions:
a. Can I use commercial Elisa kit for measuring adipose tissue levels of RIA? Is RIA more sensitive than Elisa?
b. Can I use LC-MS/MS analysis to determine adipose tissue T3 and T4 levels?
Your advice and recommendations will be highly appreciated.
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Hi, Afsana! The prosedure to my mind is correct. What is the retio of acetone : infranatant? Do you have any problem with the analysis? What is the recovery of the analytes?
Concerning ELISA the problen is not a sensitivity but a selectivity and as a result false positive results.
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We aim to screen for subtle motor problems in a group of children with hypothyroidism (aged 5-18 years), based on parent completed questionnaires. In Dutch the Movement ABC 2 checklist and the DCDQ '07 are the main candidates. I am familiar with the report of Schoemaker et al. (2012) "Validity and reliability of the Movement Assessment Battery for Children-2 Checklist for children with and without motor impairments.", who compared both measures. 
Which of both is internationally best known?
Which of both is most likely to detect subtle motor problems in your experience?
Thanks!
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The MABC-2-list provides norms only for the 6-12y old children. The DCD questionnaire 5-15y. 
It depends a bit on what you are looking for, because both questionnaires are mainly directed towards identification (screening) of coordination difficulties with impact on ADL activities. So, in my opinion, neither of the proposed instruments will identify 'subtle' motor problems. Moreover, in general, there is only a moderate agreement between questionnaires and more objective standardized motor assessment instruments. But then again, you will need an experienced therapist to conduct the assessments and it will be more time-consuming.
I believe the link below is an interesting article, concerning questionnaires in DCD research. 
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I am trying to compare FNA biopsy methodologies to evaluate which one gets better sample quantitatively. I would like to count total number of cells and total volume of biopsy specimen in liver/thyroid FNA biopsy. What automated device should I use?
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try using FACS - Fluorescence-activated cell sorting (FACS):  for cell counting. It can even sort your cells if you can mark the thyroid cells with a fluorescent marker
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My question is regarding this article published in thyroid in july 2016
"Effects of Levothyroxine Therapy on Pregnancy Outcomes in Women with Subclinical Hypothyroidism"
If normal free t4 is not an inclusion criteria how did they differentiate between subclinical hypothyroidism and overt hypothyroidis
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Kindly check UpToDate.com
Overview of thyroid disease in pregnancy
Author:
Douglas S Ross, MD
Section Editors:
David S Cooper, MD
Charles J Lockwood, MD, MHCM
Deputy Editor:
Jean E Mulder, MD
Contributor Disclosures
All topics are updated as new evidence becomes available and our peer review process is complete.
Literature review current through: Aug 2016. | This topic last updated: Nov 30, 2015.
Thank You.
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I'm setting up an exploratory study to look at the possible connection between iodine deficiency (ID) and several disorders. As a first step I thought I would administer a questionnaire assessing ID symptoms and compare responses to a healthy sample. But, I can't seem to find one. Likely would overlap largely with hypothyroidism, so perhaps that's a place to look. Any advice?  
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Iodine deficiency is not well correlated with hypothyroidism. In areas of iodine deficiency the prevalence of hypothyroidism is somewhat lower than in areas of iodine suficiency. 
Iodine deficiency is mostly correlated with nodular goiter. In areas of ID the prevalence of nodular goiter is higher. But goiter is symptomatic only when it is large. Small goiters are usualy asymptomatic. So you can not use a questionare for ID symptoms.
The best indicator of iodine deficiency is daily exretion of iodine in 24 h urine.
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they are many Bio-Sensors but i want only using thyroid detection.
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Mos commonly used are the carbon nanotube biosensors besides graphene bat sed elctrochemical sensors  can be used in critical situations combining these with microfluidic platforms   helps to get a bedside  realtime,and very litle volume of sample consumed,l and beta receptor detectionphabesides bacterial sensors used for thyroid aBesides luminol based chemiluminiscence can be used.
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Biochemistry, Immunology, Thyroid disorder
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Yes, also in my experience you can have high Anti-TPO levels while FT3 ,FT4 and TSH level are in range. This situation represents a risk for hypothyroidism.
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Speaking of model organisms including mice, Xenopus and zebrafish, would a total T4/T3 test be a better indicator for hypothyroidism over free T4/T3? Also, out of T4 and T3, which would be a better candidate to test for the same? Any advice would be appreciated. Thank you!
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About 95% of thyroid hormone is bound to plasma proteins - thyroid binding globulin (TBG), constituting 'total thyroid hormone'. The remainder, approximately 5%, is 'free' in the circulation and therefore metabolically active. It's worth noting that T4 is a pro-hormone, which is converted into T3 by 5'-iodinase. T3 has a higher metabolic activity than T4, but has a shorter half-life. Taking this into account, I would say free T4 (FT4) is a good assessment of thyroid hormone levels. It would also be worth testing FT3, given that there can be issues in the conversion of T4 to T3. It may also be worth testing for thyroid stimulating hormone (TSH), which if elevated, along with a depressed FT4 result, is indicative of hypothyroidism. Here's some more information: http://labtestsonline.org.uk/understanding/analytes/tsh/tab/test/. Hope that's helpful!
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Mr.Y...  is a male patient and 60 years old.he is diagnosed as type 2 diabetes and is a1c level is maintainin  7-7.4. no dyslipidemia  and  normal liver enzymes.but is thyroid level in 2 visits are are;Ft3: 3.5,   Ft4: 9.4   and  TSH :18.5.(normal range :ft3: 3.1-6.8, ft4 : 12 - 22, TSH : 1.27 - 4.2 )so dr prescribed and started levothyroxin along with diabetes medication.exactly after three months,his Ft3: 2.99, Ft4: 5.35  and TSH: 45.73 and we done anti TPO is >600IU/ml.
so can you please give some conclusion about this study?
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This is a patient with autoimmune thyroiditis and primary hypothyroidism . If TSH increases despite adequate thyroxin (2 yg/kg/daily) medication, you should consider non-compliance of the paptien or malabsorbion due to celiac disease which is often associated with Hashimoto`s disease ( Poliglandular Syndrome II/III)
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There are only a few studies on epidemiology of pediatric thyroid cancer mostly restricted to adolescents and less children (<15). Thyroid volume is smaller in children. Thus, the commonly used T-Staging in adults may underestimate the impact of tumor size on prognosis in children.
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Dear Jamshid;
Thank you so much for putting forward this interesting question. You concern about underestimation of PTMC risk is quite real in children.
1- PTC microcarcinoma is rapidly increasing in the world mainly due to availability of high resolution ultrasonography and density of endocrinologists! Children is not away from this inadvertent screenings. Ito et al from Japan showed in prospective study of >1200 patients with PTMC that surgery should not be offered to >90% of these patients. Interestingly in that report, younger patients (<40 yrs) had more chance to have progression of disease compared to  others. this is concordant with the finding that the higher the age of the patients, the higher the risk of developing thyroid nodule and PTC. So we may conclude that PMTC has more chance of progression in children than older patients.
2- Multifocality, lymphnode metastases and distant metastases is nearly two times higher in children than older patients. This finding again emphasis on more scrutiny in children in PTMC.
3-Actually TNM classification is very limited role in pediatric patients, as all patients would be categorized as stage I or II (in case of distant metastasis). Further more TNM staging is designed for prediction of death which is extremely rare in this patients. So risk stratification aimed for prediction of risk of recurrence or persistent disease is much more useful in these patients. In my own experience, first Tg( Thyroglobulin measured 6 weeks after surgery and before radio-ioidne therapy) is the most reliable predictor of recurrence or therapy failure in these patients. So I do not rely on size and I prefer to look at the neck by ultrasonography and check first Tg  and Anti-Tg Ab in off T4 state in all pediatric patients with PTC before considering it as a real PTMC,
With best regards
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Thermal image processing
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thank you sir,
data set available Uci depends on blood sample report
I required data from thermal image
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40 years old female patient with a 3,5 cm solitary nodule on left thyroid lobe.fine needle aspiration biopys confirmed atypia with undetermined significance. Which type of surgery do you prefer? Total thyroidectomy? Left lobectomy or frozen section biopsy directed surgery?
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Why to do this dr khaled where the risk of malignancy is 5 to 15 % only ?!! Frozen section isnot reliable in such cases 
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As the April 14 JAMA Oncology published that encapsulated follicular variant of papillary thyroid carcinoma (EFVPTC) is now reclassified as thyroid neoplasm with papillary-like nuclear features (NIFTP). What should we do with previously treated patient with radiodioine? Anyone can help to suggest what is the next management that should be done? 
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Dear Dr Tan
I suggest to read this paper:
Mod Pathol. 2016 Apr 22. doi: 10.1038/modpathol.2016.65. [Epub ahead of print]
Ninety-four cases of encapsulated follicular variant of papillary thyroid carcinoma: A name change to Noninvasive Follicular Thyroid Neoplasm with Papillary-like Nuclear Features would help prevent overtreatment.
Thompson LD1.
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Abstract
Encapsulated follicular variant of papillary thyroid carcinoma is a common thyroid gland cancer, with a highly indolent behavior. Recently, reclassification as a non-malignant neoplasm has been proposed. There is no comprehensive, community hospital based longitudinal evaluation of encapsulated follicular variant of papillary thyroid carcinoma. Ninety-four cases of encapsulated follicular variant of papillary thyroid carcinoma were identified in a review of all thyroid gland surgeries performed in 2002 within the Southern California Permanente Medical Group. All histology slides were reviewed and follow-up obtained. Seventy-five women and nineteen men, aged 20-80 years (mean 45.6 years), had a single (n=61), multiple (same lobe; n=20), or bilateral (n=13) tumor(s), ranging in size from 0.7 to 9.5 cm in diameter (mean 3.3 cm). Histologically, all cases demonstrated a well-formed tumor capsule, with capsular and/or lymphovascular invasion in 17 and no invasion in 77 cases. Lymph node metastases were not identified. The tumors had a follicular architecture, without necrosis or >3 mitoses/10 high-power fields (HPFs). Classical papillary thyroid carcinoma nuclear features were seen in at least three HPFs per 3 mm of tumor diameter, including enlarged, elongated, crowded, and overlapping nuclei, irregular nuclear contours, nuclear grooves, and nuclear chromatin clearing. Lobectomy alone (n=41), thyroidectomy alone (n=34), or completion thyroidectomy (n=19) was the initial treatment combined with post-op radioablative iodine in 25 patients. All patients were without evidence of disease after a median follow-up of 11.8 years. Encapsulated follicular variant of papillary thyroid carcinoma showed benign behavior, supporting conservative surgery alone and reclassification of these tumors to Noninvasive Follicular Thyroid Neoplasm with Papillary-like Nuclear Features (NIFTP).Modern Pathology advance online publication, 22 April 2016; doi:10.1038/modpathol.2016.65.
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relationship between thyroid and reproductive hormones
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an interesting and new aspect is the fact that both the coorelato ? FSH and TSH have a common second Myo - inositol dependent messenger. The increase in FSH typical of menopause could lead to a thyroid functional impairment related to a epimerase action induced .
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I'm considering doing a study to measure thyroid dose during neurointerventional procedures, using a biplane unit with an undercouch x-ray tube. Would the measurements done with a dosimeter on the neck over the thyroid be accurate? 
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There is a NaI-based scintillation dose rate meter (Model  SCINTO Thyroid) available from SEA, Germany. The detector is of spherical shape, suitable for the neck region covering the thyroid area very well. The technical pamphlet of the manufacturer gives a table showing estimation of expected thyroid dose for various measured doses (uSv/hr) for adults and children. Reference is provided for dose calculation.
For theoretical estimation of thyroid dose, a text book on Nuclear Medicing may be consulted.
Is this helpful? 
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I am interested in techniques to reconstitute follicles in vitro.
Thank you in advance.
Isabelle
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Hi Isabelle,
I did my PhD thesis working with reconstituted thyroid follicles. A lot of info you can find in my three first author papers but I would be happy share my experience too ;!
Is there something specific you wonder or have questions about?
Kind regards Camilla
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Can long term Lichen planus with thyroid leed to Obsessive-compulsive disorder
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Dear Dr Wajahat
i suggest to read this paper and abstract
Send to:
J Dtsch Dermatol Ges. 2015 Oct;13(10):991-9. doi: 10.1111/ddg.12781.
Obsessive-compulsive disorder in dermatology.
Mavrogiorgou P1, Bader A2, Stockfleth E2, Juckel G1.
Author information
Abstract
Patients with obsessive-compulsive (OCD) and related disorders - primarily trichotillomania, body dysmorphic disorder, and skin picking disorder - frequently present to dermatologists due to associated hair and skin symptoms. It is therefore crucial that dermatologists be familiar with these disorders. In this review article, we provide an update on clinical features, neurobiology factors, and treatment options for OCD spectrum disorders. Employing PubMed and Cochrane Library databases, a selective literature search was conducted using keywords related to dermatological disorders within the OCD spectrum. OCD and its related disorders share several phenomenological as well as pathophysiological similarities, thus warranting their classification within a separate nosological category of psychiatric disorders. Another similarity of OCD spectrum disorders is the frequent concurrence of hair and skin diseases. Besides symptomatic dermatological treatment, the combination of psychotherapy (behavioral therapy) and psychopharmacotherapy (SSRIs) may be helpful. Although recent insights into OCD have contributed to a better understanding and treatment thereof, more research is required, especially with respect to OCD spectrum disorders, for which large controlled treatment studies are still lacking.
© 2015 Deutsche Dermatologische Gesellschaft (DDG). Published by John Wiley & Sons Ltd.
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We are interested in animal models to evaluate thyroid abnormalities in rodents. 
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Thanks, This topic is not in my research area,
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I would like to undertake a thyroid treatment and monitoring assay in Xenopus tropicalis. I am new to using this is a s a model organism and would like to know if there are any classical landmark studies that have been undertaken in Xenopus sps. so I can get some background. Thank you.
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Hi,
I suggest you to check Barbara Demeneix on NCBI-PubMed. You may also be interested for this link.
Good Luck!
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patient is 28 male Caucasian. Incidental nodule 10X7 mm in right lobe, on FNA shows diagnostic image of papillary carcinoma. There is a 6.5X5mm cervical lymph node which shows "changed structure" on US. 
can lobectomy with dissection be sufficient for this case?  with future thyroid suppression therapy and under close monthly follow-up?
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Naftali Stern
Thank you very much for your detailed reply.
lymph node is described: sharply hypoechoic, nonhomogenic structure.
here are US images.
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TP53 and ATM tend to be highly expressed in cancer cells. Both of them function as dominant-negative tumor-suppressor. I have recently read the paper on the novel gene responsible for the familial thyroid papillary tumors (N Engl J Med 2015; 373:448-455). HABP2 G534E variant is also a dominant-negative tumor-suppressor gene and this is over-expressed in the familial thyroid cancer tissues, but not in thyroid papillary tumors. Surely, those genes can function predominantly as compared with normal gene product in the other allele, but I wonder why dominant-negative tumor-suppressor gene tends to be over-expressed in those tumors?
Link to publication:
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Many tumor suppressor genes are expressed in cancer cells (except deletions), but they are inactivated by multiple mechanisms such as phosphorylation, Ubiquitinations, protein interaction mediated sequestration and so on. I am not sure why you refer dominant negatives here.
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ELFA  or any other methods
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I think the best are immunoradiometric methods, , but labs use chemioluminiscence techniques.
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Do you consider first thyroglobulin level for radioiodine dose decision?
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Controversy exist in this issue until large randomized trials with long term follow up was done. The dormancy of thyroid cancer makes work on this issue very difficult. You may have recurrences even 35 years after initial therapy. Anyhow, the proponents of 30mCi emphasis on complications of radio-iodine(adverse effect on salivary gland, lacrimal gland,...), radiation burden, admission costs to the patients and absence of superiority of 100mCi which is shown in the two well known published trials by Schlumberger and Mallick in NEJM. The opponents of 30mCi on the other hand, mainly emphasis on the short term follow up of those studies as well as absence of well controlled studies about complications of I-131. A meta-analysis in 2012 (ANTONIS VALACHIS, Acta Oncologica, 2012) showed that successful ablation is not different between 30 and 100 mCi, while complications are significantly higher in high dose group. ION study which is undergoing, compares iodine administration versus no Iodine in low and low to intermediate risk patients. We should wait for its results that is expected to be published next year.
I treat all patients with low risk(ATA classification) with 30mCi. Also we are running a randomized trial in intermediate risk patients comparing 30mCi Vs 150 mCi ( Young T2 N1 and T3N0 with low fTg and noninvasive histology).
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Considering the need for discontinuation of Levothyroxine before imaging.
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I do not use WBS routinely, I rely on Tg and high resolution USG
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In some cases tg is low and Anti-Tg is abnormally high.
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If anti tg level is rising, yes.
In some patients with undifferentiated PTC, yes. (eg. at first presentation, WBIS showed LN or distant metastasis with ,low tg level. So, in this patient follow up: tg level is not reliable.)
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Has anybody experience with cardioversion during thyroid surgery with intraoperative continuous neuromonitoring via endotracheal tube electrode?
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Today, patients are sicker than 20 years ago and we still find more devices inside a patient. I t was not the question to avoid surgery, but still what to do if you need defibrillation during surgery - by internal or external device. Surgery without preparation of the recurrent nerve is not state of the art anymore despite a controlled randomized study of B. koch during the 90-ties in Germany, which demonstrated no differenc between  visualizing the nerve or not in subtotal resection or in hemithyreoidectomy.
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Medullary thyroid carcinoma
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Dear Mohamed
We suggest you to perform a completion thyroidectomy with a central neck dissection if the medullary is a sporadic one.
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We are observing an increase in the incidence of malignant thyroid lesions in recent years in our clinical practice. Is this our individual observation, or the observation of the mass?
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The reasons behind why the incidence of thyroid cancer is rising substantially are difficult to account for.  Increased use of diagnostic imaging capable of exposing subclinical disease is considered the most parsimonious explanation for this reported rise. The location of the thyroid gland places it within the window of many diagnostic-imaging studies. In addition, cross-sectional imaging studies have contributed to a 2.4-fold increase in the reported incidence of thyroid nodules over the past 30 years. 
The use of ultrasound for the screening of thyroid cancer has also been considered as a contributing factor.  This is believed to be the key factor in South Korea’s abrupt increase in thyroid cancer incidence.  A study based on the 2009 Korean National Cancer Screening Survey revealed that 13.2% of South Koreans undergo thyroid cancer screening with ultrasound. The link between imaging studies and increased incidence is supported by a correlation with access to healthcare, and the incidence is rising more rapidly in countries where healthcare expenditure is driven by the private sector than the public.
Contrary to the hypothesis that diagnostic imaging is the main cause of the increased incidence of small thyroid cancer, the incidence of large thyroid cancers has not declined, and is also increasing.  Moreover, higher rates of aggressive PTCs are being detected, including those with extrathyroidal extension and distant metastases.
Risk factors, not yet identified, may also be contributing to this increase in incidence.  Studies have also suggested that this may be due to high levels of ionizing radiation exposure. Moreover, hormonal, nutritional, and menstrual and reproductive factors may be causing this surge of incidence. The worldwide rise as well as the differing rates of thyroid cancer between countries suggests multiple factors may have a role in the incidence and warrant further investigation.
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We have encountered few cases of FNAC reported as anaplastic carcinoma, with patient presenting with symptoms of upper airway obstruction. What is your experience in managing such cases?
What is your experience with false positive anaplastic carcinoma on FNAC, which after thyroidectomy came back as non-anaplastic ie differentiated thyroid carcinoma?
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Yes-that is exactly what I suggest.
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I am trying to express thyroglobulin (TG) in FRTL-5 cells and subsequently pull it down by immunoprecipitation.
The cells are cultured in Coon’s medium supplemented with 2mM Glutamine + 10μg/ml Insulin + 10nM Hydrocortisone + 5μg/ml Transferrin + 10ng/ml gly-his-lys acetate + 10ng/ml somatostatin + 5% Foetal Bovine Serum (FBS) + 10mU/ml TSH.
After attempted immunoprecipitation of TG in FRTL-5 cells lysate using an anti-TG antibody, SDS-PAGE shows a single clean band (around 240kDa). However, this turns out in fact to be myosin (determined by proteomic analysis), and no trace of TG is observed.
  • Would anyone have tips or advice to improve TG expression in cultured FRTL-5 cells?
  • Since my antibody seems to have specificity issues, could anyone recommend a reasonable antibody for the immunoprecipitation of TG in cell lysate ?
Many thanks in advance
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The MW of Tg is greater than 240, thus your band is probably not Tg. A good antibody was from dako (it was very good in immunhistochemistry and Elisa). With 10mU TSH, you must have an expression of thyroglobulin.
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It is general knowledge that secondary glaucoma due to thyroid orbitopathy is of the open angle type (compressive causing decreased outflow and increased episcleral venous pressure)
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Dear colleagues,
eyes with primary angle closure suspect (and its consequences) remain frequently undectected, because gonioscopy is often not performed or not performed correctly. Hence this condition is largely underreported, except for the studies done in Asian subjects, and the occurence in a patient with thyroid orbitopathy is unlikely to be more than purely coincidental. (And if it were not, it would by definition not be 'primary' anymore.)
Thyroid orbitopathy can lead to increased IOP (be sure to perform the differential pressure test to eliminate the effect of inferior rectus muscle fibrosis), as a result of increased intra-orbital pressure, as stated above. This pressure pushes the eye outwards the orbit (in the best case), but is not expected to alter the anatomy of the anterior segment.
The event of a choroidal effusion is a well known cause of secundary angle closure. However I am unaware of such a link with Thryoid orbitopathy, in spite of a search on pubmed.
The usually impressive clinical picture of orbital congestion termed 'malignant' thyroid orbitopathy, with its potential for associated vision loss due to optical nerve compression (and/or corneal damage) will in most instances lead to therapeutic intervention, eliminating the potential for intra-ocular vasculair complications and hence the potential for neovacular glaucoma.
This being said, a recently published case report demonstrates the potential for intra-ocular vascular complications exists, hence its potential complications as well. (see: A patient with branch retinal vein occlusion accompanied by superior ophthalmic vein thrombosis due to severe superior ophthalmic vein enlargement in a patient with graves ophthalmopathy. Park HS et al., 2014)
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There is a tendency among doctors to assess thyroid function, i.e. hypo- and hyperthyroidism simply by measuring TSH. It is argued that clinical scores are complicated, difficult to obtain and imprecise. Notwithstanding the ongoing discussion of the "true" reference range for TSH, mere evaluation of a laboratory value will falsly classify 3% of euthyroid persons as either hypo- or hyperthyroid, as their TSH values will be outside the 97% normal range - assuming Gaussian distribution. On the other hand, patients report better quality of life when they are "on the edge of hyperthyroidism" although this - subclinical hyperthyroidism - is a known risk factor for cardiac arrhythmias and osteoporosis. Is there a simple way to assess thyroid function, maybe with questions about heat and cold intolerance, being tired or nervous and loss or gain of weight? Has some such score been evaluated in a study of long-term health effects of thyroid function?
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To my knowledge there is no study using a score for thyroid dysfunction and long-term outcome. The main problem is, as you mentioned, that most of those studies mainly measured TSH only once. There is an unfortunate misunderstanding concerning the normal range of TSH. Reference values are misinterpreted with the normal range. Whereas in a normal population the reference values for TSH is between 0.3 and 2.5 or even 0.2 and 2.1, this does not mean that individuals with a TSH of 3.6 mU/L are subclinical hypo as long as FT4 is within the normal range. In individuals with a TSH up to 4 mU/L nearly 100% have normal FT4 levels. The proportion of those with a low FT4 increases slightly,  when TSH is > 4 mU/L. Therefore the normal range for TSH is between 0.4 and 4 mU/L and this normal range is different from the reference values of a certain population.
For the clinical practice therefore the simply TSH measurement and classification only on this TSH level is not sufficient. But of course the history of the patient and specific complaints always have to be considered. It would be helpful to have a score system, but because the signs and symptoms of hypo- as well as hyperthyroidism are unspecific, this will not be easy to establish. Therefore the experience of the physician together with the lab test  results are still necessary for diagnosis and treatment of patients.
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Thyroid exophthalmos
Proptosis ( Unilateral vs Bilateral)
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Racial variation in exophthalmometry values is observed while comparing normative values. Dunsky and later Migliori & Gladstone report the mean exophthalmetry in normal African-American population to be 18.2 and 18.56 mm respectively. Quant & Woo have reported the mean value in Asian population to be 16.73 mm. Migliori & Gladstone report the value among Caucasians to be 16.55 mm. As you have mentioned, Sodhi et al. in their study in the Indian population have reported a range of exophthalmometric values in a normal Indian population aged 3-80 years was 7-19 mm for males and 7-21 mm for females. I would tend to agree that the general Indian population has a mean exophthalmometry reading of 19 mm. WIth regards to abnormal values, any value above 21 mm or a difference of 2 mm or more between the readings of the right and left eye should arouse suspicion in cases of unilateral proptosis. Hope this helps.  
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Many drugs and metal ions in the plasma reduces the incidence of hormonal secretions i.e. Calcium supplements (Ca-citrate) can reduce the parathyroid secretion by 50 % more than the carbonates by PTH suppression. Can we think of this type of different medication strategy for cost effective manner only for the lower extent of suppression if needed?
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many drugs are used without thinking about their relation with brain structure. For example Beta blokers are used for effect on the heart, but some Beta receptors are in the brain. this relation is\in my opinion\ reson for centisises of receptors and problems with chronic situations. cost effective results are comming because we do not understand this relations and we are to brave in use the same medicines for a long time.
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If follicular thyroid adenomas are premalignant lesions, we can regard them as benign tumor, and lobectomy is enough.
If follicular thyroid adenomas are carcinomas in situ, how to deal with them?
To the contrast, is there any evidence show that follicular thyroid adenomas are real benign that do not progress to carcinoma?
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It is likely that follicular carcinomas arise from preexisting follicular adenomas, so that some follicular adenomas may be carcinomas in situ. This adenoma to carcinoma pathogenesis is reminiscent of the well-accepted colonic tubular polyp to colon cancer transition. Because diagnosis of a thyroid follicular adenoma requires complete excision of the entire lesion (to see if there is vascular or capsular invasion), most appropriately in the context of an ipsilateral total thyroid lobectomy, the failure to see residual or metastatic disease from such lesions is equally consistent with a benign adenoma or a carcinoma in situ.
Unfortunately, this academic distinction becomes of concern regarding efforts to distinguish these tumors by FNA biopsy using gene profiling or assessment of specific markers, such as telomerase, to avoid thyroid surgery... If not resected, would such adenomas evolve into carcinomas? To date, we don't know exactly.
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NTIS nonthyroidal illness syndrome.
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I have no experience on this issue. What is known is that about 15% of patients with hypothyroidism would do better with the combination of L-thyroxine and Tiiodothyronine once they have diminished capacity to transform T4 into T3, due to deficient type 2 deiodinase activity.  
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Is it linked to vasoconstriction? What are the consequences? 
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Maybe the sympathomimetic effect in hyperthyroidism which can lead to tachycardia and hypertension.
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The role of elastography for better diagnosis of thyroid nodules is controversial and the technique used different. Do you use elastography in the Routine diagnosis of thyroid nodules? Which characteristics are useful?
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According to our observations US elastography has great importance in the selection suspect nodules for FNAB indication.  With  a high prevalence of nodules makes it difficult to use FNAB in every nodule
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MILLIPLEX MAP Rat Thyroid Magnetic Bead Panel using Luminex.
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Verify that your pipettes are working properly, that multi channel pipettes are consistent between channels, that you equilibrate your tips with whatever you are pipetting by  wetting the tip. Verify your technique. The smaller the volumes, the more careful you need to be.
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The premise at the top of your study, "Consumption of high-fat foods is one of the major causes of obesity," seems to me to be something that's been up for debate for some number of years now, with people actually losing weight on high-fat/low-carb diets. Is there significant evidence that you could cite that supports this claim? If this is your assumption on the outset, doesn't that naturally skew the parameters of the study?
Aren't many obese people who consume high amounts of fat also impacted by other factors, such as thyroid disruptors in the environment; the excess of omega-6 oils in most packaged foods, high-carb + high fat diets, and sedentary work in temperature controlled environments?
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Dear Ruby,
thank you so much for mentioning to a fine point. yes I agree with you, there is a controversy about obligatory relation between high fat diet and obesity. There are some situations which do not confirm it. But note that, calorie intake and over weight/obesity is a fact. Calorie content of lipids are high. So if you do not interfere in calorie intake (such as accompany high fat with low carb) it will cause over weight/obesity. So in control conditions such as animal study, high fat diet can cause over weight/obesity. As we encountered to this in rat control group which fed only by high fat diet. I attached two papers which mentioned to high fat diet as a cause of obesity and also know there are papers against it too. But we know about a controversy subject we can not refuse or confirm each side and have to wait for increase documents in one side in future. Any way thank you so much again for your time, curiosity and precision, I will refer your comment to the author correspondence, and will consider it in next publication.
best
mehdi
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Specifically an MRI showing the thyroid gland and neighboring structures of the neck. I am in need for MRI images of a swine to identify the structures of the neck.
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This could be what you are looking for:
Neuroimage. 2001 Nov;14(5):1089-96.
MR-based statistical atlas of the Göttingen minipig brain.
Watanabe H1, Andersen F, Simonsen CZ, Evans SM, Gjedde A, Cumming P; DaNeX Study Group.
Just in case you have to switch to canine:
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Had a problem with a patient recently
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We performed a systematic review of the existing literature in 2012 (Genovese and Noureldine et al. Ann Surg Oncol 2012) and examined 4,546 patients who underwent surgical resection for Graves' disease (3,158 patients had subtotal thyroidectomy and 1,388 had total thyroidectomy).
Of the patients that underwent subtotal thyroidectomy, 330 (10.4%) had persistent or recurrent hyperthyroidism. While only 4 (0.3%) patients who underwent total thyroidectomy had persistent or recurrent hyperthyroidism.
In the studies analyzed, the rate of permanent recurrent laryngeal nerve palsy in patients who underwent subtotal thyroidectomy ranged from 0-1.9%. There were no reports of transient recurrent laryngeal nerve palsy. In patients who underwent total thyroidectomy, the rate of permanent recurrent laryngeal nerve palsy ranged from 1.5-11.1%, and the rate of transient nerve palsy was 1.3-7%.
You can also read the meta-analysis by Palit et al. (palit T et al. J Surg Res, 2000), contrasting total versus subtotal thyroidectomy, as they have showed no significant difference between complication rates of total thyroidectomy and lesser resections. The rate of permanent recurrent laryngeal nerve palsy was 0.9% after total thyroidectomy and 0.7% after subtotal thyroidectomy, for those studies when nerve function was reported. Transient hypocalcemia occurred in 9.6% and 7.4%, respectively. Interstingly, permanent hypoparathyroidism occurred in 0.9% of patients after total thyroidectomy and in 1.0% after subtotal thyroidectomy. Total thyroidectomy was also found to have higher cure rates and negligible recurrence rates.
Initially, subtotal thyroidectomy was advocated as the standard surgical treatment for Graves' disease due to the assumed lower risk of complications, compared to total thyroidectomy, and the possibility of avoiding hormone replacement therapy. However, given that subtotal thyroidectomy provided an unpredictable outcome with regard to ultimate thyroid hormone levels and that the risk of permanent complications was no greater than with total thyroidectomy, there appear little logical reason to continue recommending subtotal thyroidectomy for the surgical management of GD.
Also, you can read Kandil, Noureldine et al. Surgery 2013, Surgery for Graves disease is associated with a higher risk for complications when performed by less experienced surgeons. Graves disease was not a significant predictor of postoperative complications when performed by high volume surgeons. Hospital volume had an inconsistent and marginal protective effect on postoperative outcomes.This finding should prompt recommendations for increasing surgical specialization and referrals to high-volume surgeons in the management of Graves disease.
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Thyrotoxicosis causes an increase in metabolic activity but a decrease in menstruation, what is the process behind the Amenorrhea?
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Hyperthyroidism commonly results in the increased levels of the sex hormone-binding globulins, which in its turn might lead to the increased plasma estrogen levels, level of circulating androgenes as well are increased, LH levels are high, though lacking LH peaks.
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On the one hand, several studies have shown that the V600E-BRAF mutation is closely related to high-risk clinicopathological factors and poorer outcome of PTC. This suggests that this mutation should be considered as a poor prognostic marker in PTC, which may lead to better management of individual patients.
On the other hand, several studies have demonstrated that BRAF mutation testing of thyroid fine-needle aspiration specimens enhances the predictability of malignancy in thyroid follicular lesions of undetermined significance, which are known to have an excellent prognosis.
Some authors in their publications have underlined this contradiction. It is important that a resolution of this contradiction be determined.
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This is an interesting question and an actual matter of debate but to my mind, there is no contradiction between these 2 assertions.
BRAF mutation is present in around 40% of papillary thyroid carcinomas and never in benign lesions. In patients with thyroid nodules, FNA spécimens give an indeterminate result in 20 to 30% of cases and these patients are often operated although the lesion is benign in most cases. It is, thus, important to improve the performances of FNA. BRAF determination on FNA specimens may contribute since when a BRAF mutation is identified, this ensures the diagnosis of PTC. By contrast, when the analysis is negative, a cancer cannot be ruled out. Research is, now, focusing on the identification of molecular sets allowing better discrimination between malignant and benign diseases.
Papillary thyroid carcinomas are usually of good prognosis with an overall survival of 95% at 10 years but it is estimated that 3 to 5% of patients die from their cancer and that 10 to 20% have a recurence. There is a debate on the prognosis value of BRAF mutation. It has been reported that thyroid cancer with a BRAF mutation are more agressive, with frequent extra-thyroidal extension and FDG PET avide lesions. However the impact of BRAF status on patient's outcome is not fully determined. Moreover, it is not demonstrated that extensive lymph-node dissection improves post-operative outcome in such patients.
This is an active research field and more definite responses are expected in the next few years