Science topic

Dementia - Science topic

An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness.
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📣 Open Call for Papers 📣
We invite you to submit your research or review papers by December 31, 2024 to be considered for an upcoming special issue of Alzheimer's & Dementia (Alzheimer's Association®). This issue will honor the 40th anniversary of the National Institute on Aging (NIA)'s Alzheimer's Disease Research Centers Program and the 25th anniversary of the National Alzheimer's Coordinating Center!
Learn more and submit your article here: bit.ly/AD_Special_Issue
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  • Submission Deadline: December 31, 2024
  • Research or review papers will be accepted.
  • All papers will be reviewed according to the journal's policies, procedures, and publishing fees.
  • The final collation of this issue is expected in Fall 2025.
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How can I prove the dementia rat model?
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A very common Invivo experiment model which you could consider in studying dementia is the scopolamine-induced cognitive impairment model. Scopolamine, a muscarinic receptor antagonist, impairs cholinergic function, leading to atrophy and degeneration of brain neurons in rats. It is administered intraperitoneally (IP) once daily for 7-14 days.
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need to review articles on care giving in dementia and challenges faced
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Here are references to recent studies on protective factors and resilience in caregivers of individuals with dementia:
1. **Martyr, A., Rusted, J. M., Quinn, C., et al. (2023).** *Resilience in caregivers of people with mild-to-moderate dementia: findings from the IDEAL cohort.* BMC Geriatrics, 23, Article 804.
- This study explored various factors associated with resilience among caregivers, identifying key sociocultural, contextual, and psychological elements that contribute to caregiver resilience.
- [Link to Study](https://doi.org/10.1186/s12877-023-04549-y)【13†source】【14†source】
2. **Quinn, C., Morris, R. G., & Clare, L. (2023).** *Personality traits, self-efficacy, and competence in dementia caregiving.* Journal of Geriatric Psychiatry.
- This article examines how personality traits and self-efficacy influence caregiver competence and resilience, providing insights into the psychological dimensions of caregiving.
3. **Bradford Scholars Repository. (2023).** *Resilience in caregivers of people with dementia: findings from the IDEAL cohort.*
- This open-access repository provides additional data and analysis from the IDEAL cohort, focusing on how caregiver characteristics and care demands influence resilience.
- [Link to Study](http://hdl.handle.net/10454/19726)【14†source】
These references should provide you with a comprehensive understanding of the current research on resilience in dementia caregivers.
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Following is the aspect of Dementia care. how can we set benchmark for these?
  • support and co-ordination in transition of care within health care facilities.
  • screening of undiagnosed with dementia symptoms.
  • Management of person with Dementia with BPSD.
  • Delirium screening
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The process of establishing benchmarks in dementia care requires multiple processes that prioritize enhancing quality and measuring performance. Here is a framework that can assist you in setting up these benchmarks: Internal benchmarking refers to the process of comparing an organization's performance against its own previous performance or against the performance of other departments within the same organization. This practice helps identify areas of improvement and best practices that can be implemented to enhance overall
1. Define Key Performance Indicators (KPIs): - Determine precise KPIs that accurately measure the quality of care provided to individuals with dementia. Examples encompass many metrics such as patient well-being scores, staff-to-patient ratios, incident rates (such as falls and prescription errors), and patient satisfaction surveys.
2. Acquire Data: - Compile data pertaining to the identified Key Performance Indicators (KPIs) within a specified timeframe. Possible methods for gathering information may involve conducting chart reviews, obtaining feedback from staff members, and monitoring incident reports.
3. Data Analysis:- Evaluate the gathered data to detect trends, patterns, and areas that require enhancement. Analyze and evaluate the performance of various units or teams within your organization. 4. Establish Performance Targets:- Utilizing the analysis, define precise and quantifiable objectives for enhancement. For example, you may set a goal to decrease the rate of falls by a specific percentage throughout the upcoming year. 5. Execute Modifications: - Formulate and execute strategic plans to accomplish the established objectives. This may entail staff training, policy amendments, or the implementation of new care protocols. 6. Monitor Progress: - Consistently evaluate the Key Performance Indicators (KPIs) to determine if the established benchmarks are being achieved. Modify strategies as necessary according to continuous data analysis. External benchmarking refers to the process of comparing an organization's performance, practices, or outcomes with those of other external entities in order to identify areas for improvement or to measure performance against industry standards. 1. Conduct Research on Best Practices: - Engage in research to gain an understanding of the most effective methods and standards employed by other organizations in the field of dementia care. This may involve conducting a thorough examination of relevant literature, examining guidelines provided by reputable health organizations, and engaging in partnerships with hospitals or care facilities renowned for their exceptional dementia care. 2. Choose Comparison Organizations: - Select organizations or programs that are similar in size, population served, and services provided to use as benchmarks. 3. Gather Comparative Data: - Acquire data on their performance indicators pertaining to dementia care. Examples of this could encompass published reports, surveys, or involvement in benchmarking consortiums.
4. Evaluate and Compare: - Examine the external data and contrast it with your internal measures. Identify deficiencies in healthcare or inconsistencies in performance and areas where your company thrives. 5. Establish External Benchmark Objectives: - Utilizing the comparative analysis, modify your internal objectives to correspond with or beyond the criteria established by the external benchmarks. 6. Execute and Fine-tune: - Similar to internal benchmarking, utilize the knowledge acquired from external benchmarking to guide adjustments and enhancements in practice. Observe and evaluate these alterations to determine their long-term effects.
In conclusion Establishing standards in dementia care necessitates a methodical strategy that encompasses the identification of pertinent indicators, data gathering, analysis, and continuous monitoring. By integrating both internal and external benchmarking, healthcare providers can gain a deeper understanding of their performance and actively work towards ongoing enhancement in the quality of care they deliver. Involving stakeholders, such as families and caregivers, can further strengthen the benchmarking process and improve the quality of care.
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Hello everyone,
I am currently exploring several options to give the collected data the greatest value possible.
I have demographic data on older people, where I perform various memory and mood tests. The previous hypotheses were the following:
  • Drawing out the difference between dementia and depression.
  • Identify if the digital tool is as effective as the classic one
  • Contributing to the data collected as a predictor of dementia
A few years ago, studies talked about the real possibility of predicting some years before, what your future mental health will be in terms of memory.
Do you think there is any way to provide value in that sense, with demographic data, clinical tests like MoCa, Yesavage, Lawton, MFE?
Here you are some of these studies.
Study of the brain through images:
  • Jagust, W. (2018). Images of the evolution and pathophysiology of Alzheimer's disease. Nature Reviews. Neuroscience, 19(11), 687–700. doi:10.1038/s41583-018-0067-3.
Analysis of biomarkers in cerebrospinal fluid or blood:
  • Hampel, H., O'Bryant, S. E., Castrillo, J. I., Ritchie, C., Rojkova, K., Broich, K.,… Lista, S. (2018). PRECISION MEDICINE – The golden door for the detection, treatment and prevention of Alzheimer's disease. Journal of Alzheimer's Disease Prevention, 5(4), 243–259. doi:10.14283/jpad.2018.29.
Genetic studies:
  • Karch, C. M., and Goate, A. M. (2015). Alzheimer's disease risk genes and mechanisms of disease pathogenesis. Biological Psychiatry, 77 (1), 43–51. doi:10.1016/j.biopsych.2014.05.006.
Cognitive evaluations and neuropsychological tests:
  • Amariglio, R. E., Becker, J. A., Carmasin, J., Wadsworth, L. P., Lorius, N., Sullivan, C.,… Sperling, R. A. (2012). Subjective cognitive complaints and amyloid burden in cognitively normal older people. Neuropsychology, 50(12), 2880–2886. doi:10.1016/j.neuropsychologia.2012.08.011.
With python and with sk-learn is a best way to start?
Which features are the more relevants to add value to the prediction?
Thanks in advance,
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Thanks Adnan Majeed ,
There are important ethic considerations as you mention.
In our use case, the digitalized clinical tests, dementia and depression test, are administered. We use Alexa devices to pass these tests so that the information is digitized, obtaining the answer of the final score automatically.
Taking into account the data collected from our users, the features to clasify them will be:
  • Demographic Data
  • Behavior patterns
  • Their answer to the clinical test
  • Voice Data or voice patterns
  • Gesture patterns
My proposal is to compare the digitized test with the classic one to check the sensitivity and specificity. And compare these two terms with the ones I get when I add the Machine Learning layer. Probably the library I use is Scikit-learn.
Do you think I'm on the right path? Are there any important suggestions to keep in mind?
Thanks in advance,
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The effects of the menopause and hormone levels in women have been associated with cognitive decline (Tsolaki M et al. 2005).
The fact that women are more likely to have cognitive deficits than men is an important factor (Laws KR, 2018). Considering the reproductive endocrinology of both males and females, where women experience an increase in follicle stimulating hormone (FSH) in response to low levels oestrogen in the hypothalamic-pituitary-adrenal (HPA) axis feedback loop. Most men continue to produce testosterone throughout life and do not experience this increase in FHS to the same extent as females. However, when low levels of testosterone do occur FSH must be increased due to the HPA axis feedback and low testosterone is associated with dementia in men (Yeap BB, 2011).
Some studies reveal that FSH levels and dementia show that there is an association between increased level of the hormone and loss of cognitive function, in animal studies. Interestingly, FSH blockers have been shown to reduce cognitive decline in one study (Xiong J et al 2022).
A recent study reported that men who use Sildenafil for erectile dysfunction have been associated with a decrease in susceptibility to Alzheimer’s disease (Huo X, 2023). Sildenafil (Viagra) increases testosterone levels in men, thus the FSH should also be reduced (Spitzer M, 2013). Has this aspect of FSH levels and susceptibility to dementia been investigated?
A systemic review investigated the use of sildenafil for Alzheimer's patients and recommends a repurposing of the drug for patients with dementia (Sanders O, 2020).
Could the above discussion of endocrinology be a partial explanation for the effects of Sildenafil and reduced incidence of dementia in men who take the drug and should further investigation take place into this aspect of endocrinology and dementia?
  • Laws KR, Irvine K, Gale TM. Sex differences in Alzheimer's disease. Curr Opin Psychiatry. 2018 Mar;31(2):133-139. doi: 10.1097/YCO.0000000000000401. PMID: 29324460.
  • Tsolaki M, Grammaticos P, Karanasou C, Balaris V, Kapoukranidou D, Kalpidis I, Petsanis K, Dedousi E. Serum estradiol, progesterone, testosterone, FSH and LH levels in postmenopausal women with Alzheimer's dementia. Hell J Nucl Med. 2005 Jan-Apr;8(1):39-42. PMID: 15886752.
  • Yeap BB, Flicker L. Testosterone, cognitive decline and dementia in ageing men. Rev Endocr Metab Disord. 2022 Dec;23(6):1243-1257. doi: 10.1007/s11154-022-09728-7. Epub 2022 May 28. PMID: 35633431; PMCID: PMC9789006.
  • Xiong J, Kang SS, Wang Z, Liu X, Kuo TC, Korkmaz F, Padilla A, Miyashita S, Chan P, Zhang Z, Katsel P, Burgess J, Gumerova A, Ievleva K, Sant D, Yu SP, Muradova V, Frolinger T, Lizneva D, Iqbal J, Goosens KA, Gera S, Rosen CJ, Haroutunian V, Ryu V, Yuen T, Zaidi M, Ye K. FSH blockade improves cognition in mice with Alzheimer's disease. Nature. 2022 Mar;603(7901):470-476. doi: 10.1038/s41586-022-04463-0. Epub 2022 Mar 2. PMID: 35236988; PMCID: PMC9940301.
  • Huo X, Finkelstein J. Using Big Data to Uncover Association Between Sildenafil Use and Reduced Risk of Alzheimer's Disease. Stud Health Technol Inform. 2023 May 18;302:866-870. doi: 10.3233/SHTI230291. PMID: 37203519.
  • Spitzer M, Bhasin S, Travison TG, Davda MN, Stroh H, Basaria S. Sildenafil increases serum testosterone levels by a direct action on the testes. Andrology. 2013 Nov;1(6):913-8. doi: 10.1111/j.2047-2927.2013.00131.x. Epub 2013 Sep 18. PMID: 24106072; PMCID: PMC6036338.
  • Sanders O. Sildenafil for the Treatment of Alzheimer's Disease: A Systematic Review. J Alzheimers Dis Rep. 2020 Apr 22;4(1):91-106. doi: 10.3233/ADR-200166. PMID: 32467879; PMCID: PMC7242821.
https://www.bbc.co.uk/news/health-68232649 (Radio 4 Today programme report 8.2.24)
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Further to this line of thinking about the relationship between hormone levels and dementia, could the GnRH increases associated with FSH increased levels also be an important factor? When considering the chicken or the egg in this pathogenesis, could GnRH have a hormesis effect on neurone where low levels are functional but high levels have a pathogenic effect when levels cross a certain threshold of expression?
A recent study reported an association in midlife women where elevated gonadotropin levels are associated with increased biomarker risk of Alzheimer's disease.
One study in mice indicated an association with the HPG axis and cognitive senescence with a suggestion that pharmaceutical intervention reducing GnRH could reduce the pathophysiological processes underlying AD and plaque formation.
  • Nuruddin S, Syverstad GH, Lillehaug S, Leergaard TB, Nilsson LN, Ropstad E, Krogenæs A, Haraldsen IR, Torp R. Elevated mRNA-levels of gonadotropin-releasing hormone and its receptor in plaque-bearing Alzheimer's disease transgenic mice. PLoS One. 2014 Aug 4;9(8):e103607. doi: 10.1371/journal.pone.0103607. PMID: 25089901; PMCID: PMC4121068.
  • Nerattini Matilde, Rubino Federica, Jett Steven, Andy Caroline, Boneu Camila, Zarate Camila, Carlton Caroline, Loeb-Zeitlin Susan, Havryliuk Yelena, Pahlajani Silky, Williams Schantel, Berti Valentina, Christos Paul, Fink Matthew, Dyke Jonathan P., Brinton Roberta Diaz, Mosconi Lisa, Elevated gonadotropin levels are associated with increased biomarker risk of Alzheimer's disease in midlife women, Frontiers in Dementia, 2, 2023 https://www.frontiersin.org/articles/10.3389/frdem.2023.1303256 DOI:10.3389/frdem.2023.1303256
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Dementia:
A ticking time bomb for all over 50 year olds.
50% of 85 year olds have dementia...Bill Gates's dad has condition & so more money from Gates.
every 3-4 minutes someone gets dementia
PDE type 4 inhibitors protect endothelial cells & increase cerebral blood flow. But emetic side effects for Rolipram pre-clinically.
Cilostazol trial underway for 2 years.
wii & Konnect gaming thought to slow down dementia
what is the answer to todays sufferer's of dementia?
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An active mind
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Estoy realizando un Trabajo Fin de Grado de Enfermería al respecto de este tema.
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Muchas gracias, Berna!
Estaba investigando esta línea: La demencia no afecta únicamente a las células del cerebro, sino que también causa cambios en otros sistemas del cuerpo, como la piel. Los tejidos de la piel y del cerebro provienen de las mismas células madre embrionarias y pueden experimentar el mismo tipo de degeneración. A partir de este hallazgo, se está desarrollando una prueba para identificar un biomarcador que indique la densidad celular anormal en la piel de pacientes con demencia, ya que se ha observado que son más propensos a sufrir heridas.
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Here is a new terminology I came across and that is psychobiotics which is being researched widely for their effect on lowering the episodes of anxiety and dementia. Please enlighten me about the same and also about the bacterial species that are of significance for the same.
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How do I invite them as newcomers to the system they are
Sheryl Zimmerman, PhD Sheryl Zimmerman <Sheryl_Zimmerman@unc.edu>
and Phillip Sloane, MD Philip Sloane <philip_sloane@med.unc.edu>
Also I am part of two separate research teams one is Duke University the other is
UNC@Chapel Hill both are doing two totally different approaches of oral care for persons with dementia and AD is there any way my account could be fixed for the two separate reams i belong to.
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Click your account (your profile pic. at top right corner) -> "Invite colleagues" -> enter their email addresses and "Send nomination".
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Dementia affects several millions of people across the world. There are various types of dementia and Alzheimer’s disease is the most common type. This disease that is yet to have a cure affects several millions of families in several different ways.
Dementia is a global crisis, perhaps we can call it the dementia pandemic! Dementia is everyone's problem and as a result, we must take the responsibility to look after ourselves. One of the easiest ways to support people living with dementia and their caregivers is to be aware of this disease and by so doing we probably can become a little bit more compassionate and dementia-friendly.
Most people living with dementia receive care from their immediate family members or friends and neighbours. This makes informal caregivers become isolated. They become what we call the invisible patients. Most people who provide informal dementia care are female caregivers mainly spouses, female adult children, family members, friends, and neighbours.
Dementia caregivers suffer equally as they are mostly available to provide the required care for their family members who are living with dementia. Informal caregivers suffer from several conditions such as physical and psychological challenges,
loss of job/livelihoods = financial problems, and loss of social life such as their hobbies. Among other challenges, informal caregivers suffer from stress, anxiety, and depression.
How dementia-friendly are you and how dementia-friendly are your localities?
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I must express my heartfelt thanks to you all who have been contributing to this discussion so far. Thank you so much, Ljubomir Jacić Mary C R Wilson Sundus F Hantoosh Mauro Colombo Anamitra Roy
Best regards
Muhammad
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Hi fellow geeks, I am trying to understand the various statistical methods/tools used for studying risk factors associated with dementia especially the 40% of modifiable risk factors(Dementia prevention, intervention, and care: 2020 report of the Lancet Commission).
A recent article (PMID: 36394871) demonstrated the use of Least absolute shrinkage & selection operator and multivariate Cox proportional hazards regression models.
And a previous work (DOI: 10.1002/alz.12802) Bayesian regression modeling & Regression analysis over time prior to diagnosis.
Looking at these, I see it as using different tools on a swiss knife to get the job done... So if I were to design a specific tool and test it out...
How do I go about it?
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Rana Hamza Shakil
Given the subjective nature of dementia, each of the tools/techniques you have mentioned would be to be carried out individually, right?
In that case, that would require individual data collection and curation.
Which translates into hardware and personal time requirements/allocation.
How does one solve this challenge then?
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Erythropoietin (EPO) levels were significantly lower in critical and deceased Covid-19 patients:
Suggested treatment for both Covid-19 and LongCovid: rhEPO :
Signs, symptoms and co-morbidities in PostCovid indicate continued EPO deficiency:
Pathogenesis : the immune response to the virus is so strong (with inflammatory cytokines), that it damages the kidneys EPO production.
Inflammatory cytokines
TNF-alpha, IFN-gamma, IL1B, IL6, IL17A ... (etc.) all suppress EPO:
Figure 1:
arrow direction = "increase of". EPO treatment would move "Covid-19" to the right in the figure. It follows that too much EPO can be harmful - at the far right in the figure.
There could be further causes of EPO deficiency:
Obesity, diabetes and pain in the joints
Muscle pain, exercise intolerance, lack of energy and mitochondria
Aging
Accelerated biological aging in COVID-19 patients:
Accelerated ageing is associated with increased COVID-19 severity and differences across ethnic groups may exist:
Lack of energy - red blood cells
EPO regulates the lives and deaths of red blood cells.
The primary effect of EPO is increased number of red blood cells and thereby increased oxygen uptake, which is much needed in severe cases of Covid-19 - and in LongCovid.
EPO is the natural inhibitor of the Sphingomyelinase-Ceramide-Pathway :
(Hemoglobin is measured in gram per liter or deciliter blood. It says nothing about blood volume, how many liter of blood the patient has. There is a reason for, that LongCovid patients look pale and are tired).
Blood volume perturbations in the postural tachycardia syndrome
Differentiation of Prior SARS-CoV-2 Infection and Postacute Sequelae by Standard Clinical Laboratory Measurements in the RECOVER Cohort :
(The deficient phagocytosis (mentioned below) is further complicating blood measurements, as it means that debris from dead red (and white?) blood cells is floating around).
HDL-Cholesterol deficiency, lipids and thrombosis
EPO inhibits (/regulates) NF-kappaB and thereby reduce TNF-alpha:
Co-aministration of thrombolytic therapy and rhEPO should be avoided in treatment of stroke:
Complement system and Micro-amyloid-fibrinogen-clots
EPO regulates the Complement system:
The micro amyloid fibrinogen clots are yet another sign of erythropoietin deficiency in LongCovid :
And EPO treatment is how to get rid of them :
Decreased platelet activation through glycoprotein VI
Endothelial dysfunction and heart disease
Chronic stress, hypocortisolemia
... caused by EPO-deficiency, inflammatory stress and maybe corticosteroid treatment.
Erythropoietin negatively regulates pituitary ACTH secretion :
"Prolonged or exaggerated stress response may perpetuate cortisol dysfunction, widespread inflammation, and pain." :
Hair Loss
Brain fog and demyelinaton
As mentioned above ("Lack og energy - red bloodcells") is EPO essential for sphingomyelin, and the same goes for myelin:
Erythropoietin re-wires cognition-associated transcriptional networks:
Introducing the brain erythropoietin circle to explain adaptive brain hardware upgrade and improved performance :
Microglia activation and neuroinflammation
Brain erythropoietin fine-tunes a counterbalance between neurodifferentiation and microglia in the adult hippocampus:
An effective erythropoietin dose regimen protects against severe nerve injury-induced pathophysiological changes with improved neural gene expression and enhances functional recovery:
EPO prevents neuroinflammation and relieves depression via JAK/STAT signaling :
Depression and other mental disorders
Cognitive impairment in children
EPO is essential for brain development:
Blood-brain-barrier
Blood–brain barrier disruption and sustained systemic inflammation in individuals with long COVID-associated cognitive impairment:
The relationship between erythropoietin pretreatment with blood–brain barrier and lipid peroxidation after ischemia/reperfusion in rats
Erythropoietin protects against hemorrhagic blood–brain barrier disruption through the effects of aquaporin-4
Loss of or distorted taste
EPO is vital for the maintenance of both myelin and sphingomyelin.
Blindness
Inhibiting Ceramide synthesis preserves photoreceptor viability and functionality :
Hearing loss
EPO ↔ Melatonin ↔ Serotonin ↔ EPO --> dopamine
and insomnia
(they mutually increase one another)
Fatty liver
Alcohol intolerance
Kidney damage
Recombinant human erythropoietin reduces rhabdomyolysis-induced acute renal failure in rats
Erythropoietin protects against rhabdomyolysis-induced acute kidney injury by modulating macrophage polarization
Inflammation and lung tissue damage
(Not meaning that inflammation is only in lungs)
Erythropoietin inhibits respiratory epithelial cell apoptosis in a model of acute lung injury:
Erythropoietin inhalation enhances adult canine alveolar-capillary formation following pneumonectomy:
Autoimmunity
IgG antibodies and EPO resistance
Restrained memory CD8+ T cell responses favors viral persistence and elevated IgG responses in patients with severe Long COVID:
STAT5 Is Critical To Maintain Effector CD8+ T Cell Responses:
(article only selected for the headline)
Antibodies to Erythropoietin Are Associated with Erythropoietin Resistance in Hemodialysis Patients in KwaZulu-Natal (South Africa): https://journals.lww.com/sjkd/fulltext/2020/31050/antibodies_to_erythropoietin_are_associated_with.4.aspx
CD8+ T cells and activation of T-cell receptor heterodimers
”NIH-funded study suggests need to boost CD8+ T cell response after infection.”:
Mitochondrial dysfunction, viral persistence and deficient phagocytosis
With "exhausted" CD8+ T cells, it is worth remembering that immune cells also have mitochondria, and they need energy to do their job:
SARS-CoV-2 fragments may cause problems after infection:
Correction of Deficient Phagocytosis During Erythropoietin Treatment in Maintenance Hemodialysis Patients:
" Efferocytosis of apoptotic cells by macrophages which is central in inflammation resolution was impaired in obese mice and restored by exogenous EPO. " : The deficiency of macrophage erythropoietin signaling contributes to delayed acute inflammation resolution in diet-induced obese mice https://lnkd.in/dVEwBNFH
Phagocyte respiratory burst activates macrophage erythropoietin signalling to promote acute inflammation resolution https://lnkd.in/dM2Ucq68
Erythropoietin enhances Kupffer cell number and activity in the challenged liver:
Gut microbiota dysbiosis
Iron dysregulation
Iron dysregulation and inflammatory stress erythropoiesis associates with long-term outcome of COVID-19:
Fatal COVID-19 pulmonary disease involves ferroptosis:
Dysautonomia and POTS
The causes of these conditions are not fully known/understood/agreed upon. But many very likely explanatory factors have been mentioned in the above.
Blood volume perturbations in the postural tachycardia syndrome :
Erythropoietin in Autonomic Failure:
"These patients also have a significant reduction in plasma erythropoietin":
Sexual and reproductive function
Men
Endothelial Dysfunction in Erectile Dysfunction:
In male patients sexual desire, frequency of sexual intercourse was strengthened after rhEPO therapy:
Women
Improvement of sexual function was remarkable in female patients:
Why women more often suffer from LongCovid ?
Adult females mount stronger innate and adaptive immune responses than males: https://www.nature.com/articles/nri.2016.90
This means a stronger EPO-TNFalpha imbalance.
Estrogen suppresses and testosterone increases the production of EPO in the kidneys:
This makes a threshold for younger to middle age female patients to recover their own EPO-production, while in particular younger men quickly recover from or don't get Covid-19 and rarely suffer from LongCovid.
Insights into early recovery from Long COVID—results from the German DigiHero Cohort:
This may thus also explain the age-distribution in LongCovid.
Racial/ethnic differences
Conclusion
EPO deficiency is "the common denominator" in both LongCovid and in Covid-19.
Pathogenesis : the immune response to the virus is so strong (with inflammatory cytokines), that it damages the kidneys EPO production.
Covid-19 and LongCovid are immunologic, hematologic, metabolic, neurologic and endocrinologic diseases.
That sounds complicated, but it is all due to deficiency of a single substance, that stands ready in our common medicine cabinet.
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I found this article, that I also have added above, as I think it is highly relevant.
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I am working on my graduate thesis at Loma Linda University, School of Public Health. The main aim of my study is to explore how aerobic exercise helps improve social, physical, and psychological well-being of patients' caregivers. Numerous studies on the importance of exercise for dementia exist, but research has done very little to showcase the importance of the same approach to catering for caregiver health needs.
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Hello, Linda. I am currently working on research on the impact of caregiving on family caregivers and the tests I am using are the following, taken from the study by Crespo and López (2007) that I reference at the end. This is the adapted table, in case any of them are useful for you:
Contextual variables:
Sociodemographic characteristics (patient and caregiver).
Dependent person's problems: Memory and Behavior Problems Checklist, MBPC (Zarit and Zarit, 1983)
Cognitive impairment: Global Deterioration Scale (GDS) (Reisberg et al., 1982).
Functional impairment: Barthel index
Mediating variables:
Subjective burden: Caregiver Burden Interview (CBI) (Zarit et al., 1980).
Positive aspects of caregiving: Caregiving Satisfaction Scale (Lawton et al., 1989).
Self-esteem: Self-esteem scale (Rosenberg, 1965)
Social support (availability and satisfaction): Social Support Questionnaire, Short Form-Revised (SSQSR) (Saranson et al., 1987).
Caregiving coping strategies: Brief-COPE Inventory (Carver, 1997).
Dependent variables:
Anxiety: Anxiety subscale of the Hospital Anxiety and Depression Scale (HADS) (Zigmond and Snaith, 1983)
Depression: Beck Depression Inventory (BDI) (Beck et al., 1979)
Physical health: GHQ-28 Physical Scale (General Health Questionnaire-28) (Goldberg, 1981)
Health Questionnaire SF-12, 12-Item short-form health survey (Ware, Kosinski and Keller, 1996).
I hope you find it useful :)
Crespo, M., y López, J. (2007). El apoyo a los cuidadores de familiares mayores dependientes en el hogar: desarrollo del programa “Cómo mantener su bienestar”. Madrid: Imserso.
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My research will be exploring the meaning and experiences of career to women living with young onset dementia. Career is conceptualised as life roles, so not necessarily paid employment. I have been exploring Stakian case study as a methodology and am quite keen to use it, taking a multicase instrumental approach (young onset dementia as the research focus). I propose interviewing the participants (women living with dementia) and using an artefact/ creative activity to gain further perspective and as an alternative to document analysis. I am struggling with how I can include a third data collection method to achieve triangulation and avoid ethical difficulties. Initially I was thinking to interview a 'significant other' to the participant's career but this raises issues of confidentiality and discomfort that have led me to conclude I need a new idea, or change my methodological approach. I would welcome any expert opinions to help this decision process! Thank you.
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Triangulation does not necessarily include three methods. The name refers to an analogy with navigation, where two observations are drawn in a way that generates the intersection of lines at the point of a triangle. So, you only need two different data sources for your comparison, but note that they should be as distinct ("independent") as possible.
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Independant variables:
Year: 17/18; 21/22
Age group: Over 65; Under 65
I could turn these into one independent variable: 17/18 over; 17/18 under; 21/22 over; 21/22 under (4 levels)
Dependant variable:
Outcome (3 levels): Dementia; MCI; No diagnosis
Looking at my descriptive statistics, the under 65 group had increased dementia and MCI diagnosis and a decrease in no diagnosis between year 17/18 and 21/22.
Looking at the over 65 group, there were increases in MCI diagnosis, but decreases in Dementia and No Dementia diagnoses between 17/18 and 21/22
I want to see if these changes over time are significant/ looking at effect sizes. But I'm not sure how to do it beyond doing 12 X Chi squared tests which would not be appropriate!
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Thank you all for your input! I first tried a loglinear analysis, but one of my variables did not meet the assumptions and then I got stumped with the interpretation!
Sal Mangiafico, I then used two 2 - way contingency tables! This was much easier, thank you!
Daniil ( Даниил ) Александрович Fedorov ( Федоров ) I do have the ages of the patients. I am just making a comparison between older and younger adults with dementia in this way, as individuals diagnosed under 65 are diagnosed as having young onset dementia. Which is the main reason for my project :-)
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Paratonia is one of the symptoms that are present by people with dementia. All in the beginning re the signs that this has influence on walking/balance but also the selectivity of the hands.(Bieke van Deun , Hans Hobbelen).
But we know that this can develop to an extreme form and create an extreme attitude but how we could handle this tone increase and is our handling also an reason for increase of the tone?
The brain damage is one part but transfers etc. in which the person must counter par example when someone pull him uprigth will this increase the paratonia ???
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dank Thanos
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I am carrying out a study to explore the role of the environment of a long-term care home on older persons living with dementia. The participants of the study will be will be relatives of older persons living with dementia. I will carry out interviews to explore their perspectives and thematic analysis for data analysis.
I need help identifying the worldview/paradigm + ontological/epistemological approach that I will be adopting. How can I identify the theoretical framework that I will be adopting?
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Any citation, current one, to check how I could separate the age groups to yound adults, middle-age adults and older adults?
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Golgi Cenci Foundation [see director Antonio Guaita in ResearchGate, and www.golgicenci.it for results and methodology] focussed on 70 to 74 years old people to follow longitudinally a cohort, since a turnpoint age; we are running the 5th wave
regards, Mauro Colombo
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I'm doing a project to detect signs of Alzheimer's related macular degeneration, for which I would require a dataset of healthy and AD retinal images (ideally also in different stages of the disease), any suggestions of pre-existing datasets or how I might go about cobbling one together? Size and quality of the dataset aren't super high priority as it's a small POC.
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Hi did you find the dataset of retinal imaging for the detection of Alzheimer's?
Could you help me to find some database for this subject to?
Thank you in advance
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I would like to ask one crucial question.
When I monitor Amyloid Beta (AB-42) concentration in cerebrospinal fluid (CSF), I get some values in lower and higher concentraitons. AB-42 concentration range in CSF varies between 200 - 1000 pg/mL according to the literature.
My question is following.
Do higher concentrations or lower concentrations of AB-42 in CSF indicate dementia ?
Thank you all for your answers or comments.
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Lower concentrations of amyloid beta 42 are associated with dementia
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I am planning to conduct an interventional research on nurse's knowledge on dementia which includes pre test, post test and educational intervention.
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It depends on research design, questions, hypotheses, methodology.etc
A selected focus group of say 5 to 10 nurses, with experience of dementia, could provide sufficient initial data. Alternatively/additionally, a small representative sample could be randomly chosen from the nurse population. Quantitative and qualitative approaches could be integrated.
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Mixed dementia is common in the elderly, how useful are these perfusion technqiues in unselected populations with cognitive problems?
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There is a lot of heterogeneity, I think - wide differences from one institution to another. In Australia, for example, it is available at only a few centres so this is rarely done, only referred by relatively select clinicians (eg a few geriatricians).
I would not be surprised if there are very few cases in some countries and more in others.
That, then, leads to the question if only a certain few can afford it (obviously in some countries you can only get it if you pay for it) then does that mean a lot of people who need this cannot get it?
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Dear Colleagues, please fill thiscquestionnaire, it takes only 5 minutes. It os anonymous. For health professionels e.g. nurses and medical doctors. All specialties. Thank you. In advanced for ypur collaboration. Deatails in the first page. Of the link.
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Done
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My friend is looking for coauthors in Psychology & Cognitive Neuroscience field. Basically you will be responsible for paraphrazing, creating figures, and collecting references for a variety of publications. Please leave your email address if you are interested. 10 hours a week is required as there is a lot of projects to be done!
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Paraphrasing and collecting reference, editing work in other word, cannot result in coautorship ! The authors of papers must have been involved in the creative process of the paper, no ? To be honest, I do not think that this kind of request is deontological or even ethical.
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Hello everyone,
My research will interview people living with dementia outside of NHS settings. In the University ethics application I outlined the use of a consultee to ensure people living with dementia who lack capacity have the opportunity to participate. However, what the NHS HRA defines as ‘intrusive research’ involving adults lacking mental capacity cannot be approved under the University's ethics processes, as University ethics committees are not recognised as Appropriate Bodies under the Mental Capacity Act . This is regardless of whether the research is taking place within or outside of the NHS.
The only option I can see to avoid HRA application, is not including people who lack capacity to consent. I do not want to take this route as it seems inequitable. This doesn't sit well with me and I wonder if anyone has confronted this issue in the past?
Any advice and information welcomed!
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In order for adults lacking capacity to participate in non-clinical trial research it must be connected with an impairing condition in the functioning of the mind or brain affecting the person (or its treatment), which causes or contributes to the impairment. a person must be assumed to have capacity unless established otherwise. Individuals should be helped to make their own decisions as far as practicable. A person is not to be treated as unable to make a decision merely because he makes an unwise decision. All decisions and actions must be in the best interests of the person lacking capacity. All decisions and actions must be the least restrictive of the person’s rights and freedom of action. Capacity refers to the everyday ability that individuals possess to make decisions or to take actions that affect them, from simple decisions such as what to have for breakfast to far-reaching decisions about serious medical treatment or financial affairs.
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If there is Immunological Memory, there is also possibility of;
Immunological Dyslexia.
Immunological Dementia.
Immunological Amnesia.
Is it not ?
And such effects might occur as a result of adaptations in epigenetic system of individuals accompanied by ageing, co-morbidities, polypharmacy etc ?
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All over the world, rates of dementia are expected to rise dramatically over the coming decades. And research continues to suggest that actions that have been taken early can reduce the risk of this disease. There are about 10 million new cases, each year, of dementia, which is a general term for groups of symptoms associated with deterioration of the brain. We know that what we eat can affect our physical health. But it could affect the brain too.
So, it is possible that there is a link between our diet and the risk of the development of dementia? Is there any effective food that can reduce the risk of the development of this disease? How can we reduce the risk of dementia through diet?
All comments and contributions are welcome.
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Thanks a lot, Dr. Martin Hofmeister Yes, a number of studies are pooled on the benefits of sticking to a Mediterranean-style diet to stave off brain decline. Most of the studies focused on the overall benefits of the diet, but one study delved into the specific ingredients that help. Harvard Health cited a study by researchers at the National Institutes of Health that evaluated the lifestyles of more than 7,750 participants and followed them for five to 10 years. They used this data to identify the dietary factors that were most important in reducing the risk of cognitive impairment, as well as the dietary factors that were most important in reducing the risk of cognitive decline. Harvard Health reported that fish was the “most important dietary factor” in reducing the risk of cognitive impairment. https://middleeast.in-24.com/News/162859.html
We are so grateful for sharing these valuable and informative links about this thread...My sincere gratitude, Doctor.
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Research publications and datasets for diagnosis of dementia patients.
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Hello Mr Pise.
I hope you’re doing good. I’m currently working on validating observer-rated only scales to assess presence of depressive symptoms in moderately severe dementia (in the nursing field).
Throughout hundreds of articles I’ve read, I saw a lack of consensus on how to diagnose depression in dementia (e.g.: ICD-10 criteria, DSM, PDC-dAD, etc.). For the Alzheimer’s type dementia, some studies suggest the use of the Provisional Diagnostic Criteria for Depression of Alzheimer's Disease (PDC-dAD). A lot of studies use this criteria measure (PDC-dAD) as the reference standard for depression diagnosis in other types of dementia (ex: vascular, fronto-temporal, ect.), however the same limit always come back to surface: the PDC-dAD was developed for Alzheimer’s disease and never validated for any other types of dementia. This being said, there seems to be a need in developing a consensus for depression diagnosis in diverse dementia types/severity. It would be very interesting to either validate the PDC-dAD in different dementia types/severity or construct a new universal criteria measure for depression in all dementia types (or one who incorporates criteria for the different types). All studies I’ve seen on the assessment of depression in dementia discusses how the main difficulty for healthcare providers (physicians and nurses) is the bidirectional relationship between the two problems and how symptoms of depression in this clientele could actually be behavioral and psychological symptoms of dementia or vice versa, leading to over or under detection/diagnosis of depression.
I hope my answer is the type you are looking for and hope this helps! Have a nice day!
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Dear Sirs and Madams, Doctors and Nurses
please fill this anonymous questionnaire about Dementia and palliative care. You needonly 5 minutes. Thank you to help this research study.
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Done
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We would like to start using a program to build pedigrees for our genetic CJD and dementia cohorts. The program should allow to incorporate and search for clinical data.
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FamGenix is a family health history platform that allows you to build pedigrees yourself or auto-generate them by gathering family history data from patients/family members via the app/web portal. It also includes custom surveys that can be sent to participants. On the provider portal you can enter/search clinical data and review/edit pedigrees. https://famgenix.com
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Does anyone have "good" Journal suggestions for publications in China or India? Topic related to dementia or neurodegeneration. (searches give thousands and it is difficult to know).
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Chinese Medical Journal may be a good choice. It is an authoritative medical journal with a long history in China, and its status is similar to that of BMJ.
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Dear Colleagues
We kindly ask you to fulfill this anonymous questionnaire about knowledge and attitudes for the care of people with advanced dementias (severe neurocogntive disorders in DMS-V terminology). Thanks in advance to contribute to the research progresses in this important field.
The questionnaire is for Nurses and Medical doctors.
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👌🏾
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Hello.
I am looking for research/papers about using food to decrease behavioral and psychological symptoms in dementia (BPSD). The focus is on behavioral disturbances such as eg. wandering, aggression and insomnia. I am interested of effects of both food deprivation and/or postprandial somnolence but even other suggestions and inputs are welcomed.
Sending my best regards - Sabina Dalsborn
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Do you have any links to suggest?
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I am working on the effect of music therapy on persons with Alzheimer's Disease. I require EEG signals of healthy individuals and people with Alzheimer's Disease/Dementia that have undergone music therapy. Due to the on-going pandemic, I am unable to collect signals in real-time. It would be helpful if I could be directed to a database that I can get EEG signals from.
Thank You.
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I have enclosed a music therapy and Alzheimer's review of literature article for your perusal. Chris
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Omega 3 fatty acids have a different wide beneficial effect on many tissues. Does it show any protection against dementia?  
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Also, see the following RG link.
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Professionals should carry out their tasks and assignments without bringing too much of emotion into it. Diagnoses should be taken into account, rather than trying to make it a routine, instead of patient-oriented.
An example of three patients suffering from different, but quite symptomatically similar dementia that are sometimes termed or tagged "aggressive". Aggression, breeds counter aggression. There I see this said aggressive nature as a special method of communication.
It could be that the attitudes of the professionals in question, seem to, either be untrusted, not understood, strange and even unfriendly in nature. So because one staff may have documented a patient to be aggressive, makes and put such patient on a "red" list. Thereby making it look like preparing for a battle when preparing to attend to such patient.
It is but quite interesting to know that, these patients react very differently to some other staff - a very calm and friendly manner. The act of caring seen as an art, science, even as a particular technique. It should not be taken or perceived as a one way route, but rather individualised, in essence, patient-centred-care.
The biography of patients should not be underestimated, but put to use as a tool or road map to achieving a goal. By doing this, it make caring, nursing and therapy, as the case may be, interesting, rather than otherwise.
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Good question Muhammad Aledeh for this interesting topic.
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Hi everyone. I am working on HT22 cell line in-vitro experiment to study dememtia.
I have mostly seen that they usually induce this cell death with H2O2 or glutamate.
BUT why very few people use SCOPOLAMINE?
Because in mouse or rat model, people usually use SCOPOLAMINE to make a dementia model.
Take this paper for example:
Animal experiment: use scopolamine indced modle.
Cell experiment: use glutamate and H2O2.
(Why didn't the author use scopolamine-induced HT22 cell death?)
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you need to ask ourself, first, what are you going to study. Are you studying cell death per se? Do you want to study dementia, and if so, is this the right model and is cell death the most important factor to be studied? Cell lines are great to study biochemistry, sort of great for cell biology, much less great to study neuroscience, even less great to study neurodegeneration.
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I am currently working with predict dementia with a machine learning project. Mainly I am focusing to develop a mobile-based application that consists series of questions designed to test a range of everyday mental skills.
This mobile-based application depends on effective feature attributes that impact the diagnosis of dementia from the already diagnosed clinical patients.
With this covid-19 situation, I have found it difficult to find a dataset for my project. Can anyone suggest/ideas about publicly available datasets for my project ?
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Applying Deep Learning to Predicting Dementia and Mild Cognitive Impairment
Guest Editor (s): Ilias Maglogiannis, Lazaros Iliadis, and Elias Pimenidis
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I have been doing immunohistochemistry of Beta Amyloid on adult healthy cynomolgus monkey brains with the 4G8 and 6E10 antibodies, which were from the Covance company. I found there was 4G8 immunostained intracellular Aβ in a granular pattern in the monkey brains. However, no reaction stained with 6E10 antibody was found. I checked the datesheet of these two antibodies and found that the 6E10 is reactive to amino acid residue 1-16 of beta amyloid while the 4G8 recognizes amino acid residues 17-24 of beta amyloid. I am confused about the result. Consequently, I wonder if there were some differences of structure/function or processing of APP between Aβ1-16 and Aβ17-24.
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This paper might help you out:
Hunter and Brayne Journal of Negative Results in BioMedicine (2017) 16:1 DOI 10.1186/s12952-017-0066-3
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Hi,
I am interested to carry out a thesis on early prediction of Dementia using csv/excel type data. Can someone please assist?
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Regarding variable will you use in your thesis, I have some suggestions for you:
1. For y (dependent) variable, that is dementia, type of the variable is binary (i.e. 1 and 0,where 1 represents dementia and 0 is not dementia)
2. For x (independent) variable, you have to specify it before hand. I mean you have to ensure these variables affect and can be used to predict dementia. Do Exploratory data analysis before doing prediction.
Have you done with all of these?
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I found the Cohen-Mansfield scale, but it is for weekly use. I'm looking for the same type of rating scale or grid that can be used evey day by home caregivers, so it has to be easy to fill. Thank you for your help!
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Rating Scale for Aggressive Behaviour in the Elderly (RAGE)
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Hola
I'm working on a project that deals with clinical named entity recognition, relation extraction etc. I'm currently using Scispacy library for NER work. However, I'm searching for a open source package for relation extraction from clinical notes (Eg. In the following sentence "Dementia due to Alzheimer disease." I except a model that should recognize the relationship that its not just dementia and its is dementia due to Alzheimer.)
Spending sometime on reading articles and surfing google
I found the following packages:
1. SemRep
2. BioBERT
3. Clincal BioBERT
etc.
from the articles, I also got to know that clincal BioBERT to be the suitable model. However, when I tried running the model from transformer library I just found the following output
Code
from transformers import AutoModelForTokenClassification, AutoTokenizer, pipeline
model =  AutoModelForTokenClassification.from_pretrained("emilyalsentzer/Bio_Discharge_Summary_BERT")
tokenizer = AutoTokenizer.from_pretrained("emilyalsentzer/Bio_Discharge_Summary_BERT")
nlp = pipeline('ner', model=model, tokenizer=tokenizer)
text = "Dementia due to Alzheimers disease. Kidney failure due to liver disease."
nlp(text)
Out put:
[{'entity': 'LABEL_1', 'index': 1, 'score': 0.562394917011261, 'word': 'dementia'}, {'entity': 'LABEL_0', 'index': 2, 'score': 0.5325632691383362, 'word': 'due'}, {'entity': 'LABEL_1', 'index': 3, 'score': 0.5473843812942505, 'word': 'to'}, {'entity': 'LABEL_1', 'index': 4, 'score': 0.5070908069610596, 'word': 'alzheimer'}, {'entity': 'LABEL_0', 'index': 5, 'score': 0.5742462873458862, 'word': '##s'}, {'entity': 'LABEL_1', 'index': 6, 'score': 0.5498184561729431, 'word': 'disease'}, {'entity': 'LABEL_1', 'index': 7, 'score': 0.5163406133651733, 'word': '.'}, {'entity': 'LABEL_1', 'index': 8, 'score': 0.5038259625434875, 'word': 'kidney'}, {'entity': 'LABEL_1', 'index': 9, 'score': 0.5872519612312317, 'word': 'failure'}, {'entity': 'LABEL_0', 'index': 10, 'score': 0.523786723613739, 'word': 'due'}, {'entity': 'LABEL_1', 'index': 11, 'score': 0.5193214416503906, 'word': 'to'}, {'entity': 'LABEL_1', 'index': 12, 'score': 0.5457456707954407, 'word': 'liver'}, {'entity': 'LABEL_1', 'index': 13, 'score': 0.5755748748779297, 'word': 'disease'}, {'entity': 'LABEL_1', 'index': 14, 'score': 0.5418881177902222, 'word': '.'}]
From the above output, I except labels such as disease, organ etc. However, the model labeled the entity as 'LABEL_1' or 'LABEL_0'.
How do I use the clinical BioBERT to extract relations. Please advice.
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Hi all
I'm starting to research rating scales to assess symptoms of agitation or anxiety in patients with dementia. If you know any papers or resources Id be very grateful for suggestions
Kind regards
P.J.
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Many thanks for this. This is really useful!
P.J.
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Hi All, I am looking at compiling a wide list of papers or resources on reminiscence therapy for dementia for older people. The positive and negative results, Creative approaches, ICT interventions, standard procedures, etc. I'm interested in perspectives from differing disciplines. All resources/ papers/ leads welcome Thank you!
P.J.
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It feels great to share it. Hope you find it useful P.J. White
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The link between type 2 diabetes and dementia: from biomarkers to treatment
  • Michal Schnaider Beeri
  • Barbara B Bendlin
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I am looking to apply supervised machine analytics on a dataset that shows the location-based movement of patients in a house. The database needs to show the indoor movements of patients. The dataset may have both numerical or categorical values.
An example of this is the demonstration of the time the person woke up, any chores/activities the patient did, the time the patient went to sleep, etc. I would prefer the dataset to be labeled defining the abnormal and normal occasions.
Ideally, I will be applying supervised machine learning algorithms to the patient's movements. For future work unsupervised machine learning analytics can be applied.
Should you know of any of the specific types of datasets, please let me know.
Thanks
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Hi Donna, thanks for this. However, I have been looking for the data collected from these types of sensors. There are usually motion detection sensors applied to patients' houses to collect information based on when there is motion detected in each room.
This type of data is usually found on Kaggle or UCI machine learning websites, but there is not anything similar available.
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I have just registered on PROSPERO the protocol for a systematic literature review and started wondering to witch journals could I submit it. The review is on the use of therapeutic music-based interventions, in the acute hospital setting, with patients with dementia.
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Dear Dr.Lidia,
There are many online journals, such as American Journal of Infectious Diseases and Microbiology, American Journal of Public Health Research, Biomedical Research International, Journal of One Health etc, in which review articles can be published.I have published reviews in all these journals.
Stay safe and healthy.
With kind regards,
Prof.Dr.Mahendra Pal
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Lancet followed by JAMA and others published today announced "new" recommendations to help prevent '40%' of dementia. The thing is, none of this is new. It is all what I learned as 'common sense' sixty years ago, as a child. From the title I was expecting some earth-shattering new discovery, but no it was the same old doctrine. After trying all of these recommendations for the past 60 years, I can tell you that in average lifetime, many are not obtainable even with vigorous effort based upon knowledge. I would also say that this 40% reduction is already built into society, and the 40% just cannot or will not follow the guidelines. Also, some of the risk factors are built into the aging process, diabetes, hypertension, decreased mobility, chance of head trauma, etc. Although not stated, this "new" set of guidelines may be promoting the greater use of medicinal control. The authors, I don't believe, laid any blame on genetics, which I think is also important. I, as an example, have risk factors, despite trying to control them for 60 plus years, and don't have dementia that i am aware of, but also have none in my family who commonly live over a century. Genetics, family history, is also important I believe. There is also no mention of limiting exposure to neurotoxins, which (as a Medical Toxicologist) I think is a major contributor to dementia. This also foregoes the effect of viruses on neural function, including the possible effects of the novel coronavirus and others on dementia. Now, identifying these additional factors may have been "new" and revolutionary. Thank you and stay safe. Gary Ordog, MD September 24, 2020.
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We encourage all patients, especially those with early dementia and those with risk factors for dementia, to maintain or increase physical activity and exercise as long as there are no contraindications.
●Mediterranean-style diets that are high in fruits, vegetables, whole grains, beans, nuts, and seeds and include olive oil as an important source of fat have been associated with a variety of health benefits, including reduced cardiovascular risk, which may directly or indirectly reduce dementia risk.
●Prospective studies and randomized controlled trials have not shown an overall benefit from vitamins, statins, cholinesterase inhibitors, estrogen replacement, or nonsteroidal antiinflammatory drugs (NSAIDs) for the prevention of dementia.
●While vitamin E is not recommended in healthy adults for the purposes of preventing dementia,
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People with Dementia (PwD) have difficulty living their daily lives. And to help PwD, the caregiver is one of several solutions. However, caregivers also have many challenges in helping PwD. Because the memory and thinking decreased dramatically, PwD usually has many symptoms such as Agitation and Anxiety, repetitive questions, depression, hallucinations, sleep disturbances, etc. which make PwD refuse to be helped by caregivers. Therefore, approaches or methods that can help caregivers are needed so that their efforts to support PwD are successful. I have read "humanitude" which is one of the most successful methods. But are there other methods you might know about? Please share. Thank you.
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See: Johnson, C and Johnson, R. (2000) Alzheimer's disease as a trip back in time. American Journal of Alzheimer's Disease April or the short British Alzheimer's Society one page article. for an explanation of the time Travel model of AD. The updated version with more positive language in in the 2017 Behavioral Science journal article.
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Substance-P is an example of peptide neurotransmitter present in hippocampus, neocortex region of brain which involved in perception of pain. I want to know is any link between this neurotransmitter to Alzheimer's or other type of dementia?
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There most likely are many causes of AD.
One prominent theory is loss of autophagy. This dysfunction
allows deposition of tau protein. Rapamycin inhibition of the
mTOR pathway allows improvement in autophagy and repair
of damaged proteins etc.and suggests therapeutic effects.
Mitochondrial dysfunction is also involved. The loss of normal
cell function due to severe mitochondrial damage from various insults
ie ischemia, toxins, hyperglycemia, direct physical damage etc.
Cells die at an advance rate via apoptosis.
I love this topic....so much to learn
Lester Mandelker DVM
Fellow AAVPT
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The Novel Object Recognition Test (NORT) is now among the most commonly used behavioral tests for rodents, It is used to evaluate cognition, particularly recognition memory in rodent models of CNS disorders (Ennaceur and delacour, 1988), relies on the innate preference and the natural tendency of rodents to spend more time exploring novel objects than familiar ones (Cohen and Stackman, 2015).
Our studies are about testing the enhancer potential of phytochemicals on memory impairment in Aged rats, and other models of impair cognition (e.g NMDA antagonists (MK-801) and muscarinic antagonists (scopolamine), for the purpose we would be so grateful
I would like to know :
How many times can we use this test during a treatment period of 14 days ? And will there be any effect of this repetition on the effectiveness and the results of this test?
Thank you in advance.
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Our study is based on two behavioral tests the Y-Maze test, which in it the spatial working memory was evaluated based on the percentage of correct alteration between the three arms (A, B and C), and the NOR test to analyze the nonspatial working memory in Scopolamine-induced memory impairment model. And other biochemical parameters such as dosing antioxidants enzymes, lipid peroxidation in both brain and serum ....
Is that enough !!! To confirm the anti-amnesic potential of a plant ?
Ansab Akhtar Thanks Sir for your valuable help. 🌹
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Dear colleagues and other scholars,
I'm a psychiatry resident currently working on a review about BPSD management. However, one thing I haven't understood is: "Why is it that researcher and clinicians group BPSD as if it was a single entity?"
Given the varied symptoms of BPSD, is it logical to group it as a single syndrome just because it's happening along with dementia? Or does it have a well-established psychopathology to justify the grouping?
Does anyone have a good reference regarding this issue?
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I just saw your question from quite a while ago, so I'm not sure if it's still relevant but others might find the information useful as well...
There is good evidence the BPSDs co-occur. In the paper attached, we showed a high degree of BPSD comorbidity in a representative sample of PwD living in residential care (in Australia).
While all BPSDs do not occur in all forms of dementia, some form of BPSD is common in most forms of dementia. BPSD are grouped together because they are associated with damage to the brain (and deficits associated with this) and they can often be treated in similar ways, which often differ from the way the condition would be treated in a person without dementia.
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The Greater Cincinnati Well-being Observation Tool developed by Clarissa Rentz (2005).