Article
Ceruloplasmin induces polymorphonuclear leukocyte priming in localized aggressive periodontitis.
Department of Periodontology and Oral Biology, Boston University Goldman School of Dental Medicine, Boston, MA, USA.
Journal of Periodontology (impact factor:
2.6).
08/2009;
80(8):1300-6.
DOI:10.1902/jop.2009.090092
pp.1300-6
Source: PubMed
- Citations (2)
-
Cited In (0)
-
Article: Resistance to thyroid hormone caused by a new mutation (V336M) in the thyroid hormone receptor beta gene.
[show abstract] [hide abstract]
ABSTRACT: Resistance to thyroid hormone (RTH), usually caused by an inherited defect of the thyroid hormone receptor, (TRbeta), results in a reduced responsiveness of target tissues to thyroid hormone. Until now, more than 600 cases with RTH have been identified. Although usually linked to the TRbeta gene, located on chromosome 3, RTH may also occur in the absence of mutations in the coding region of this gene. We report a 10-month-old boy who had laboratory findings typical of RTH. He was born prematurely on the 34th week of gestation and his thyrotropin (TSH) during neonatal screening was 121 microU/mL, a value very high for RTH or prematurity. Direct sequencing of the TRbeta gene from the patient's genomic DNA revealed a heterozygous substitution of the normal valine with a mutant methionine in codon 336 (V336M) that has not been previously reported. In vitro expression studies showed that this mutant TRbeta has an impaired triiodothyronine (T3)-dependent transactivation that reduces the activity of the wild-type TRbeta (dominant negative effect). While the functional impairment of V336M is not unusual compared to other TRbeta gene mutations, the very high TSH value in this prematurely born infant suggests that fetuses with RTH have altered maturation of the hypothalamo-pituitary-thyroid axis or actually may suffer from hypothyroidism.Thyroid 11/1999; 9(10):1001-4. · 4.79 Impact Factor -
Article: Serum caeruloplasmin as a coronary risk factor in the elderly: the Rotterdam Study.
[show abstract] [hide abstract]
ABSTRACT: Serum Cu and caeruloplasmin levels have been suggested to be independent risk factors for CHD operating through oxidative modification of LDL. However, given its function as an acute-phase protein, the question has been raised whether an elevated caeruloplasmin level is not merely an indicator of inflammation. In the current study, we investigated whether serum caeruloplasmin was associated with subsequent myocardial infarction, taking into account indices of inflammation. The study population consisted of 210 cases of first myocardial infarction and controls, frequency-matched on age (5-year categories) and sex, selected from the population-based cohort of the Rotterdam Study. Serum caeruloplasmin levels were significantly elevated in cases of myocardial infarction compared with controls (510 (SD 110) v. 470 (SD 100) mg/l; P = 0.007). Risk of myocardial infarction for the highest compared with the lowest quartile of caeruloplasmin was 2.46 (95% CI 1.04, 6.00; Ptrend = 0.043) after adjustment for age, sex, BMI, pack-years smoked, serum cholesterol, systolic blood pressure, and income. The relative risk was most evident in current smokers. Adjustment for C-reactive protein and leucocyte count reduced the excess risk by 33%. This suggests that a substantial part of the observed association between serum caeruloplasmin and CHD may be attributed to inflammation processes rather than to the pro-oxidant activity of caeruloplasmin.British Journal Of Nutrition 03/1999; 81(2):139-44. · 3.01 Impact Factor
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed.
The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual
current impact factor.
Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence
agreement may be applicable.
Keywords
CP levels
cytochrome-C reduction
enzyme-linked immunosorbent assay
Exogenous CP treatment
healthy donors
healthy PMNs
healthy subjects
Intracellular CP expression
Intracellular iron ion conversion
iron conversion
iron ion conversion
LAgP PMNs
Local inflammation
localized aggressive periodontitis
PMNs
Polymorphonuclear leukocytes
real-time polymerase chain reaction
serum samples
superoxide
Western blotting