Exonic polymorphism (rs315952, Ser133Ser) of interleukin 1 receptor antagonist (IL1RN) is related to overweigh/obese with hypertension
Recent studies demonstrated that interleukin 1 receptor antagonist (IL-1RN) plays an important role in metabolic effects. To investigate wheth-er IL1RN polymorphisms are associated with obesity, two single nucle-otide polymorphisms (SNPs) of the IL1RN gene [rs4251961 (-828, T>C) and rs315952 (Ser...
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Published in | Journal of exercise rehabilitation Vol. 10; no. 5; pp. 332 - 336 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Society of Exercise Rehabilitation
01.10.2014
한국운동재활학회 |
Subjects | |
Online Access | Get full text |
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Summary: | Recent studies demonstrated that interleukin 1 receptor antagonist (IL-1RN) plays an important role in metabolic effects. To investigate wheth-er IL1RN polymorphisms are associated with obesity, two single nucle-otide polymorphisms (SNPs) of the IL1RN gene [rs4251961 (-828, T>C) and rs315952 (Ser133Ser)] were analyzed in 122 overweigh/obese and 123 control subjects. Overweigh/obese subjects were classified ac-cording to body mass index (BMI). SNPStats was used to obtain odds ratios (ORs), 95% confidence intervals (CIs), and P values. Multiple lo-gistic regression models (codominant1, codominant2, dominant, reces-sive, and log-additive) were conducted to analyze the genetic data. Synonymous SNP (rs315952) of the IL1RN gene was associated with overweigh/obese with hypertension (OR=4.98, 95% CI=1.74-14.19, P=0.003 in codominant 1 model and OR=3.98, 95% CI=1.48-10.74, P=0.0029 in dominant model). However, another SNP (rs4151961) did not show association with overweigh/obese or overweigh/obese with hypertension. These results suggest that exonic SNP of IL1RN (rs 315952, Ser133Ser) may be contributed to overweigh/obese with hyper-tension. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 G704-SER000008925.2014.10.5.015 |
ISSN: | 2288-176X 2288-1778 |
DOI: | 10.12965/jer.140155 |