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Genetic Polymorphisms in Adipokine Genes and the Risk of Obesity: A Systematic Review and Meta‐Analysis

Polymorphisms in adipokine genes, such as leptin (LEP), leptin receptor (LEPR), resistin (RETN), adiponectin (ADIPOQ), interleukin‐1β (IL‐1β), IL‐6 (IL‐6), and tumor necrosis factor‐α (TNF‐α) may be involved in the development of obesity. We conducted a systematic review of published evidence on the...

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Published in:Obesity (Silver Spring, Md.) Md.), 2012-02, Vol.20 (2), p.396-406
Main Authors: Yu, Zhangbin, Han, Shuping, Cao, Xingguo, Zhu, Chun, Wang, Xuejie, Guo, Xirong
Format: Article
Language:English
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Summary:Polymorphisms in adipokine genes, such as leptin (LEP), leptin receptor (LEPR), resistin (RETN), adiponectin (ADIPOQ), interleukin‐1β (IL‐1β), IL‐6 (IL‐6), and tumor necrosis factor‐α (TNF‐α) may be involved in the development of obesity. We conducted a systematic review of published evidence on the association between different adipokine genes and the risk of obesity. Librarian‐designed searches of PubMed and HuGeNet, review of reference lists from published reviews and content expert advice identified potentially eligible studies. The genotyping information and polymorphisms of different adipokine genes, numbers of genotyped cases and controls and frequencies of genotypes were extracted from 48 eligible studies included in this review. Twenty‐one polymorphisms each associated with obesity in at least one study were identified. Polymorphisms in the adipokine genes, LEP, LEPR, and RETN were not associated with obesity susceptibility, whereas ADIPOQ G276T (T vs. G: odds ratio (OR), 1.59; 95% confidence interval (CI), 1.39–1.81), IL‐1β C3953T (CC vs. CT+TT: OR, 1.61; 95% CI, 1.18–2.20), and TNF‐α G308A (GG vs. GA+AA: OR, 1.19; 95% CI, 1.02–1.39) polymorphisms were associated with an increased risk of obesity. The IL‐6 G174C polymorphism was also associated obesity when using allelic comparisons, the recessive genetic model and the dominant genetic model with OR (95% CI) of 1.95 (1.37–2.77), 1.44 (1.15–1.80), and 1.36 (1.16–1.59), respectively. No significant evidence of publication bias was present. However, these “null” results were underpowered due to a small pooled sample size, and analysis of additional case‐control studies with larger sample sizes should provide further clarifications.
ISSN:1930-7381
1930-739X
DOI:10.1038/oby.2011.148