Wu Jingjing, Liu Zheng, Meng Kai, Zhang Ling
Department of Epidemiology and Biostatistics, School of Public Health, Capital Medical University, Beijing, China; Beijing Municipal Key Laboratory of Clinical Epidemiology, Beijing, China.
Department of Hospital Management, School of Health Administration and Education, Capital Medical University, Beijing, China.
PLoS One. 2014 Apr 16;9(4):e95270. doi: 10.1371/journal.pone.0095270. eCollection 2014.
Adiponectin plays an important role in regulating glucose levels and fatty acid oxidation. Multiple studies have assessed the association between rs2241766 polymorphism in the adiponectin (ADIPOQ) gene and obesity susceptibility. However, the results are inconsistent and inconclusive. The aim of this meta-analysis was to investigate this association in adults.
Several electronic databases were searched for relevant literature published up to November 2013. Statistical analyses were performed using software Review Manager (Version 5.02) and STATA (Version 10.0). The pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated with a random-effects model or a fixed-effect model depending on heterogeneity among studies. Q tests and Egger's tests were performed to assess heterogeneity and publication bias. Sensitivity analysis was conducted to confirm the reliability and stability of the meta-analysis.
A total of 2,819 obese and 3,024 controls in 18 case-control studies were included in the meta-analysis. The results indicated that compared with TT genotype, the ADIPOQ-rs2241766 GG genotype was associated with an increased risk for obesity (OR = 1.39, 95% CI: 1.11-1.73, P for heterogeneity = 0.520, I2 = 0%) in overall studies. Whereas, GT genotype was associated with a borderland increased risk for obesity (OR = 1.13, 95% CI: 0.94-1.36, P for heterogeneity = 0.006, I2 = 51%). The susceptibility of obesity was increased based on genotypes of TT<GT<GG (P for trend = 0.011). Subgroup analysis of different regions revealed that the ADIPOQ-rs2241766 GG genotype increased obesity risk in the Chinese studies (OR = 1.54, 95% CI: 1.19-2.00) but not in the non-Chinese studies (OR = 1.02, 95% CI: 0.66-1.58). Similar results were observed in allelic, recessive, and dominant genetic models. There was no significant evidence of publication bias in the overall, Chinese, and non-Chinese studies (P = 0.426, P = 0.935, and P = 0.390, respectively).
The results of this meta-analysis suggest that the ADIPOQ-rs2241766 G/T polymorphism might be associated with obesity in Chinese studies but not in non-Chinese studies in adults. Better-designed studies that consider confounding factors and assess larger sample sizes with a focus on ADIPOQ-rs2241766G/T polymorphisms and obesity are required in the future.
脂联素在调节血糖水平和脂肪酸氧化中起重要作用。多项研究评估了脂联素(ADIPOQ)基因中rs2241766多态性与肥胖易感性之间的关联。然而,结果并不一致且尚无定论。本荟萃分析的目的是研究成年人中的这种关联。
检索了多个电子数据库,以查找截至2013年11月发表的相关文献。使用Review Manager软件(5.02版)和STATA软件(10.0版)进行统计分析。根据研究间的异质性,采用随机效应模型或固定效应模型计算合并比值比(OR)和95%置信区间(CI)。进行Q检验和Egger检验以评估异质性和发表偏倚。进行敏感性分析以确认荟萃分析的可靠性和稳定性。
荟萃分析纳入了18项病例对照研究中的2819名肥胖者和3024名对照。结果表明,在总体研究中,与TT基因型相比,ADIPOQ-rs2241766 GG基因型与肥胖风险增加相关(OR = 1.39,95% CI:1.11 - 1.73,异质性P = 0.520,I2 = 0%)。而GT基因型与肥胖风险边缘性增加相关(OR = 1.13,95% CI:0.94 - 1.36,异质性P = 0.006,I2 = 51%)。基于TT<GT<GG基因型,肥胖易感性增加(趋势P = 0.011)。不同地区的亚组分析显示,ADIPOQ-rs2241766 GG基因型在中国研究中增加了肥胖风险(OR = 1.54,95% CI:1.19 - 2.00),但在非中国研究中未增加(OR = 1.02,95% CI:0.66 - 1.58)。在等位基因、隐性和显性遗传模型中观察到类似结果。在总体、中国和非中国研究中均无明显的发表偏倚证据(分别为P = 0.426、P = 0.935和P = 0.390)。
本荟萃分析结果表明,ADIPOQ-rs2241766 G/T多态性在中国成年人研究中可能与肥胖相关,但在非中国成年人研究中并非如此。未来需要设计更完善的研究,考虑混杂因素并评估更大样本量,重点关注ADIPOQ-rs2241766 G/T多态性与肥胖的关系。