Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, 157 Baojian Road, 150086, Nangang District, Harbin, China.
Acta Diabetol. 2013 Apr;50(2):267-72. doi: 10.1007/s00592-010-0247-8. Epub 2010 Dec 29.
Epidemiological studies on the association between the single nucleotide polymorphism (SNP) at -420 C/G (rs1862513) in the human resistin gene (RETN) and the risk of type 2 diabetes mellitus (T2DM) are conflicting. In order to derive a more precise estimation of the association, a meta-analysis was conducted. Twelve studies with 5,935 cases and 5,959 controls were enrolled by searching the databases of Medline, EMBASE, and Cochrane. Summary odds ratios (ORs) with 95% confidence intervals (CIs) were calculated. The heterogeneity and publication bias were investigated. The main analysis indicated no significant association [for allelic model: OR = 0.97 (0.92-1.03); for additive model: OR = 0.95 (0.83-1.09); for recessive model: OR = 0.98 (0.86-1.12); for dominant model: OR = 0.95 (0.88-1.04)]. Overall, no significant heterogeneity was found. Subgroup analysis by race and source of controls indicated no significant association. In conclusion, the current meta-analysis did not observe any association between the polymorphism of RETN -420 C/G and the risk of T2DM. The study may help us further understand the genetics of T2DM. However, larger and prospective studies are warranted to confirm this finding.
关于人类抵抗素基因(RETN)中-420 C/G(rs1862513)单核苷酸多态性(SNP)与 2 型糖尿病(T2DM)风险之间的关联的流行病学研究结果存在争议。为了更准确地评估这种关联,进行了荟萃分析。通过搜索 Medline、EMBASE 和 Cochrane 数据库,共纳入了 12 项研究,包含 5935 例病例和 5959 例对照。计算了汇总优势比(OR)及其 95%置信区间(CI)。对异质性和发表偏倚进行了调查。主要分析表明,没有显著关联[等位基因模型:OR=0.97(0.92-1.03);加性模型:OR=0.95(0.83-1.09);隐性模型:OR=0.98(0.86-1.12);显性模型:OR=0.95(0.88-1.04)]。总体上,没有发现显著的异质性。按种族和对照来源进行的亚组分析也未发现显著关联。综上所述,本荟萃分析未观察到 RETN-420 C/G 多态性与 T2DM 风险之间存在关联。该研究可能有助于我们进一步了解 T2DM 的遗传学。然而,需要更大规模的前瞻性研究来证实这一发现。