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脂联素变异的遗传分析及其与非裔美国人 2 型糖尿病的关系。

Genetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans.

机构信息

Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, USA; Center for Genomics and Personalized Medicine Research, Wake Forest School of Medicine, Winston-Salem, NC, USA; Center for Diabetes Research, Wake Forest School of Medicine, Winston-Salem, NC, USA.

出版信息

Obesity (Silver Spring). 2013 Dec;21(12):E721-9. doi: 10.1002/oby.20419. Epub 2013 Jun 11.

Abstract

OBJECTIVE

Adiponectin is an adipocytokine that has been implicated in a variety of metabolic disorders, including T2D and cardiovascular disease. Studies evaluating genetic variants in ADIPOQ have been contradictory when testing association with T2D in different ethnic groups.

DESIGN AND METHODS

In this study, 18 SNPs in ADIPOQ were tested for association with plasma adiponectin levels and diabetes status. SNPs were examined in two independent African-American cohorts (nmax = 1,116) from the Insulin Resistance Atherosclerosis Family Study (IRASFS) and the African American-Diabetes Heart Study (AA-DHS).

RESULTS

Five polymorphisms were nominally associated with plasma adiponectin levels in the meta-analysis (P = 0.035-1.02 × 10(-6) ) including a low frequency arginine to cysteine mutation (R55C) which reduced plasma adiponectin levels to <15% of the mean. Variants were then tested for association with T2D in a meta-analysis of these and the Wake Forest T2D case-control study (n = 3,233 T2D, 2645 non-T2D). Association with T2D was not observed (P ≥ 0.08), suggesting limited influence of ADIPOQ variants on T2D risk.

CONCLUSIONS

Despite identification of variants associated with adiponectin levels, a detailed genetic analysis of ADIPOQ revealed no association with T2D risk. This puts into question the role of adiponectin in T2D pathogenesis: whether low adiponectin levels are truly causal for or rather a consequence.

摘要

目的

脂联素是一种脂肪细胞因子,与多种代谢紊乱有关,包括 2 型糖尿病和心血管疾病。评估 ADIPOQ 基因变异与不同种族 2 型糖尿病相关性的研究结果相互矛盾。

设计和方法

本研究检测了 ADIPOQ 中的 18 个 SNP 与血浆脂联素水平和糖尿病状态的相关性。在来自胰岛素抵抗动脉粥样硬化家族研究(IRASFS)和非裔美国人糖尿病心脏研究(AA-DHS)的两个独立的非裔美国人队列(nmax=1116)中,对 SNP 进行了检测。

结果

在荟萃分析中,有 5 个多态性与血浆脂联素水平呈显著相关(P=0.035-1.02×10(-6)),包括一个低频率的精氨酸到半胱氨酸突变(R55C),可使血浆脂联素水平降低到平均值的 15%以下。然后在这些和维克森林 2 型糖尿病病例对照研究(n=3233 例 2 型糖尿病,2645 例非 2 型糖尿病)的荟萃分析中,对变体与 2 型糖尿病的相关性进行了检测。与 2 型糖尿病无关(P≥0.08),这表明 ADIPOQ 变体对 2 型糖尿病风险的影响有限。

结论

尽管鉴定出与脂联素水平相关的变体,但对 ADIPOQ 的详细遗传分析并未显示与 2 型糖尿病风险相关。这对脂联素在 2 型糖尿病发病机制中的作用提出了质疑:低脂联素水平是否真的是因果关系,还是仅仅是后果。

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