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脂联素基因常见变异与 2 型糖尿病患者的冠状动脉疾病及冠状动脉粥样硬化的血管造影严重程度相关。

Common variants in adiponectin gene are associated with coronary artery disease and angiographical severity of coronary atherosclerosis in type 2 diabetes.

机构信息

Department of Cardiology, Capital Medical University, Beijing, China.

出版信息

Cardiovasc Diabetol. 2013 Apr 17;12:67. doi: 10.1186/1475-2840-12-67.

Abstract

BACKGROUND

Adiponectin, an adipokine facilitating insulin action, has antiatherogenic effects. This study investigated whether common single nucleotide polymorphisms (SNPs) in the adiponectin gene influenced plasma adiponectin level and whether they were associated with the risk of coronary artery disease (CAD) and its angiographical severity in type 2 diabetes in Chinese population.

METHODS

11 tagging SNPs were genotyped in 1110 subjects with or without CAD in type 2 diabetes. Variants of adiponectin gene were determined by Taqman polymerase chain reaction method. The plasma adiponectin concentrations were measured by sandwich enzyme-linked immunosorbent assay. The severity and extent of coronary atherosclerosis were assessed using the angiographic Gensini score and Sullivan Extent score.

RESULTS

Among the 11 SNPs, the minor G allele of SNP rs266729 was significantly associated with higher odds of CAD (odds ratio (95% CI) = 1.49 (1.10 - 2.16), P = 0.022) after adjusting for covariates. In stepwise multivariate logistic regression, SNP rs266729 was a significant independent factor of CAD. Multivariate linear regression analysis revealed that rs266729 (β = -0.101, P < 0.0001), rs182052 (β = -0.044, P = 0.0035), and rs1501299 (β = 0.073, P < 0.0001) were significantly associated with adiponectin level, and also indicated that the minor G allele of SNP rs266729 had higher Gensini score (β = 0.139, P < 0.001) and Sullivan Extent score (β = 0.107, P < 0.001). Haplotypes analysis revealed different haplotype distributions in case and control subjects (P = 0.0003), with two common haplotypes GGG and GAG of the rs266729, rs182052, and rs1501299 being associated in heterozygotes with a greater than threefold increase in cardiovascular risk (odds ratio (95% CI)=3.39 (1.83 - 6.30), P = 0.0001).

CONCLUSIONS

In our population, genetic variants in the adiponectin gene influence plasma adiponectin levels, and one of them is a strong determinant of CAD susceptibility and its angiographical severity in type 2 diabetes. This study has provided further evidence for a role of adiponectin in the development of CAD.

摘要

背景

脂联素是一种促进胰岛素作用的脂肪因子,具有抗动脉粥样硬化作用。本研究旨在探讨中国人 2 型糖尿病患者脂联素基因常见单核苷酸多态性(SNP)是否影响血浆脂联素水平,以及它们是否与冠心病(CAD)的发病风险及其严重程度相关。

方法

在 1110 例 2 型糖尿病伴或不伴 CAD 的患者中,共检测了 11 个标记 SNP。采用 Taqman 聚合酶链反应法检测脂联素基因的变异。采用夹心酶联免疫吸附法测定血浆脂联素浓度。采用 Gensini 评分和 Sullivan 积分评估冠状动脉粥样硬化的严重程度和范围。

结果

在 11 个 SNP 中,SNP rs266729 的次要 G 等位基因与调整协变量后 CAD 的发病风险增加显著相关(比值比(95%置信区间)=1.49(1.10-2.16),P=0.022)。逐步多元逻辑回归分析显示,SNP rs266729 是 CAD 的独立危险因素。多元线性回归分析显示,rs266729(β=-0.101,P<0.0001)、rs182052(β=-0.044,P=0.0035)和 rs1501299(β=0.073,P<0.0001)与脂联素水平显著相关,并且表明 SNP rs266729 的次要 G 等位基因与更高的 Gensini 评分(β=0.139,P<0.001)和 Sullivan 积分(β=0.107,P<0.001)相关。单体型分析显示,病例组和对照组的单体型分布不同(P=0.0003),rs266729、rs182052 和 rs1501299 的常见单体型 GGG 和 GAG 在杂合子中呈不同分布,心血管风险增加三倍以上(比值比(95%置信区间)=3.39(1.83-6.30),P=0.0001)。

结论

在我们的人群中,脂联素基因的遗传变异影响血浆脂联素水平,其中一种是 2 型糖尿病患者 CAD 易感性及其血管造影严重程度的重要决定因素。本研究进一步证实了脂联素在 CAD 发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/3648457/1bacefd4b436/1475-2840-12-67-1.jpg

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