Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.
Diabetes. 2013 Dec;62(12):4277-83. doi: 10.2337/db13-0129. Epub 2013 Sep 5.
Variants in the CDH13 gene have been identified as determinants of blood levels of adiponectin, an insulin-sensitizing adipokine. However, their association with other metabolic risk factors remains unclear. We examined variants at CDH13 in relation to total and high-molecular-weight (HMW) adiponectin using data from a genome-wide association study performed in 2,434 Singaporean Chinese with replication in up to 3,290 Japanese and 1,610 Koreans. The top signal rs4783244 in CDH13 showed strong associations with total adiponectin (standardized β [β] = -0.34, 95% CI -0.38 to -0.30, P = 2.0 × 10(-70)), HMW adiponectin (β = -0.40, 95% CI -0.43 to -0.36, P = 1.1 × 10(-117)), and the HMW-to-total adiponectin ratio (β = -0.44, 95% CI -0.49 to -0.40, P = 3.2 × 10(-83)). In the replication study, this single nucleotide polymorphism explained 4.1% of total and 6.5% of HMW adiponectin levels. No association was observed between rs4783244 and metabolic traits associated with insulin resistance before adjustment for HMW adiponectin levels. After adjustment for HMW adiponectin levels, the minor allele was associated with lower BMI (β = -0.15, 95% CI -0.19 to -0.11, P = 3.5 × 10(-14)), homeostasis model assessment-insulin resistance index (β = -0.16, 95% CI -0.20 to -0.12, P = 9.2 × 10(-16)), and triglycerides (β = -0.16, 95% CI -0.19 to -0.12, P = 1.3 × 10(-16)) and with higher HDL (β = 0.16, 95% CI 0.12 to 0.19, P = 2.1 × 10(-17)). CDH13 variants strongly influence plasma total and HMW adiponectin levels in East Asian populations but appear to alter adiponectin sensitivity, resulting in better metabolic health than expected based on circulating adiponectin levels.
CDH13 基因变异被认为是脂联素(一种胰岛素增敏脂肪因子)血水平的决定因素。然而,它们与其他代谢风险因素的关联仍不清楚。我们使用在 2434 名新加坡华人中进行的全基因组关联研究的数据,以及在最多 3290 名日本人(Japanese)和 1610 名韩国人中进行的复制研究,来研究 CDH13 中的变异与总脂联素和高分子量(HMW)脂联素的关系。在 CDH13 中的最显著信号 rs4783244 与总脂联素(标准化β[β] = -0.34,95%置信区间 -0.38 至 -0.30,P = 2.0×10(-70)),HMW 脂联素(β = -0.40,95%置信区间 -0.43 至 -0.36,P = 1.1×10(-117))和 HMW 与总脂联素的比值(β = -0.44,95%置信区间 -0.49 至 -0.40,P = 3.2×10(-83))具有强烈关联。在复制研究中,这种单核苷酸多态性解释了总脂联素和 HMW 脂联素水平的 4.1%和 6.5%。在调整 HMW 脂联素水平之前,rs4783244 与胰岛素抵抗相关的代谢特征之间没有关联。在调整 HMW 脂联素水平后,与较低的 BMI(β = -0.15,95%置信区间 -0.19 至 -0.11,P = 3.5×10(-14)),稳态模型评估胰岛素抵抗指数(β = -0.16,95%置信区间 -0.20 至 -0.12,P = 9.2×10(-16))和甘油三酯(β = -0.16,95%置信区间 -0.19 至 -0.12,P = 1.3×10(-16))以及较高的高密度脂蛋白(β = 0.16,95%置信区间 0.12 至 0.19,P = 2.1×10(-17))相关。CDH13 变异在东亚人群中强烈影响血浆总脂联素和 HMW 脂联素水平,但似乎改变了脂联素的敏感性,导致代谢健康状况优于根据循环脂联素水平预期的水平。