College of Public Health, Zhengzhou University, Zhengzhou, NO.100 Kexue Road, High-Tech Development Zone of States, People's Republic of China.
Department of Geriatrics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, People's Republic of China.
Eur J Hum Genet. 2018 Oct;26(10):1547-1553. doi: 10.1038/s41431-018-0180-9. Epub 2018 Jun 11.
Adiposity has been associated with the risk of coronary artery disease (CAD) in observational studies, but their association may differ according to specific characteristics of studies. In Mendelian randomization (MR) analyses, genetic variants are used as instrumental variables (IVs) of exposures to examine causal effects to overcome confounding factors and reverse causation. We performed MR analyses for adiposity (n = 322,154) on risk of CAD (60,801 cases and 123,504 controls) based on the currently largest genome-wide association studies. The estimated associations between adiposity traits and CAD were calculated by an inverse-variance weighted method with and without excluding the IVs, which are associated with the well-known risk factors of CAD. Genetic variants are identified to be associated with the well-known risk factors of CAD by a cross-phenotype meta-analysis method. Our results furnished strong evidence for a causal role of adiposity in risk of CAD, with the odds ratios (ORs) for CAD being 1.53 (95% CI 1.36-1.72) for body mass index (BMI), 1.48 (1.20-1.96) for waist-hip ratio (WHR), and 1.34 (1.07-1.59) for WHR adjusted for BMI (WHRadjBMI), respectively. After excluding mediators-associated IVs from the MR analyses, the corresponding ORs were 1.46 (1.28-1.67) for BMI, 1.39 (1.01-1.93) for WHR, and 1.38 (1.04-1.84) for WHRadjBMI, respectively. Furthermore, our results suggested that central adiposity and general adiposity might pose a similar risk for CAD. In summary, our data supported that genetically driven adiposity traits imposed the risk of CAD independent of blood pressure, dyslipidaemia, glycaemic traits, and type 2 diabetes.
肥胖与冠心病(CAD)的风险在观察性研究中相关,但它们的关联可能因研究的具体特征而异。在孟德尔随机化(MR)分析中,遗传变异被用作暴露的工具变量(IV),以检查因果效应,以克服混杂因素和反向因果关系。我们基于目前最大的全基因组关联研究,对 322154 名肥胖者(60801 例 CAD 病例和 123504 例对照)进行了 CAD 风险的 MR 分析。通过逆方差加权法计算了肥胖特征与 CAD 之间的估计关联,并在不排除与 CAD 已知危险因素相关的 IVs 的情况下进行了计算。通过跨表型荟萃分析方法,确定与 CAD 已知危险因素相关的遗传变异。我们的结果为肥胖与 CAD 风险之间存在因果关系提供了强有力的证据,体质量指数(BMI)的 CAD 比值比(OR)为 1.53(95%CI 1.36-1.72),腰围-臀围比(WHR)为 1.48(1.20-1.96),WHR 校正 BMI 后(WHRadjBMI)为 1.34(1.07-1.59)。在 MR 分析中排除与中介物相关的 IVs 后,对应的 OR 分别为 1.46(1.28-1.67)、1.39(1.01-1.93)和 1.38(1.04-1.84)。此外,我们的结果表明,中心性肥胖和全身性肥胖可能对 CAD 构成相似的风险。总之,我们的数据支持遗传驱动的肥胖特征独立于血压、血脂异常、血糖特征和 2 型糖尿病,增加 CAD 的风险。