Department of Medicine, University Health Network, Toronto & University of Toronto, Toronto, Ontario, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, Ontario, Canada.
Diabetes Obes Metab. 2024 Jun;26(6):2284-2291. doi: 10.1111/dom.15542. Epub 2024 Mar 15.
Increased waist/hip ratio (WHR) contributes to type 2 diabetes, fatty liver, dyslipidaemia, hypertension and coronary artery disease, with potential sex-differential effects. Postulated mediators include increased lipid flux, branched-chain amino acids, glycine and glycoprotein acetyl, but their relative contributions and sex-specific impact on WHR-associated cardiometabolic disease (CMD) are not established.
We therefore undertook combined and sex-stratified Mendelian randomization (MR) to assess the relative causal contributions of these mediators to WHR-associated CMD using summary statistics from the largest genome-wide association studies in European ancestries.
In sex-combined MR analyses, increased WHR significantly reduces high-density lipoprotein (beta = -0.416, SE = 0.029, p = 2.87E-47), increases triglyceride (beta = 0.431, SE = 0.029, p = 1.87E-50), type 2 diabetes (odds ratio = 2.747, SE = 0.09, p = 26E-23), coronary artery disease (odds ratio = 1.478, SE = 0.045, p = 6.96E-18), alanine transaminase (beta = 0.062, SE = 0.004, p = 6.88E-67), and systolic (beta = 0.134, SE = 0.022, p = 7.81E-10) and diastolic blood pressure (beta = 0.162, SE = 0.026, p = 5.38E-10). Adjustment for the mediators attenuated WHR's effects, but the associations remained significant with concordant results in females. In males, a similar pattern was seen, except after adjusting for the effect of the ratio of monounsaturated fatty acid to total free fatty acid, the potential causal effect of WHR was no longer significant: high-density lipoprotein (beta = -0.117, SE = 0.069, p = .09) and triglyceride (beta = 0.051, SE = 0.068, p = .459).
MR suggests WHR increases the risk of CMD independent of these mediators, with the exception of dyslipidaemia in males, which is largely driven by the monounsaturated fatty acid to total free fatty acid ratio.
腰围/臀围比值(WHR)的增加与 2 型糖尿病、脂肪肝、血脂异常、高血压和冠状动脉疾病有关,且可能存在性别差异的影响。推测的中介物包括脂质通量增加、支链氨基酸、甘氨酸和糖蛋白乙酰化,但它们对 WHR 相关代谢性心血管疾病(CMD)的相对贡献及其对性别的影响尚未确定。
因此,我们进行了联合和性别分层的孟德尔随机化(MR)分析,以使用欧洲血统最大的全基因组关联研究的汇总统计数据评估这些介质对 WHR 相关 CMD 的相对因果贡献。
在性别混合 MR 分析中,WHR 增加显著降低高密度脂蛋白(β=-0.416,SE=0.029,p=2.87E-47),增加甘油三酯(β=0.431,SE=0.029,p=1.87E-50),2 型糖尿病(比值比=2.747,SE=0.09,p=26E-23),冠状动脉疾病(比值比=1.478,SE=0.045,p=6.96E-18),丙氨酸转氨酶(β=0.062,SE=0.004,p=6.88E-67),收缩压(β=0.134,SE=0.022,p=7.81E-10)和舒张压(β=0.162,SE=0.026,p=5.38E-10)。中介物的调整减弱了 WHR 的影响,但在女性中,相关性仍然显著,且结果一致。在男性中,除了调整单不饱和脂肪酸与游离脂肪酸总量的比值后,WHR 的潜在因果效应不再显著外,观察到类似的模式:高密度脂蛋白(β=-0.117,SE=0.069,p=0.09)和甘油三酯(β=0.051,SE=0.068,p=0.459)。
MR 表明,WHR 增加了 CMD 的风险,而这些介质则不是主要因素,除了男性的血脂异常,这主要是由单不饱和脂肪酸与游离脂肪酸总量的比值驱动的。