Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Peking University Centre for Public Health and Epidemic Preparedness & Response, Beijing, China.
Obesity (Silver Spring). 2023 Oct;31(10):2615-2626. doi: 10.1002/oby.23846. Epub 2023 Sep 3.
Type 2 diabetes (T2D) is caused by both genetic and cardiometabolic risk factors. However, the magnitude of the genetic predisposition of T2D in the Chinese population remains largely unknown.
This study included 93,488 participants from the China Kadoorie Biobank, and multiple polygenic risk scores (PRS) were calculated. A common cardiometabolic risk score (CRS) using smoking, alcohol consumption, physical activity, diet, obesity, blood pressure, and blood lipids was constructed to investigate the effects of cardiometabolic risk factors on T2D. Furthermore, an equation based on ideal PRS, CRS, and their interaction was established to explore the combined effects on T2D.
An ideally fitting PRS model (variance explained, R = 7.6%) was reached based on multiple PRS calculation methods. An additive interaction between PRS and CRS (coefficient = 28%, 95% CI: 0.20-0.36, p < 0.001) was found. The R of the T2D predictive model could increase to 8.3% when CRS and the interaction terms of PRS × CRS were considered. In the etiological composition of T2D, the ratio of genetic risk effect, cardiometabolic risk effect, and interaction between genetic and cardiometabolic factors was 67:16:17.
This study identified an ideally fitting PRS model for identifying and predicting the risk of T2D suitable for the Chinese population. The quantified proportional structure of genetic risk factors, cardiometabolic risk factors, and their interaction was detected, which elucidated the critical effect of genetic factors.
2 型糖尿病(T2D)是由遗传和心血管代谢危险因素共同引起的。然而,中国人群中 T2D 的遗传易感性程度在很大程度上仍不清楚。
本研究纳入了来自中国慢性病前瞻性研究的 93488 名参与者,并计算了多种多基因风险评分(PRS)。构建了一个包含吸烟、饮酒、体力活动、饮食、肥胖、血压和血脂的常见心血管代谢风险评分(CRS),以研究心血管代谢危险因素对 T2D 的影响。此外,建立了一个基于理想 PRS、CRS 及其相互作用的方程,以探讨它们对 T2D 的综合影响。
基于多种 PRS 计算方法,达到了一个理想拟合的 PRS 模型(解释方差,R2=7.6%)。发现 PRS 和 CRS 之间存在相加性交互作用(系数=28%,95%CI:0.20-0.36,p<0.001)。当考虑 CRS 和 PRS×CRS 的交互项时,T2D 预测模型的 R2 可增加到 8.3%。在 T2D 的病因构成中,遗传风险效应、心血管代谢风险效应和遗传与心血管代谢因素之间的相互作用的比例为 67:16:17。
本研究确定了一个适用于中国人群的理想的 PRS 模型,用于识别和预测 T2D 的风险。检测到遗传风险因素、心血管代谢风险因素及其相互作用的量化比例结构,阐明了遗传因素的关键作用。