Modifiable Lifestyle Factors, Genetic Risk, and Incident Peripheral Artery Disease among Individuals with Type 2 Diabetes: A Prospective Study

医学 2型糖尿病 内科学 糖尿病 前瞻性队列研究 疾病 人口 生命银行 冠状动脉疾病 腰围 肥胖 内分泌学 生物信息学 环境卫生 生物
作者
Kai Zhu,Frank Qian,Qi Lu,Rui Li,Zixin Qiu,Lin Li,Ruyi Li,Hancheng Yu,Yulei Deng,Kun Yang,An Pan,Gang Liu
标识
DOI:10.2337/figshare.24830766
摘要

<p dir="ltr">Objectives: To prospectively evaluate the association between modifiable lifestyle factors and peripheral artery disease (PAD) among individuals with type 2 diabetes (T2D). Research design and methods: We included 14,543 individuals with T2D from the UK Biobank. We defined a weighted healthy lifestyle score using non-smoking, regular physical activity, high-quality diet, moderate alcohol consumption, optimal waist-to-hip ratio, and adequate sleep duration, and categorized into unfavorable, intermediate, and favorable lifestyle. We created a genetic risk score (GRS) using 19 SNPs previously found to be associated with PAD. We modeled the association between lifestyle score and PAD, overall and stratified by PAD genetic susceptibility. Results: After a median 13.5 years of follow-up, 628 incident cases of PAD were documented. A linear inverse association between the weighted lifestyle score and PAD was observed, with a HR (95% CI) of 0.27 (0.19, 0.38) for favorable compared to unfavorable lifestyle (Ptrend<0.0001). An estimated 58.3% (45.0%, 69.1%) of PAD in this population could be potentially avoidable if all participants attained a favorable lifestyle. Moreover, the PAD GRS was associated with increased PAD risk [HR (95%CI) per-SD increment: 1.13 (1.03, 1.23)]. A favorable lifestyle was able to partially mitigate the excess risk of PAD associated with higher GRS, albeit non-significant interaction. Several biomarkers in the lipid metabolism, hepatic/renal function, and systemic inflammation pathways collectively explained 13.3% (8.5%, 20.1%) of the association between weighted lifestyle score and PAD. Conclusion: A favorable lifestyle was associated with lower risk of PAD among individuals with T2D, independent of genetic predisposition to PAD.</p>
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