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多基因风险、可改变的生活方式行为与代谢因素:与高密度脂蛋白胆固醇、甘油三酯水平及心血管风险的关联

Polygenic Risk, Modifiable Lifestyle Behaviors, and Metabolic Factors: Associations with HDL-C, Triglyceride Levels, and Cardiovascular Risk.

作者信息

Chermon Danyel, Birk Ruth

机构信息

Nutrition Department, Health Sciences Faculty, Ariel University, Ariel 40700, Israel.

出版信息

Nutrients. 2025 Jul 7;17(13):2244. doi: 10.3390/nu17132244.

Abstract

: Dyslipidemia significantly contributes to cardiovascular disease (CVD), with triglycerides (TG) and high-density lipoprotein cholesterol (HDL-C) as key components. While genetics play a key role in lipid levels, the interplay between genetic predisposition and modifiable lifestyle factors remains unexplored in population-based studies. We aimed to study the associations between weighted polygenic risk scores (wPRS) for TG and HDL-C, lifestyle, and metabolic factors with lipid traits and CVD. : In this cross-sectional study, genotype, metabolic and lifestyle data from an Israeli cohort ( = 5584 adults) were analyzed. Individual wPRSs were constructed for TG and HDL-C based on SNPs associated with each trait. Gene-environment (lifestyle and metabolic factors) associations were evaluated by stratifying participants into high wPRS (≥90th percentile) vs. lower wPRS (<90th percentile). : High wPRSs were significantly associated with unfavorable lipid profiles (higher TG and lower HDL-C) and elevated TG/HDL-C ratios. Males and females in the high wPRS had 97- and 10-fold higher odds of CVD, respectively ( < 0.0001). Individuals with a combined high wPRS and wPRS showed a 44-fold increase in CVD odds ( < 0.0001). Obesity (BMI > 30) and HbA1c ≥5.7% were significantly associated with elevated TG and reduced HDL-C levels, particularly in high wPRS and WPRS individuals, while moderate wine (1-3 drinks/week) consumption and coffee intake (≥1 cup/day) mitigated these effects, particularly among individuals with high wPRS. : Risk stratification based on genetic, lifestyle and metabolic profiles may inform personalized prevention strategies for dyslipidemia.

摘要

血脂异常是心血管疾病(CVD)的重要危险因素,甘油三酯(TG)和高密度脂蛋白胆固醇(HDL-C)是关键组成部分。虽然遗传因素在血脂水平中起关键作用,但基于人群的研究尚未探讨遗传易感性与可改变的生活方式因素之间的相互作用。我们旨在研究TG和HDL-C的加权多基因风险评分(wPRS)、生活方式和代谢因素与血脂特征及CVD之间的关联。

在这项横断面研究中,分析了来自以色列队列(n = 5584名成年人)的基因型、代谢和生活方式数据。基于与各性状相关的单核苷酸多态性(SNP)构建了TG和HDL-C的个体wPRS。通过将参与者分为高wPRS(≥第90百分位数)和低wPRS(<第90百分位数)来评估基因-环境(生活方式和代谢因素)关联。

高wPRS与不良血脂谱(高TG和低HDL-C)及升高的TG/HDL-C比值显著相关。高wPRS的男性和女性患CVD的几率分别高97倍和10倍(P < 0.0001)。高wPRS和高腰围身高比(WPRS)的个体患CVD的几率增加44倍(P < 0.0001)。肥胖(BMI > 30)和糖化血红蛋白(HbA1c)≥5.7%与TG升高和HDL-C水平降低显著相关,尤其是在高wPRS和高WPRS个体中,而适量饮酒(每周1 - 3杯)和咖啡摄入(≥1杯/天)可减轻这些影响,特别是在高wPRS个体中。

基于遗传、生活方式和代谢特征的风险分层可为血脂异常的个性化预防策略提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54cf/12252312/b2a515749a2f/nutrients-17-02244-g001.jpg

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