Gene-Lifestyle Interactions in Renal Dysfunction: Polygenic Risk Modulation via Plant-Based Diets, Coffee Intake, and Bioactive Compound Interactions.

IF 4.8 2区 医学 Q1 NUTRITION & DIETETICS
Nutrients Pub Date : 2025-03-06 DOI:10.3390/nu17050916
Meiling Liu, Da-Sol Kim, Sunmin Park
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引用次数: 0

Abstract

Background: This study aimed to investigate genetic variants associated with the estimated glomerular filtration rate (eGFR) and their interactions with lifestyle factors and bioactive compounds in large hospital-based cohorts, assessing their impact on renal dysfunction risk. Methods: Participants were categorized into two groups based on eGFR: High-GFR (control; n = 51,084) and Low-GFR (renal dysfunction; n = 7617), using an eGFR threshold of 60 mL/min/1.73 m2. Genetic variants were identified through a genome-wide association analysis, and their interactions with lifestyle factors were assessed a using generalized multifactor dimensionality reduction (GMDR) analysis. Additionally, interactions between polygenic risk scores (PRS) and nutrient intake were examined. Results: Low eGFR was associated with higher urinary protein levels (4.67-fold) and correlated with a Western-style diet and with saturated fat, arginine, and isoleucine intakes but not sodium intake. The genetic model for low eGFR included variants linked to energy production and amino acid metabolism, such as rs1047891_CPS1, rs3770636_LRP2, rs5020545_SHROOM3, rs3812036_SLC34A1, and rs4715517_HCRTR2. A high PRS was associated with a 1.78-fold increased risk of low eGFR after adjusting for sociodemographic and lifestyle factors. The PRS from the 6-SNP model interacted with plant-based diets (PBDs) and coffee intake, where individuals with higher PBD and coffee consumption had a lower risk of renal dysfunction. Additionally, CPS1 rs1047891 interacted with vitamin D intake (p = 0.0436), where the risk allele was linked to lower eGFR with low vitamin D intake but not with high intake. Molecular docking showed that vitamin D3 had a lower binding energy to the CPS1 mutant type (-9.9 kcal/mol) than the wild type (-7.5 kcal/mol), supporting a potential gene-nutrient interaction influencing renal function. Conclusions: Middle-aged and elderly individuals with a high genetic risk for renal dysfunction may benefit from a plant-based diet, moderate coffee consumption, and sufficient vitamin D intake.

肾功能障碍中的基因-生活方式相互作用:通过植物性饮食、咖啡摄入和生物活性化合物相互作用调节多基因风险。
背景:本研究旨在调查大型医院队列中与肾小球滤过率(eGFR)相关的遗传变异及其与生活方式因素和生物活性化合物的相互作用,评估其对肾功能障碍风险的影响。方法:根据eGFR将参与者分为两组:高gfr组(对照组;n = 51,084)和低gfr(肾功能不全;n = 7617), eGFR阈值为60 mL/min/1.73 m2。通过全基因组关联分析鉴定遗传变异,并使用广义多因素降维(GMDR)分析评估其与生活方式因素的相互作用。此外,还研究了多基因风险评分(PRS)与营养摄入之间的相互作用。结果:低eGFR与较高的尿蛋白水平相关(4.67倍),与西式饮食和饱和脂肪、精氨酸和异亮氨酸摄入量相关,但与钠摄入量无关。低eGFR的遗传模型包括与能量产生和氨基酸代谢相关的变异,如rs1047891_CPS1、rs3770636_LRP2、rs5020545_SHROOM3、rs3812036_SLC34A1和rs4715517_HCRTR2。在调整了社会人口统计学和生活方式因素后,高PRS与低eGFR风险增加1.78倍相关。6-SNP模型的PRS与植物性饮食(PBD)和咖啡摄入量相互作用,其中PBD和咖啡摄入量较高的个体患肾功能障碍的风险较低。此外,CPS1 rs1047891与维生素D摄入量相互作用(p = 0.0436),其中风险等位基因与低维生素D摄入量的eGFR降低有关,而与高维生素D摄入量无关。分子对接表明,维生素D3与CPS1突变型(-9.9 kcal/mol)的结合能低于野生型(-7.5 kcal/mol),支持潜在的基因-营养相互作用影响肾功能。结论:肾功能障碍遗传风险高的中老年人可能受益于植物性饮食、适量饮用咖啡和摄入足够的维生素D。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nutrients
Nutrients NUTRITION & DIETETICS-
CiteScore
9.20
自引率
15.30%
发文量
4599
审稿时长
16.74 days
期刊介绍: Nutrients (ISSN 2072-6643) is an international, peer-reviewed open access advanced forum for studies related to Human Nutrition. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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