孟德尔随机化
代谢物
代谢组学
代谢组
泌尿系统
肾功能
生物标志物
人口
生物
肾脏疾病
内科学
生理学
医学
生物信息学
遗传学
内分泌学
基因型
基因
遗传变异
环境卫生
作者
Erkka Valo,Anne Richmond,Stefan Mutter,Archie Campbell,David J. Porteous,James F. Wilson,Per‐Henrik Groop,Caroline Hayward,Niina Sandholm
出处
期刊:Cold Spring Harbor Laboratory - medRxiv
日期:2023-12-21
被引量:1
标识
DOI:10.1101/2023.12.20.23300206
摘要
Abstract Dissecting the genetic mechanisms underlying urinary metabolite concentrations can provide molecular insights into kidney function and open possibilities for causal assessment of urinary metabolites with risk factors and disease outcomes. Proton nuclear magnetic resonance metabolomics provides a high-throughput means for urinary metabolite profiling, as widely applied for blood biomarker studies. Here we report a genome-wide association study meta-analysed for 3 European cohorts comprising 8,026 individuals, covering both people with type 1 diabetes and general population settings. We identified 52 associations ( p <9.3×10 -10 ) for 19 of 54 studied metabolite concentrations. Out of these, 32 were not reported previously for relevant urinary or blood metabolite traits. Subsequent two-sample Mendelian randomization analysis suggests that estimated glomerular filtration rate (eGFR) causally affects 13 urinary metabolite concentrations whereas urinary ethanolamine, an initial precursor for phosphatidylcholine and phosphatidylethanolamine, was associated with higher eGFR lending support for a potential protective role.
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