Evidence map›Paper›PMID 40646443›Full record

ArticleGenes & nutrition2025

The impact of beverage consumption on chronic renal failure risk and the mediation of serum metabolites: based on Mendelian randomization study.

Zhengshu Wei, Dunsheng Mo, Wenxin Lü, Shangxin Wu, Yan Zhang, Zhen Tang, Yongyi Fan

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Article in Genes & nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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7 authors.

Zhengshu Wei *Liuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China.
Dunsheng Mo *Liuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China.
Wenxin LüLiuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China.
Shangxin WuLiuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China.
Yan ZhangLiuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China.
Zhen TangLiuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China.
Yongyi FanLiuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University, Guangxi, 545005, China. yz_723@163.com.

Funding

The self -financing research of the health department of Guangxi autonomous region Z20200986,Z20210478
6 · The paper itself

Abstract

backgroundChronic renal failure (CRF), the end-stage of chronic kidney disease, affects approximately 10% of the global population. While associations between beverage consumption and renal function have been reported, their causal relationships remain unclear. This study aimed to investigate the causal relationships between different beverage consumption and CRF, as well as the mediating effects of serum metabolites.

methodsUsing a two-sample Mendelian randomization (MR) approach, we analyzed genetic data from the UK Biobank and GWAS databases. We examined bidirectional causal relationships between water, coffee, tea, and alcohol consumption with CRF, and screened metabolites significantly associated with CRF from 1,400 metabolites for mediation analysis. Additionally, we evaluated the mediating effects of these metabolites in the relationship between beverage consumption and CRF.

resultsMR analysis showed evidence for a causal association between tea consumption and reduced CRF risk (OR = 0.314, 95% CI: 0.155-0.634, p = 0.001), while alcohol consumption was causally associated with increased CRF risk (OR = 1.275, 95% CI: 1.046-1.553, p = 0.016). Water and coffee consumption showed no significant associations with CRF. Further analysis identified 11 metabolites significantly associated with CRF. Salicylate demonstrated a positive mediating effect (12.5%) in the association between tea consumption and CRF risk, while 3-methyl catechol sulfate (-25.70%), glutarate (C5-DC) (-14.60%), and X-23,655 (-18.7%) showed negative mediating effects. In the alcohol consumption-CRF pathway, the ornithine-to-phosphate ratio exhibited a positive mediating effect, while X-23,655 showed a negative mediating effect.

conclusionThis study provides evidence for a potential protective association of tea consumption and a potential harmful association of alcohol consumption with CRF risk, partially mediated through specific serum metabolites. These findings contribute new insights into potential CRF prevention strategies and may inform dietary guidelines.

Indexed as

AlcoholChronic renal failureCoffeeMendelian randomizationMetabolitesTea

Identifiers

PMID40646443
PMCPMC12247210

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.