Evidence map›Paper›PMID 42002888›Full record

ArticleRenal failure2026

Kidney function decline and kidney stone risk: cohort and Mendelian randomization analyses.

Chi Yuan, Linna Sha, Baoyun Xue, Xia Jiang, Zhongyu Jian

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Article in Renal failure, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Chi YuanDepartment of Pediatric Surgery, Department of Urology, Institute of Urology (Laboratory of Reconstructive Urology), West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0009-0008-3003-7409
Linna ShaDepartment of Nutrition and Food Hygiene, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0009-0005-7117-8804
Baoyun XueDepartment of Urology, Institute of Urology (Laboratory of Reconstructive Urology), West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0009-0000-2844-4218
Xia JiangDepartment of Nutrition and Food Hygiene, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0000-0001-5878-8986
Zhongyu JianDepartment of Urology, Institute of Urology (Laboratory of Reconstructive Urology), West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0000-0002-8532-9336

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the association and potential causal effect of kidney function decline on kidney stone disease (KSD).

methodsWe evaluated linear and non-linear associations between kidney function decline-assessed by estimated glomerular filtration rate (eGFR) and chronic kidney disease (CKD)-and KSD using individual-level data from the UK Biobank and summary genome-wide association study (GWAS) data. Analyses included prospective cohort models, one-sample Mendelian randomization (MR), two-sample MR, genetic correlation analyses, and identification of shared single-nucleotide polymorphisms (SNPs).

resultsIndividuals with lower baseline eGFR_cys had an increased risk of KSD during a mean follow-up of 13.9 years. However, longitudinal decline in eGFR over time (ΔeGFR_cys) was associated with a reduced risk of KSD (HR 0.80, 95% CI 0.67-0.95). Mendelian randomization analyses showed that genetically predicted lower eGFR (one-sample: OR 0.70, 95% CI 0.63-0.78; two-sample: OR 0.78, 95% CI 0.71-0.85) and CKD (one-sample: OR 0.73, 95% CI 0.65-0.81; two-sample: OR 0.89, 95% CI 0.83-0.97) were associated with a lower risk of KSD. Genetic correlation analyses suggested shared genetic influences between kidney function traits and KSD (eGFR: r

conclusionsKidney function decline appears to be associated with a reduced risk of KSD. Combined observational and genetic analyses support shared biological pathways linking these conditions, although further studies are needed to clarify the underlying mechanisms.

Indexed as

Glomerular Filtration RateKidneyKidney CalculiRenal Insufficiency, ChronicAgedFemaleGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisMiddle AgedPolymorphism, Single NucleotideProspective StudiesRisk FactorsUK BiobankUnited Kingdomchronic kidney diseaseEstimated glomerular filtration rategenetic correlationkidney stone diseaseMendelian RandomizationUK biobank

Identifiers

PMID42002888
PMCPMC13097174

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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.