{"title":"Assessing causal associations of FGF23 and α-Klotho with urolithiasis using Mendelian randomization analysis.","authors":"Liang Chen, Li Xie, Bo Wu, Wentao Zhao","doi":"10.1007/s00240-025-01836-8","DOIUrl":null,"url":null,"abstract":"<p><p>Fibroblast growth factor 23 (FGF23) and α-Klotho may involve in the occurrence and development of urolithiasis. However, the underlying relationship is still unclear. Mendelian randomization (MR) analysis was performed on datasets from genome-wide association studies (GWASs) to investigate the causal relationship between FGF23, α-Klotho, and urolithiasis. The main focus was on determining the odds ratio (OR) using the inverse-variance weighted (IVW) approach. Reverse causal associations were also examined. IVW estimates suggested that a correlation between a heightened α-Klotho level and a reduced likelihood of kidney and ureter calculi (OR = 0.86, 95%CI: 0.81-0.92, P = 8.90e - 06), And reverse MR analysis revealed a unidirectional correlation (p > 0.05). However, no causal relationship was observed between FGF23 and urolithiasis. It was found that genetically predicted elevations in FGF23 (IVW OR = 0.98, 95%CI = 0.83-1.16) did not show any correlation with the likelihood of developing kidney and ureter calculi. We did not find any causal relationship between FGF23 and lower urinary tract stones (IVW OR = 0.91, 95%CI = 0.69-1.21, p = 0.529). There was no heterogeneity or pleiotropy evident in any of the results. Elevated levels of circulating α-Klotho may have a protective effect against kidney and ureter calculi. These findings could offer valuable insights into the underlying mechanisms involved in this pathway and help identify potential targets for preventing kidney and ureter calculi.</p>","PeriodicalId":23411,"journal":{"name":"Urolithiasis","volume":"53 1","pages":"161"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Urolithiasis","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00240-025-01836-8","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Fibroblast growth factor 23 (FGF23) and α-Klotho may involve in the occurrence and development of urolithiasis. However, the underlying relationship is still unclear. Mendelian randomization (MR) analysis was performed on datasets from genome-wide association studies (GWASs) to investigate the causal relationship between FGF23, α-Klotho, and urolithiasis. The main focus was on determining the odds ratio (OR) using the inverse-variance weighted (IVW) approach. Reverse causal associations were also examined. IVW estimates suggested that a correlation between a heightened α-Klotho level and a reduced likelihood of kidney and ureter calculi (OR = 0.86, 95%CI: 0.81-0.92, P = 8.90e - 06), And reverse MR analysis revealed a unidirectional correlation (p > 0.05). However, no causal relationship was observed between FGF23 and urolithiasis. It was found that genetically predicted elevations in FGF23 (IVW OR = 0.98, 95%CI = 0.83-1.16) did not show any correlation with the likelihood of developing kidney and ureter calculi. We did not find any causal relationship between FGF23 and lower urinary tract stones (IVW OR = 0.91, 95%CI = 0.69-1.21, p = 0.529). There was no heterogeneity or pleiotropy evident in any of the results. Elevated levels of circulating α-Klotho may have a protective effect against kidney and ureter calculi. These findings could offer valuable insights into the underlying mechanisms involved in this pathway and help identify potential targets for preventing kidney and ureter calculi.
期刊介绍:
Official Journal of the International Urolithiasis Society
The journal aims to publish original articles in the fields of clinical and experimental investigation only within the sphere of urolithiasis and its related areas of research. The journal covers all aspects of urolithiasis research including the diagnosis, epidemiology, pathogenesis, genetics, clinical biochemistry, open and non-invasive surgical intervention, nephrological investigation, chemistry and prophylaxis of the disorder. The Editor welcomes contributions on topics of interest to urologists, nephrologists, radiologists, clinical biochemists, epidemiologists, nutritionists, basic scientists and nurses working in that field.
Contributions may be submitted as full-length articles or as rapid communications in the form of Letters to the Editor. Articles should be original and should contain important new findings from carefully conducted studies designed to produce statistically significant data. Please note that we no longer publish articles classified as Case Reports. Editorials and review articles may be published by invitation from the Editorial Board. All submissions are peer-reviewed. Through an electronic system for the submission and review of manuscripts, the Editor and Associate Editors aim to make publication accessible as quickly as possible to a large number of readers throughout the world.