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  3. Deep biochemical phenotyping reveals prognostic value of rare genetic variants in adult kidney stone disease.
 

Deep biochemical phenotyping reveals prognostic value of rare genetic variants in adult kidney stone disease.

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BORIS DOI
10.48620/95928
Publisher DOI
10.1172/JCI196277
PubMed ID
41766659
Description
BACKGROUNDKidney stone disease (KSD) affects approximately 10% of the population. While genetic factors are known to play a role in KSD, determining the clinical relevance of rare variants in KSD genes identified in adults remains challenging.METHODSThe Swiss Kidney Stone Cohort is a multicenter longitudinal, observational study consisting of kidney stone formers (KSFs) (n = 701) and non-kidney stone formers (NKSFs) (n = 200). Blood and urine samples were collected at enrollment and over 3 years for deep biochemical phenotyping. Results were correlated with rare genetic variants in established KSD genes identified through whole-exome sequencing and classified according to American College of Medical Genetics and Genomics and the Association of Molecular Pathology (ACMG/AMP) criteria.RESULTSCollectively, we found rare (likely) pathogenic (LP/P) variants representing strong KSD risk factors in 6.8% of KSFs, predominantly in genes involved in renal phosphate handling and cystinuria. Detailed biochemical analyses confirmed that KSFs carrying heterozygous LP/P SLC34A3 variants exhibited significant hyperphosphaturia. In contrast, monoallelic LP/P variants in SLC34A1, SLC9A3R1, or CYP24A1, which were also frequent in NKSFs, did not result in the expected biochemical alterations, calling into question their causative role as strong KSD risk factors. In cystinuria, monoallelic SLC7A9 variants represented intermediate risk factors, since they caused biochemical alterations but required additional factors for KSD occurrence, based on frequent LP/P variants in NKSFs. The presence of strong risk factors was associated with higher kidney stone (KS) recurrence over the 3-year observation period, supporting a predictive value for genetic testing.CONCLUSIONSCorrelation of genetic findings with thorough biochemical phenotyping and comparison with NKSFs redefines the clinical relevance of variants in KSD genes and has prognostic value.
Date of Publication
2026-03-02
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
Genetics
•
Monogenic diseases
•
Nephrology
Language(s)
en
Contributor(s)
Münch, Johannes
Petrovska, Jana
Figueiro-Silva, Joana
Rubio-Aliaga, Isabel
Cabello, Elena M
Ivanovski, Ivan
Papik, Michael
Oneda, Beatrice
Fuster, Daniel G.orcid-logo
Clinic of Nephrology and Hypertension
Seeger, Harald
Ernandez, Thomas
Buchkremer, Florian
Wuerzner, Gregoire
Dhayat, Nasser A.orcid-logo
Ritter, Alexander
Segerer, Stephan
Roth, Beat
Clinic of Urology
Rauch, Anita
Ferraro, Pietro Manuel
Bonny, Olivier
Wagner, Carsten A
Bachmann-Gagescu, Ruxandra
Additional Credits
Clinic of Nephrology and Hypertension
Clinic of Urology
Series
The Journal of Clinical Investigation
Publisher
American Society for Clinical Investigation
ISSN
1558-8238
0021-9738
Related Collection(s)
MIDHOS - Metabolism I Inflammation I Digital Health I OSteology
Access(Rights)
open.access
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