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Genotype-phenotype correlations and clinical outcomes of genetic TRPC6 podocytopathies

Title: Genotype-phenotype correlations and clinical outcomes of genetic TRPC6 podocytopathies
Authors: Mcanallen SM; Elhassan EAE; Stoneman S; Vairo FPE; Hogan MC; Hoefele J; Clince M; Mekraksakit P; Titan SM; Jorge S; Calado J; Decramer S; Colliou E; Tellier S; Francisco T; Servais A; Cornet J; De Fallois J; Dossier C; Fenoglio R; Renieri A; Pinto AM; Daga S; Loberti L; Fila M; Quintana LF; Becherucci F; Godefroid N; Dubrasquet A; Kalman T; Dolan N; Alawi BA; Sweeney C; Riordan M; Stack M; Awan A; Hui NK; Mccarthy HJ; Biros E; Harris T; Kidd K; Haeberle S; Bleyer AJ; Mallett AJ; Sayer JA; Schafer F; Benson KA; Mccann E; Conlon PJ
Source: Nephrology Dialysis Transplantation, 1 January 2026
Publisher Information: Oxford University Press
Publication Year: 2026
Collection: Newcastle University Library ePrints Service
Description: © 2025 The Author(s).Background and hypothesis Podocytopathy associated with likely pathogenic/pathogenic variants of Transient receptor potential cation channel subfamily C member 6 (TRPC6) (TRPC6-AP) has been recognized for about 20 years. As a result of its rarity however, the spectrum of clinical phenotypes and genotype-phenotype correlation of TRPC6-AP remains poorly understood. Here, we characterized clinical, histological and genetic correlates of familial and sporadic patients with TRPC6-AP. Methods In this multicentre observational study, an online questionnaire followed by a systematic literature review was performed to create a cohort with comprehensive data on genetic and clinical outcomes [age of onset, clinical presentation, treatment response, kidney biopsy findings and progression to kidney failure (KF)]. Logistic regression, Cox proportional hazards model and Kaplan-Meier analyses investigated the associations between genetic variants and disease progression. Results Among 87 families (96 familial and 45 sporadic cases), 31 distinct missense TRPC6 variants (including 2 novel) were identified, with c.2683C>T p.(Arg895Cys) and c.523C>T p.(Arg175Trp) the commonest variants. Proteinuric kidney disease/nephrotic syndrome was the most common clinical presentation (83.7%), while focal segmental glomerulosclerosis was the most common histological finding (89.4%). By 33 (interquartile range 17-40) years, 48.9% (69/141) of patients had progressed to KF. Sporadic TRPC6-AP demonstrated an earlier progression to KF than familial cases (P =. 001) and were more likely to present with nephrotic syndrome [odds ratio 4.34 (1.85-10.15); P =. 001]. Gain-of-function TRPC6 variants were more frequent in familial than sporadic TRPC6-AP (70.8% vs 44.4%; P =. 004). Compared with patients with other TRPC6 variants, patients with TRPC6 p.R175W and p.R895C variants progressed to KF earlier [median kidney survival of 21 years, hazard ratio 2.985 (95% confidence interval 1.40-5.79); and 38 years, hazard ratio 1.65 (95% ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/309637; https://eprints.ncl.ac.uk/fulltext.aspx?url=309637/95647003-E9B4-45B6-9CD7-74CB3A702E1B.pdf&pub_id=309637
Availability: https://eprints.ncl.ac.uk/309637
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.5EEAC898
Database: BASE