Genomic Testing in Patients with Kidney Failure of an Unknown Cause: a National Australian Study.


Journal

Clinical journal of the American Society of Nephrology : CJASN
ISSN: 1555-905X
Titre abrégé: Clin J Am Soc Nephrol
Pays: United States
ID NLM: 101271570

Informations de publication

Date de publication:
03 May 2024
Historique:
received: 30 10 2023
accepted: 25 04 2024
medline: 11 6 2024
pubmed: 11 6 2024
entrez: 11 6 2024
Statut: aheadofprint

Résumé

The cause of kidney failure is unknown in approximately 10% of patients with stage 5 chronic kidney disease (CKD). For those who first present to nephrology care with kidney failure, standard investigations of serology, imaging, urinalysis and kidney biopsy are limited differentiators of etiology. We aimed to determine the diagnostic utility of whole-genome sequencing (WGS) with analysis of a broad kidney gene panel in patients with kidney failure of unknown cause. We prospectively recruited 100 participants who reached CKD stage 5 at 50 years of age and had an unknown cause of kidney failure after standard investigation. Clinically-accredited WGS was performed in this national cohort after genetic counselling. The primary analysis was targeted to 388 kidney-related genes with second-tier genome-wide and mitochondrial analysis. The cohort was 61% male and the average age of participants at stage 5 CKD was 32 years (9 months to 50 years). A genetic diagnosis was made in 25% of participants. Disease-causing variants were identified across autosomal dominant tubulointerstitial kidney disease (6), glomerular disorders (4), ciliopathies (3), tubular disorders (2), Alport syndrome (4) and mitochondrial disease (1). Most diagnoses (80%) were in autosomal dominant, X-linked or mitochondrial conditions (UMOD; COL4A5; INF2; CLCN5; TRPC6; COL4A4; EYA1; HNF1B; WT1; NBEA; m.3243A>G). Patients with a family history of CKD were more likely to have a positive result (OR 3.29, 95% CI 1.10-11.29). Thirteen percent of participants without a CKD family history had a positive result. In those who first presented in stage 5 CKD, WGS with broad analysis of a curated kidney-disease gene panel was diagnostically more informative than kidney biopsy, with biopsy being inconclusive in 24 of 25 participants. In this prospectively ascertained Australian cohort, we identified a genetic diagnosis in 25% of patients with kidney failure of unknown cause.

Sections du résumé

BACKGROUND BACKGROUND
The cause of kidney failure is unknown in approximately 10% of patients with stage 5 chronic kidney disease (CKD). For those who first present to nephrology care with kidney failure, standard investigations of serology, imaging, urinalysis and kidney biopsy are limited differentiators of etiology. We aimed to determine the diagnostic utility of whole-genome sequencing (WGS) with analysis of a broad kidney gene panel in patients with kidney failure of unknown cause.
METHODS METHODS
We prospectively recruited 100 participants who reached CKD stage 5 at 50 years of age and had an unknown cause of kidney failure after standard investigation. Clinically-accredited WGS was performed in this national cohort after genetic counselling. The primary analysis was targeted to 388 kidney-related genes with second-tier genome-wide and mitochondrial analysis.
RESULTS RESULTS
The cohort was 61% male and the average age of participants at stage 5 CKD was 32 years (9 months to 50 years). A genetic diagnosis was made in 25% of participants. Disease-causing variants were identified across autosomal dominant tubulointerstitial kidney disease (6), glomerular disorders (4), ciliopathies (3), tubular disorders (2), Alport syndrome (4) and mitochondrial disease (1). Most diagnoses (80%) were in autosomal dominant, X-linked or mitochondrial conditions (UMOD; COL4A5; INF2; CLCN5; TRPC6; COL4A4; EYA1; HNF1B; WT1; NBEA; m.3243A>G). Patients with a family history of CKD were more likely to have a positive result (OR 3.29, 95% CI 1.10-11.29). Thirteen percent of participants without a CKD family history had a positive result. In those who first presented in stage 5 CKD, WGS with broad analysis of a curated kidney-disease gene panel was diagnostically more informative than kidney biopsy, with biopsy being inconclusive in 24 of 25 participants.
CONCLUSIONS CONCLUSIONS
In this prospectively ascertained Australian cohort, we identified a genetic diagnosis in 25% of patients with kidney failure of unknown cause.

Identifiants

pubmed: 38861662
doi: 10.2215/CJN.0000000000000464
pii: 01277230-990000000-00377
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Health and Medical Research Council
ID : GNT1113531
Organisme : National Health and Medical Research Council
ID : GNT2000001
Organisme : National Health and Medical Research Council
ID : MRF2008820
Organisme : National Health and Medical Research Council
ID : MRF2008249

Informations de copyright

Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology.

Auteurs

Amali C Mallawaarachchi (AC)

Clinical Genetics Service, Institute of Precision Medicine and Bioinformatics, Royal Prince Alfred Hospital, Sydney, Australia.
Genomic and Inherited Diseases Program, Garvan Institute of Medical Research, Sydney, Australia.
KidGen Collaborative, Australian Genomics Health Alliance, Murdoch Children's Research Institute, Melbourne, Australia.

Lindsay Fowles (L)

Genetic Health Queensland, Royal Brisbane and Women's Hospital, Herston QLD, Australia.

Louise Wardrop (L)

KidGen Collaborative, Kidney Regeneration, Murdoch Children's Research Institute.

Alasdair Wood (A)

KidGen Collaborative, Kidney Regeneration, Murdoch Children's Research Institute.

Rosie O'Shea (R)

KidGen Collaborative, Australian Genomics Health Alliance, Murdoch Children's Research Institute, Melbourne, Australia.

Erik Biros (E)

KidGen Collaborative, Australian Genomics Health Alliance, Murdoch Children's Research Institute, Melbourne, Australia.
College of Medicine & Dentistry, James Cook University, Townsville, Queensland, Australia.
Townsville University Hospital, Townsville, Queensland, Australia.

Trudie Harris (T)

KidGen Collaborative, Australian Genomics Health Alliance, Murdoch Children's Research Institute, Melbourne, Australia.
Townsville University Hospital, Townsville, Queensland, Australia.

Stephen I Alexander (SI)

Centre for Kidney Research at the Children's Hospital at Westmead, NSW, Australia.
Department of Nephrology, Children's Hospital at Westmead, Sydney, Australia.
Discipline of Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, NSW, Australia.

Simon Bodek (S)

Clinical Genetics Service, Austin Health, Melbourne, Australia.

Neil Boudville (N)

Medical School, University of Western Australia, WA, Australia.

Jo Burke (J)

School of Medicine and Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.
Tasmanian Clinical Genetics Service, Royal Hobart Hospital, Tasmania, Australia.

Leslie Burnett (L)

Genomic and Inherited Diseases Program, Garvan Institute of Medical Research, Sydney, Australia.
Northern Clinical School, Faculty of Medicine and Health, University of Sydney.
St Vincent's Healthcare Clinical Campus, UNSW Sydney.

Sarah Casauria (S)

Australian Genomics, Murdoch Children's Research Institute, Melbourne, Australia.

Steve Chadban (S)

Renal Medicine, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

Aron Chakera (A)

Harry Perkins Institute for Medical Research, University of Western Australia and UWA.
Renal Unit, Sir Charles Gairdner Hospital, Nedlands 6009, Western Australia.

Sam Crafter (S)

The Women's and Children's Hospital, South Australia, Australia.

Pei Dai (P)

Precision Immunology Program, Garvan Institute of Medical Research, Sydney, Australia.
St Vincent's Clinical School, Faculty of Medicine, UNSW Sydney, Sydney, Australia.

Paul De Fazio (P)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.

Randall Faull (R)

Renal Unit, Royal Adelaide Hospital, SA, Australia.
University of Adelaide, SA, Australia.

Andrew Honda (A)

The Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Sydney, Australia.

Vanessa Huntley (V)

Adult Genetics Service, Royal Adelaide Hospital, SA, Australia.

Sadia Jahan (S)

The Central and Northern Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, Australia.

Kushani Jayasinghe (K)

Department of Medicine, Monash University, Melbourne, Australia.
Department of Nephrology, Monash Health, Melbourne, Australia.
Melbourne Health, Melbourne, Australia.

Matthew Jose (M)

Royal Hobart Hospital, Tasmania, Australia.

Anna Leaver (A)

Clinical Genetics Service, Austin Health, Melbourne, Australia.

Mandi MacShane (M)

Genetic Services of WA, KEMH, Subiaco WA, Australia.
Harry Perkins Institute of Medical Research, Nedlands WA, Australia.

Evanthia Olympia Madelli (EO)

Australian Genomics, Murdoch Children's Research Institute, Melbourne, Australia.

Kathy Nicholls (K)

Nephrology Unit Royal Melbourne Hospital Parkville Australia.
The University of Melbourne Parkville, Australia.

Rhonda Pawlowski (R)

Anatomical Pathology, Monash Health, Melbourne, Australia.

Gopi Rangan (G)

Department of Renal Medicine, Westmead Hospital, Western Sydney Local Health District, Australia.
Michael Stern Laboratory for Polycystic Kidney Disease, Westmead Institute for Medical Research, Australia.

Paul Snelling (P)

Renal Medicine, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

Jacqueline Soraru (J)

Department of Nephrology and Hypertension, Perth Children's Hospital, Perth, Australia.
Department of Nephrology and Renal Transplantation, Fiona Stanley Hospital, Perth, Australia.

Madhivanan Sundaram (M)

Royal Darwin Hospital, Northern Territory, Australia.

Michel Tchan (M)

Genetic Medicine, Westmead Hospital, Sydney NSW, Australia.
Sydney Medical School, University of Sydney, Australia.

Giulia Valente (G)

Clinical Genetics Service, Austin Health, Melbourne, Australia.

Mathew Wallis (M)

School of Medicine and Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.
Tasmanian Clinical Genetics Service, Royal Hobart Hospital, Tasmania, Australia.
Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.

Laura Wedd (L)

Centre for Population Genomics, Garvan Institute of Medical Research and UNSW Sydney, Sydney, Australia.

Matthew Welland (M)

Centre for Population Genomics, Garvan Institute of Medical Research and UNSW Sydney, Sydney, Australia.
Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Australia.

John Whitlam (J)

Department of Nephrology, Austin Health, Melbourne, Australia.

Ella J Wilkins (EJ)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.

Hugh McCarthy (H)

Centre for Kidney Research at the Children's Hospital at Westmead, NSW, Australia.
Discipline of Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, NSW, Australia.
Department of Nephrology, Sydney Children's Hospitals Network, NSW, Australia.

Cas Simons (C)

Centre for Population Genomics, Garvan Institute of Medical Research and UNSW Sydney, Sydney, Australia.
Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Australia.
Department of Kidney Regeneration, Murdoch Children's Research Institute, Melbourne, Australia.

Catherine Quinlan (C)

Department of Kidney Regeneration, Murdoch Children's Research Institute, Melbourne, Australia.
Department of Nephrology, Royal Children's Hospital, Melbourne, Australia.
Department of Paediatrics, University of Melbourne, Australia.

Chirag Patel (C)

Genetic Health Queensland, Royal Brisbane and Women's Hospital, Herston QLD, Australia.

Zornitza Stark (Z)

Australian Genomics, Murdoch Children's Research Institute, Melbourne, Australia.
Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.
Department of Paediatrics, University of Melbourne, Australia.

Andrew Mallett (A)

KidGen Collaborative, Australian Genomics Health Alliance, Murdoch Children's Research Institute, Melbourne, Australia.
Townsville University Hospital, Townsville, Queensland, Australia.
Australian Genomics, Murdoch Children's Research Institute, Melbourne, Australia.
Institute for Molecular Bioscience and Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

Classifications MeSH