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Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

Authors :
Heon Yung Gee
Richard P. Lifton
Aytül Noyan
Stefan Kohl
Weizhen Tan
Michael A. J. Ferguson
Neveen A. Soliman
Deborah R. Stein
Jing Chen
Svjetlana Lovric
J. Magdalena Schmidt
Jameela A. Kari
Avram Z. Traum
Jia Rao
Gil Chernin
Sherif El Desoky
Radovan Bogdanovic
Nadine Benador
Werner L. Pabst
Hanan M. Fathy
Jeffrey B. Kopp
Jillian K. Warejko
Asaf Vivante
Henry Fehrenbach
Detlef Bockenhauer
Carolin E. Sadowski
Velibor Tasic
Robert B. Ettenger
Amelie T. van der Ven
Shrikant Mane
Ankana Daga
Jeffrey Hopcian
Martin Zenker
Markus J. Kemper
Amar J. Majmundar
Erkin Serdaroglu
Ronen Schneider
Fatih Ozaltin
Ghaleb Daouk
Natasa Stajic
Nancy Rodig
Jennifer A. Lawson
Reyner Loza Munarriz
Melissa A. Cadnapaphornchai
Hadas Ityel
Shazia Ashraf
Rainer Büscher
Dominik N. Müller
Makiko Nakayama
Michelle A. Baum
Seema Hashmi
Ludmila Podracka
David Schapiro
Daniela A. Braun
Shirlee Shril
Michael J. Somers
Eugen Widmeier
Tilman Jobst-Schwan
Friedhelm Hildebrandt
Sevcan A. Bakkaloglu
Tobias Hermle
Source :
Clinical Journal of the American Society of Nephrology. 13:53-62
Publication Year :
2017
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2017.

Abstract

Background and objectives Steroid-resistant nephrotic syndrome overwhelmingly progresses to ESRD. More than 30 monogenic genes have been identified to cause steroid-resistant nephrotic syndrome. We previously detected causative mutations using targeted panel sequencing in 30% of patients with steroid-resistant nephrotic syndrome. Panel sequencing has a number of limitations when compared with whole exome sequencing. We employed whole exome sequencing to detect monogenic causes of steroid-resistant nephrotic syndrome in an international cohort of 300 families. Design, setting, participants, & measurements Three hundred thirty-five individuals with steroid-resistant nephrotic syndrome from 300 families were recruited from April of 1998 to June of 2016. Age of onset was restricted to Results In 74 of 300 families (25%), we identified a causative mutation in one of 20 genes known to cause steroid-resistant nephrotic syndrome. In 11 families (3.7%), we detected a mutation in a gene that causes a phenocopy of steroid-resistant nephrotic syndrome. This is consistent with our previously published identification of mutations using a panel approach. We detected a causative mutation in a known steroid-resistant nephrotic syndrome gene in 38% of consanguineous families and in 13% of nonconsanguineous families, and 48% of children with congenital nephrotic syndrome. A total of 68 different mutations were detected in 20 of 33 steroid-resistant nephrotic syndrome genes. Fifteen of these mutations were novel. NPHS1, PLCE1, NPHS2, and SMARCAL1 were the most common genes in which we detected a mutation. In another 28% of families, we detected mutations in one or more candidate genes for steroid-resistant nephrotic syndrome. Conclusions Whole exome sequencing is a sensitive approach toward diagnosis of monogenic causes of steroid-resistant nephrotic syndrome. A molecular genetic diagnosis of steroid-resistant nephrotic syndrome may have important consequences for the management of treatment and kidney transplantation in steroid-resistant nephrotic syndrome.

Details

ISSN :
1555905X and 15559041
Volume :
13
Database :
OpenAIRE
Journal :
Clinical Journal of the American Society of Nephrology
Accession number :
edsair.doi.dedup.....d15411e30c773cf5cd62db0ecbe78cbb