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Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
- 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.
- Subjects :
- Adult
Genetic Markers
Male
0301 basic medicine
Pediatrics
medicine.medical_specialty
Candidate gene
Heredity
Nephrotic Syndrome
Adolescent
Epidemiology
DNA Mutational Analysis
Medizin
030232 urology & nephrology
Critical Care and Intensive Care Medicine
Young Adult
03 medical and health sciences
0302 clinical medicine
Mutation Rate
Predictive Value of Tests
Exome Sequencing
medicine
Humans
Genetic Predisposition to Disease
Age of Onset
Child
Exome
Congenital nephrotic syndrome
Genetic Association Studies
Exome sequencing
Phenocopy
Transplantation
business.industry
Infant
Original Articles
Prognosis
medicine.disease
Pedigree
Steroid-resistant nephrotic syndrome
Phenotype
030104 developmental biology
Nephrology
Child, Preschool
Mutation
Female
Age of onset
business
Nephrotic syndrome
Subjects
Details
- ISSN :
- 1555905X and 15559041
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- Clinical Journal of the American Society of Nephrology
- Accession number :
- edsair.doi.dedup.....d15411e30c773cf5cd62db0ecbe78cbb
- Full Text :
- https://doi.org/10.2215/cjn.04120417