Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.

BACKGROUND

The utility of whole-exome sequencing (WES) for the diagnosis and management of adult-onset constitutional disorders has not been adequately studied. Genetic diagnostics may be advantageous in adults with chronic kidney disease (CKD), in whom the cause of kidney failure often remains unknown.

OBJECTIVE

To study the diagnostic utility of WES in a selected referral population of adults with CKD.

DESIGN

Observational cohort.

SETTING

A major academic medical center.

PATIENTS

92 adults with CKD of unknown cause or familial nephropathy or hypertension.

MEASUREMENTS

The diagnostic yield of WES and its potential effect on clinical management.

RESULTS

Whole-exome sequencing provided a diagnosis in 22 of 92 patients (24%), including 9 probands with CKD of unknown cause and encompassing 13 distinct genetic disorders. Among these, loss-of-function mutations were identified in PARN in 2 probands with tubulointerstitial fibrosis. PARN mutations have been implicated in a short telomere syndrome characterized by lung, bone marrow, and liver fibrosis; these findings extend the phenotype of PARN mutations to renal fibrosis. In addition, review of the American College of Medical Genetics actionable genes identified a pathogenic BRCA2 mutation in a proband who was diagnosed with breast cancer on follow-up. The results affected clinical management in most identified cases, including initiation of targeted surveillance, familial screening to guide donor selection for transplantation, and changes in therapy.

LIMITATION

The small sample size and recruitment at a tertiary care academic center limit generalizability of findings among the broader CKD population.

CONCLUSION

Whole-exome sequencing identified diagnostic mutations in a substantial number of adults with CKD of many causes. Further study of the utility of WES in the evaluation and care of patients with CKD in additional settings is warranted.

PRIMARY FUNDING SOURCE

New York State Empire Clinical Research Investigator Program, Renal Research Institute, and National Human Genome Research Institute of the National Institutes of Health.