Translating genetic findings in hereditary nephrotic syndrome: the missing loops.

Published

Journal Article (Review)

Nephrotic syndrome (NS) is a clinicopathological entity characterized by proteinuria, hypoalbuminemia, peripheral edema, and hyperlipidemia. It is the most common cause of glomerular disease in children and adults. Although the molecular pathogenesis of NS is not completely understood, data from the study of familial NS suggest that it is a "podocytopathy." Virtually all of the genes mutated in hereditary NS localize to the podocyte or its secreted products and the slit diaphragm. Since the completion of human genome sequence and the advent of next generation sequencing, at least 29 causes of single-gene NS have been identified. However, these findings have not been matched by therapeutic advances owing to suboptimal in vitro and in vivo models for the study of human glomerular disease and podocyte injury phenotypes. Multidisciplinary collaboration between clinicians, geneticists, cell biologists, and molecular physiologists has the potential to overcome this barrier and thereby speed up the translation of genetic findings into improved patient care.

Full Text

Duke Authors

Cited Authors

  • Hall, G; Gbadegesin, RA

Published Date

  • July 1, 2015

Published In

Volume / Issue

  • 309 / 1

Start / End Page

  • F24 - F28

PubMed ID

  • 25810439

Pubmed Central ID

  • 25810439

Electronic International Standard Serial Number (EISSN)

  • 1522-1466

Digital Object Identifier (DOI)

  • 10.1152/ajprenal.00683.2014

Language

  • eng

Conference Location

  • United States