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The Genetics of Diabetic Nephropathy

Up to 40% of patients with type 1 and type 2 diabetes will develop diabetic nephropathy (DN), resulting in chronic kidney disease and potential organ failure. There is evidence for a heritable genetic susceptibility to DN, but despite intensive research efforts the causative genes remain elusive. Re...

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Autores principales: Brennan, Eoin, McEvoy, Caitríona, Sadlier, Denise, Godson, Catherine, Martin, Finian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927570/
https://www.ncbi.nlm.nih.gov/pubmed/24705265
http://dx.doi.org/10.3390/genes4040596
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author Brennan, Eoin
McEvoy, Caitríona
Sadlier, Denise
Godson, Catherine
Martin, Finian
author_facet Brennan, Eoin
McEvoy, Caitríona
Sadlier, Denise
Godson, Catherine
Martin, Finian
author_sort Brennan, Eoin
collection PubMed
description Up to 40% of patients with type 1 and type 2 diabetes will develop diabetic nephropathy (DN), resulting in chronic kidney disease and potential organ failure. There is evidence for a heritable genetic susceptibility to DN, but despite intensive research efforts the causative genes remain elusive. Recently, genome-wide association studies have discovered several novel genetic variants associated with DN. The identification of such variants may potentially allow for early identification of at risk patients. Here we review the current understanding of the key molecular mechanisms and genetic architecture of DN, and discuss the merits of employing an integrative approach to incorporate datasets from multiple sources (genetics, transcriptomics, epigenetic, proteomic) in order to fully elucidate the genetic elements contributing to this serious complication of diabetes.
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spelling pubmed-39275702014-03-26 The Genetics of Diabetic Nephropathy Brennan, Eoin McEvoy, Caitríona Sadlier, Denise Godson, Catherine Martin, Finian Genes (Basel) Review Up to 40% of patients with type 1 and type 2 diabetes will develop diabetic nephropathy (DN), resulting in chronic kidney disease and potential organ failure. There is evidence for a heritable genetic susceptibility to DN, but despite intensive research efforts the causative genes remain elusive. Recently, genome-wide association studies have discovered several novel genetic variants associated with DN. The identification of such variants may potentially allow for early identification of at risk patients. Here we review the current understanding of the key molecular mechanisms and genetic architecture of DN, and discuss the merits of employing an integrative approach to incorporate datasets from multiple sources (genetics, transcriptomics, epigenetic, proteomic) in order to fully elucidate the genetic elements contributing to this serious complication of diabetes. MDPI 2013-11-05 /pmc/articles/PMC3927570/ /pubmed/24705265 http://dx.doi.org/10.3390/genes4040596 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Brennan, Eoin
McEvoy, Caitríona
Sadlier, Denise
Godson, Catherine
Martin, Finian
The Genetics of Diabetic Nephropathy
title The Genetics of Diabetic Nephropathy
title_full The Genetics of Diabetic Nephropathy
title_fullStr The Genetics of Diabetic Nephropathy
title_full_unstemmed The Genetics of Diabetic Nephropathy
title_short The Genetics of Diabetic Nephropathy
title_sort genetics of diabetic nephropathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927570/
https://www.ncbi.nlm.nih.gov/pubmed/24705265
http://dx.doi.org/10.3390/genes4040596
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