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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genes 2013-11, Vol.4 (4), p.596-619
Hauptverfasser: Brennan, Eoin, McEvoy, Caitríona, Sadlier, Denise, Godson, Catherine, Martin, Finian
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 619
container_issue 4
container_start_page 596
container_title Genes
container_volume 4
creator Brennan, Eoin
McEvoy, Caitríona
Sadlier, Denise
Godson, Catherine
Martin, Finian
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.
doi_str_mv 10.3390/genes4040596
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3927570</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1514436788</sourcerecordid><originalsourceid>FETCH-LOGICAL-c412t-2c259041ab79baa8505ef80c76dab1f8849a286e8ecfbe9c0555545cb4bab7303</originalsourceid><addsrcrecordid>eNpdkUtLw0AQxxdRbKm9eZaAHjwYnX0luxdBii8oeKnnZXe7aVLSbMwmQr-9Ca2lOpeZYX7zZx4IXWK4p1TCw8pVLjBgwGVygsYEUhozRvjpUTxC0xDW0BsDAsDP0YiwFDhJ-BjdLHIXDSptYUPks2hZaDMkUeXqvPG1bvPtBTrLdBncdO8n6PPleTF7i-cfr--zp3lsGSZtTCzhEhjWJpVGa8GBu0yATZOlNjgTgklNROKEs5lx0gLvjXFrmOlbKNAJetzp1p3ZuKV1VdvoUtVNsdHNVnldqL-VqsjVyn8rKknK00Hgdi_Q-K_OhVZtimBdWerK-S4ozDFjNEmF6NHrf-jad03Vr9dThEmMhwNO0N2Oso0PoXHZYRgMaviAOv5Aj18dL3CAf-9NfwDEMYDO</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1524911207</pqid></control><display><type>article</type><title>The genetics of diabetic nephropathy</title><source>PubMed Central Open Access</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Brennan, Eoin ; McEvoy, Caitríona ; Sadlier, Denise ; Godson, Catherine ; Martin, Finian</creator><creatorcontrib>Brennan, Eoin ; McEvoy, Caitríona ; Sadlier, Denise ; Godson, Catherine ; Martin, Finian</creatorcontrib><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.</description><identifier>ISSN: 2073-4425</identifier><identifier>EISSN: 2073-4425</identifier><identifier>DOI: 10.3390/genes4040596</identifier><identifier>PMID: 24705265</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Genetics ; Review</subject><ispartof>Genes, 2013-11, Vol.4 (4), p.596-619</ispartof><rights>Copyright MDPI AG 2013</rights><rights>2013 by the authors; licensee MDPI, Basel, Switzerland. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-2c259041ab79baa8505ef80c76dab1f8849a286e8ecfbe9c0555545cb4bab7303</citedby><cites>FETCH-LOGICAL-c412t-2c259041ab79baa8505ef80c76dab1f8849a286e8ecfbe9c0555545cb4bab7303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927570/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927570/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,313,314,727,780,784,792,885,27920,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24705265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brennan, Eoin</creatorcontrib><creatorcontrib>McEvoy, Caitríona</creatorcontrib><creatorcontrib>Sadlier, Denise</creatorcontrib><creatorcontrib>Godson, Catherine</creatorcontrib><creatorcontrib>Martin, Finian</creatorcontrib><title>The genetics of diabetic nephropathy</title><title>Genes</title><addtitle>Genes (Basel)</addtitle><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.</description><subject>Genetics</subject><subject>Review</subject><issn>2073-4425</issn><issn>2073-4425</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkUtLw0AQxxdRbKm9eZaAHjwYnX0luxdBii8oeKnnZXe7aVLSbMwmQr-9Ca2lOpeZYX7zZx4IXWK4p1TCw8pVLjBgwGVygsYEUhozRvjpUTxC0xDW0BsDAsDP0YiwFDhJ-BjdLHIXDSptYUPks2hZaDMkUeXqvPG1bvPtBTrLdBncdO8n6PPleTF7i-cfr--zp3lsGSZtTCzhEhjWJpVGa8GBu0yATZOlNjgTgklNROKEs5lx0gLvjXFrmOlbKNAJetzp1p3ZuKV1VdvoUtVNsdHNVnldqL-VqsjVyn8rKknK00Hgdi_Q-K_OhVZtimBdWerK-S4ozDFjNEmF6NHrf-jad03Vr9dThEmMhwNO0N2Oso0PoXHZYRgMaviAOv5Aj18dL3CAf-9NfwDEMYDO</recordid><startdate>20131105</startdate><enddate>20131105</enddate><creator>Brennan, Eoin</creator><creator>McEvoy, Caitríona</creator><creator>Sadlier, Denise</creator><creator>Godson, Catherine</creator><creator>Martin, Finian</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20131105</creationdate><title>The genetics of diabetic nephropathy</title><author>Brennan, Eoin ; McEvoy, Caitríona ; Sadlier, Denise ; Godson, Catherine ; Martin, Finian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-2c259041ab79baa8505ef80c76dab1f8849a286e8ecfbe9c0555545cb4bab7303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Genetics</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brennan, Eoin</creatorcontrib><creatorcontrib>McEvoy, Caitríona</creatorcontrib><creatorcontrib>Sadlier, Denise</creatorcontrib><creatorcontrib>Godson, Catherine</creatorcontrib><creatorcontrib>Martin, Finian</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brennan, Eoin</au><au>McEvoy, Caitríona</au><au>Sadlier, Denise</au><au>Godson, Catherine</au><au>Martin, Finian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The genetics of diabetic nephropathy</atitle><jtitle>Genes</jtitle><addtitle>Genes (Basel)</addtitle><date>2013-11-05</date><risdate>2013</risdate><volume>4</volume><issue>4</issue><spage>596</spage><epage>619</epage><pages>596-619</pages><issn>2073-4425</issn><eissn>2073-4425</eissn><abstract>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.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>24705265</pmid><doi>10.3390/genes4040596</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2073-4425
ispartof Genes, 2013-11, Vol.4 (4), p.596-619
issn 2073-4425
2073-4425
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3927570
source PubMed Central Open Access; MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Genetics
Review
title The genetics of diabetic nephropathy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T23%3A22%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20genetics%20of%20diabetic%20nephropathy&rft.jtitle=Genes&rft.au=Brennan,%20Eoin&rft.date=2013-11-05&rft.volume=4&rft.issue=4&rft.spage=596&rft.epage=619&rft.pages=596-619&rft.issn=2073-4425&rft.eissn=2073-4425&rft_id=info:doi/10.3390/genes4040596&rft_dat=%3Cproquest_pubme%3E1514436788%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1524911207&rft_id=info:pmid/24705265&rfr_iscdi=true