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Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function
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2012 (English)In: PLoS Genetics, ISSN 1553-7390, Vol. 8, no 3, e1002584- p.Article in journal (Refereed) Published
Abstract [en]

Chronic kidney disease (CKD) is an important public health problem with a genetic component. We performed genomewide association studies in up to 130,600 European ancestry participants overall, and stratified for key CKD risk factors. We uncovered 6 new loci in association with estimated glomerular filtration rate (eGFR), the primary clinical measure of CKD, in or near MPPED2, DDX1, SLC47A1, CDK12, CASP9, and INO80. Morpholino knockdown of mpped2 and casp9 in zebrafish embryos revealed podocyte and tubular abnormalities with altered dextran clearance, suggesting a role for these genes in renal function. By providing new insights into genes that regulate renal function, these results could further our understanding of the pathogenesis of CKD.

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2012. Vol. 8, no 3, e1002584- p.
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Medical Genetics
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URN: urn:nbn:se:uu:diva-174593DOI: 10.1371/journal.pgen.1002584ISI: 000302254800059OAI: oai:DiVA.org:uu-174593DiVA: diva2:529175
Available from: 2012-05-29 Created: 2012-05-22 Last updated: 2018-01-12Bibliographically approved

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Johansson, ÅsaGyllensten, Ulf
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GenomicsDepartment of Immunology, Genetics and Pathology
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CiteExportLink to record
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