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000180331 005__ 20240229145614.0
000180331 0247_ $$2doi$$a10.1038/s42003-022-03448-z
000180331 0247_ $$2pmid$$apmid:35697829
000180331 0247_ $$2altmetric$$aaltmetric:129654651
000180331 037__ $$aDKFZ-2022-01258
000180331 041__ $$aEnglish
000180331 082__ $$a570
000180331 1001_ $$00000-0003-0292-5421$$aWinkler, Thomas W$$b0
000180331 245__ $$aDifferential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
000180331 260__ $$aLondon$$bSpringer Nature$$c2022
000180331 3367_ $$2DRIVER$$aarticle
000180331 3367_ $$2DataCite$$aOutput Types/Journal article
000180331 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1655211030_12408
000180331 3367_ $$2BibTeX$$aARTICLE
000180331 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000180331 3367_ $$00$$2EndNote$$aJournal Article
000180331 520__ $$aReduced glomerular filtration rate (GFR) can progress to kidney failure. Risk factors include genetics and diabetes mellitus (DM), but little is known about their interaction. We conducted genome-wide association meta-analyses for estimated GFR based on serum creatinine (eGFR), separately for individuals with or without DM (nDM = 178,691, nnoDM = 1,296,113). Our genome-wide searches identified (i) seven eGFR loci with significant DM/noDM-difference, (ii) four additional novel loci with suggestive difference and (iii) 28 further novel loci (including CUBN) by allowing for potential difference. GWAS on eGFR among DM individuals identified 2 known and 27 potentially responsible loci for diabetic kidney disease. Gene prioritization highlighted 18 genes that may inform reno-protective drug development. We highlight the existence of DM-only and noDM-only effects, which can inform about the target group, if respective genes are advanced as drug targets. Largely shared effects suggest that most drug interventions to alter eGFR should be effective in DM and noDM.
000180331 536__ $$0G:(DE-HGF)POF4-313$$a313 - Krebsrisikofaktoren und Prävention (POF4-313)$$cPOF4-313$$fPOF IV$$x0
000180331 588__ $$aDataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
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000180331 7001_ $$astudy, Lifelines cohort$$b306$$eCollaboration Author
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000180331 7001_ $$aProgram, VA Million Veteran$$b308$$eCollaboration Author
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