001     180331
005     20240229145614.0
024 7 _ |a 10.1038/s42003-022-03448-z
|2 doi
024 7 _ |a pmid:35697829
|2 pmid
024 7 _ |a altmetric:129654651
|2 altmetric
037 _ _ |a DKFZ-2022-01258
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Winkler, Thomas W
|0 0000-0003-0292-5421
|b 0
245 _ _ |a Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
260 _ _ |a London
|c 2022
|b Springer Nature
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1655211030_12408
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
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520 _ _ |a Reduced 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.
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700 1 _ |a Milaneschi, Yuri
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700 1 _ |a Yu, Zhi
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700 1 _ |a study, Lifelines cohort
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|e Collaboration Author
700 1 _ |a study, DiscovEHR/MyCode
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|e Collaboration Author
700 1 _ |a Program, VA Million Veteran
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|e Collaboration Author
700 1 _ |a Stark, Klaus J
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700 1 _ |a Stefansson, Kari
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700 1 _ |a Böger, Carsten A
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700 1 _ |a Pattaro, Cristian
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700 1 _ |a Heid, Iris M
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700 1 _ |a Thio, Chris H L
|b 317
700 1 _ |a van der Most, Peter J
|b 318
700 1 _ |a de Borst, Martin H
|b 319
700 1 _ |a Ho, Kevin
|b 320
700 1 _ |a Josyula, Navya Shilpa
|b 321
700 1 _ |a Pendergrass, Sarah A
|b 322
700 1 _ |a Rowan, Bryce X
|b 323
700 1 _ |a Robinson-Cohen, Cassianne
|b 324
700 1 _ |a Gaziano, John M
|b 325
700 1 _ |a Phillips, Lawrence S
|b 326
700 1 _ |a Tao, Ran
|b 327
700 1 _ |a Hung, Adriana M
|b 328
773 _ _ |a 10.1038/s42003-022-03448-z
|g Vol. 5, no. 1, p. 580
|0 PERI:(DE-600)2919698-X
|n 1
|p 580
|t Communications biology
|v 5
|y 2022
|x 2399-3642
909 C O |o oai:inrepo02.dkfz.de:180331
|p VDB
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