| Literature DB >> 19430482 |
Anna Köttgen1, Nicole L Glazer, Abbas Dehghan, Shih-Jen Hwang, Ronit Katz, Man Li, Qiong Yang, Vilmundur Gudnason, Lenore J Launer, Tamara B Harris, Albert V Smith, Dan E Arking, Brad C Astor, Eric Boerwinkle, Georg B Ehret, Ingo Ruczinski, Robert B Scharpf, Yii-Der Ida Chen, Ian H de Boer, Talin Haritunians, Thomas Lumley, Mark Sarnak, David Siscovick, Emelia J Benjamin, Daniel Levy, Ashish Upadhyay, Yurii S Aulchenko, Albert Hofman, Fernando Rivadeneira, André G Uitterlinden, Cornelia M van Duijn, Daniel I Chasman, Guillaume Paré, Paul M Ridker, W H Linda Kao, Jacqueline C Witteman, Josef Coresh, Michael G Shlipak, Caroline S Fox.
Abstract
Chronic kidney disease (CKD) has a heritable component and is an important global public health problem because of its high prevalence and morbidity. We conducted genome-wide association studies (GWAS) to identify susceptibility loci for glomerular filtration rate, estimated by serum creatinine (eGFRcrea) and cystatin C (eGFRcys), and CKD (eGFRcrea < 60 ml/min/1.73 m(2)) in European-ancestry participants of four population-based cohorts (ARIC, CHS, FHS, RS; n = 19,877; 2,388 CKD cases), and tested for replication in 21,466 participants (1,932 CKD cases). We identified significant SNP associations (P < 5 × 10(-8)) with CKD at the UMOD locus, with eGFRcrea at UMOD, SHROOM3 and GATM-SPATA5L1, and with eGFRcys at CST and STC1. UMOD encodes the most common protein in human urine, Tamm-Horsfall protein, and rare mutations in UMOD cause mendelian forms of kidney disease. Our findings provide new insights into CKD pathogenesis and underscore the importance of common genetic variants influencing renal function and disease.Entities:
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Year: 2009 PMID： 19430482 PMCID： PMC3039280 DOI： 10.1038/ng.377
Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330