A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Pattaro, Cristian and De Grandi, Alessandro and Vitart, Veronique and Hayward, Caroline and Franke, Andre and Aulchenko, Yurii S. and Johansson, Asa and Wild, Sarah H. and Melville, Scott A. and Isaacs, Aaron and Polasek, Ozren and Ellinghaus, David and Kolcic, Ivana and Noethlings, Ute and Zgaga, Lina and Zemunik, Tatijana and Gnewuch, Carsten and Schreiber, Stefan and Campbell, Susan and Hastie, Nick and Boban, Mladen and Meitinger, Thomas and Oostra, Ben A. and Riegler, Peter and Minelli, Cosetta and Wright, Alan F. and Campbell, Harry and van Duijn, Cornelia M. and Gyllensten, Ulf and Wilson, James F. and Krawczak, Michael and Rudan, Igor and Pramstaller, Peter P. (2010) A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. BMC MEDICAL GENETICS, 11: 41. ISSN 1471-2350,

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Abstract

Background: Serum creatinine (S-CR) is the most important biomarker for a quick and non-invasive assessment of kidney function in population-based surveys. A substantial proportion of the inter-individual variability in SCR level is explicable by genetic factors. Methods: We performed a meta-analysis of genome-wide association studies of SCR undertaken in five population isolates ('discovery cohorts'), all of which are part of the European Special Population Network (EUROSPAN) project. Genes showing the strongest evidence for an association with SCR (candidate loci) were replicated in two additional population-based samples ('replication cohorts'). Results: After the discovery meta-analysis, 29 loci were selected for replication. Association between SCR level and polymorphisms in the collagen type XXII alpha 1 (COL22A1) gene, on chromosome 8, and in the synaptotagmin-1 (SYT1) gene, on chromosome 12, were successfully replicated in the replication cohorts (p value = 1.0 x 10(-6) and 1.7 x 10(-4), respectively). Evidence of association was also found for polymorphisms in a locus including the gamma-aminobutyric acid receptor rho-2 (GABRR2) gene and the ubiquitin-conjugating enzyme E2-J1 (UBE2J1) gene (replication p value = 3.6 x 10(-3)). Previously reported findings, associating glomerular filtration rate with SNPs in the uromodulin (UMOD) gene and in the schroom family member 3 (SCHROOM3) gene were also replicated. Conclusions: While confirming earlier results, our study provides new insights in the understanding of the genetic basis of serum creatinine regulatory processes. In particular, the association with the genes SYT1 and GABRR2 corroborate previous findings that highlighted a possible role of the neurotransmitters GABA(A) receptors in the regulation of the glomerular basement membrane and a possible interaction between GABA(A)receptors and synaptotagmin-I at the podocyte level.

Item Type: Article
Uncontrolled Keywords: GLOMERULAR-FILTRATION-RATE; CHRONIC KIDNEY-DISEASE; STAGE RENAL-DISEASE; LINKAGE DISEQUILIBRIUM; ISOLATED POPULATION; AFRICAN-AMERICANS; FRAMINGHAM HEART; SOUTH TYROL; TRAITS; ISLAND;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin
Depositing User: Dr. Gernot Deinzer
Date Deposited: 05 Aug 2020 04:35
Last Modified: 05 Aug 2020 04:35
URI: https://pred.uni-regensburg.de/id/eprint/24977

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