Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.


Chen, WM; Erdos, MR; Jackson, AU; Saxena, R; Sanna, S; Silver, KD; Timpson, NJ; Hansen, T; Orrù, M; Grazia Piras, M; Bonnycastle, LL; Willer, CJ; Lyssenko, V; Shen, H; Kuusisto, J; Ebrahim, S; Sestu, N; Duren, WL; Spada, MC; Stringham, HM; Scott, LJ; Olla, N; Swift, AJ; Najjar, S; Mitchell, BD; Lawlor, DA; Smith, GD; Ben-Shlomo, Y; Andersen, G; Borch-Johnsen, K; Jørgensen, T; Saramies, J; Valle, TT; Buchanan, TA; Shuldiner, AR; Lakatta, E; Bergman, RN; Uda, M; Tuomilehto, J; Pedersen, O; Cao, A; Groop, L; Mohlke, KL; Laakso, M; Schlessinger, D; Collins, FS; Altshuler, D; Abecasis, GR; Boehnke, M; Scuteri, A; Watanabe, RM; (2008) Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. The Journal of clinical investigation, 118 (7). pp. 2620-8. ISSN 0021-9738 DOI: 10.1172/JCI34566

Full text not available from this repository.

Abstract

Identifying the genetic variants that regulate fasting glucose concentrations may further our understanding of the pathogenesis of diabetes. We therefore investigated the association of fasting glucose levels with SNPs in 2 genome-wide scans including a total of 5,088 nondiabetic individuals from Finland and Sardinia. We found a significant association between the SNP rs563694 and fasting glucose concentrations (P = 3.5 x 10(-7)). This association was further investigated in an additional 18,436 nondiabetic individuals of mixed European descent from 7 different studies. The combined P value for association in these follow-up samples was 6.9 x 10(-26), and combining results from all studies resulted in an overall P value for association of 6.4 x 10(-33). Across these studies, fasting glucose concentrations increased 0.01-0.16 mM with each copy of the major allele, accounting for approximately 1% of the total variation in fasting glucose. The rs563694 SNP is located between the genes glucose-6-phosphatase catalytic subunit 2 (G6PC2) and ATP-binding cassette, subfamily B (MDR/TAP), member 11 (ABCB11). Our results in combination with data reported in the literature suggest that G6PC2, a glucose-6-phosphatase almost exclusively expressed in pancreatic islet cells, may underlie variation in fasting glucose, though it is possible that ABCB11, which is expressed primarily in liver, may also contribute to such variation.

Item Type: Article
Faculty and Department: Faculty of Epidemiology and Population Health > Dept of Non-Communicable Disease Epidemiology
Research Centre: Centre for Global Non-Communicable Diseases (NCDs)
PubMed ID: 18521185
Web of Science ID: 257657400029
URI: http://researchonline.lshtm.ac.uk/id/eprint/7542

Statistics


Download activity - last 12 months
Downloads since deposit
0Downloads
273Hits
Accesses by country - last 12 months
Accesses by referrer - last 12 months
Impact and interest
Additional statistics for this record are available via IRStats2

Actions (login required)

Edit Item Edit Item