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Diabetes. 2009 Dec;58(12):2946-53. doi: 10.2337/db09-0228. Epub 2009 Sep 9.

Additive effects of genetic variation in GCK and G6PC2 on insulin secretion and fasting glucose.

Author information

1
Department of Preventive Medicine, Division of Biostatistics, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Abstract

OBJECTIVE:

Glucokinase (GCK) and glucose-6-phosphatase catalytic subunit 2 (G6PC2) regulate the glucose-cycling step in pancreatic beta-cells and may regulate insulin secretion. GCK rs1799884 and G6PC2 rs560887 have been independently associated with fasting glucose, but their interaction on glucose-insulin relationships is not well characterized.

RESEARCH DESIGN AND METHODS:

We tested whether these variants are associated with diabetes-related quantitative traits in Mexican Americans from the BetaGene Study and attempted to replicate our findings in Finnish men from the METabolic Syndrome in Men (METSIM) Study.

RESULTS:

rs1799884 was not associated with any quantitative trait (corrected P > 0.1), whereas rs560887 was significantly associated with the oral glucose tolerance test 30-min incremental insulin response (30' Deltainsulin, corrected P = 0.021). We found no association between quantitative traits and the multiplicative interaction between rs1799884 and rs560887 (P > 0.26). However, the additive effect of these single nucleotide polymorphisms was associated with fasting glucose (corrected P = 0.03) and 30' Deltainsulin (corrected P = 0.027). This additive association was replicated in METSIM (fasting glucose, P = 3.5 x 10(-10) 30' Deltainsulin, P = 0.028). When we examined the relationship between fasting glucose and 30' Deltainsulin stratified by GCK and G6PC2, we noted divergent changes in these quantitative traits for GCK but parallel changes for G6PC2. We observed a similar pattern in METSIM.

CONCLUSIONS:

Our data suggest that variation in GCK and G6PC2 have additive effects on both fasting glucose and insulin secretion.

PMID:
19741163
PMCID:
PMC2780888
DOI:
10.2337/db09-0228
[Indexed for MEDLINE]
Free PMC Article

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