Journal
JOURNAL OF HUMAN GENETICS
Volume 48, Issue 12, Pages 614-621Publisher
NATURE PUBLISHING GROUP
DOI: 10.1007/s10038-003-0087-2
Keywords
peroxisome proliferator-activated receptors; OGTT; epistasis; type 2 diabetes; C-peptide; insulin homeostasis; PPAR(gamma 2); P12A mutation; PPAR alpha; L162V mutation
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Peroxisome proliferator-activated receptors gamma(2) and alpha are nuclear factors known to be important regulators of lipid and glucose metabolism. Two polymorphisms, namely PPARgamma(2) P12A and PPARalpha L162V, were investigated for their individual and interaction effects on glucose and insulin homeostasis. Genotypes were determined in 663 nondiabetic adults participating in the Quebec Family Study and who underwent an oral glucose tolerance test (OGTT). The insulin and C-peptide areas under the curve (AUC) following the OGTT were higher in subjects carrying the PPARalpha V162 allele compared to homozygous for the L162 allele. When subjects were grouped according to both polymorphisms, higher levels of insulin and C-peptide during the OGTT were observed for those carrying the PPARalpha V162 allele except when they carry at the same time the PPARgamma(2) A12 allele. Thus, the PPARgamma(2) A12 allele seems protective against the deleterious effect of the PPARalpha V162 allele. Furthermore, a significant gene-gene interaction was observed for the acute (0-30 min) (p<0.001) and the total (p=0.05) C-peptide AUC following the OGTT. These results provide evidence of a gene-gene interaction in the regulation of plasma glucose-insulin homeostasis, and emphasize that these interactions need to be taken into account when dissecting the genetic etiology of complex disorders.
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