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Metabolic syndrome(MetS) and type 2 diabetes mellitus(T2DM) are the serious public health problems worldwide.Moreover,it is estimated that MetS patients have about five-fold greater risk of the T2 DM development compared with people without the syndrome.Peroxisome proliferator-activated receptors are a subgroup of the nuclear hormone receptor superfamily of ligand-activated transcription factors which play an important role in the pathogenesis of MetS and T2 DM.All three members of the peroxisome proliferator-activated receptor(PPAR) nuclear receptor subfamily,PPARα,PPARp/5 and PPARγ are critical in regulating insulin sensitivity,adipogenesis,lipid metabolism,and blood pressure.Recently,more and more studies indicated that the gene polymorphism of PPARs,such as Leu~(162)Val and Val~(227)Ala of PPARα,+294T> C of PPARβ/δ,Pro~(12)Ala and C1431 T of PPARγ,are significantly associated with the onset and progressing of MetS and T2 DM in different population worldwide.Furthermore,a large body of evidence demonstrated that the glucose metabolism and lipid metabolism were influenced by gene-gene interaction among PPARs genes.However,given the complexity pathogenesis of metabolic disease,it is unlikely that genetic variation of a single locus would provide an adequate explanation of inter-individual differences which results in diverse clinical syndromes.Thus,gene-gene interactions and gene-environment interactions associated with T2 DM and MetS need future comprehensive studies.
Metabolic syndrome (MetS) and type 2 diabetes mellitus (T2DM) are the serious public health problems worldwide. Moreover, it is estimated that MetS patients have about five-fold greater risk of the T2 DM development compared with people without the syndrome. Peroxisome proliferator -activated receptors are a subgroup of the nuclear hormone receptor superfamily of ligand-activated transcription factors which play an important role in the pathogenesis of MetS and T2 DM. All three members of the peroxisome proliferator-activated receptor (PPAR) nuclear receptor subfamily, PPAR [alpha] , PPARp / 5 and PPARγ are critical in regulating insulin sensitivity, adipogenesis, lipid metabolism, and blood pressure. Recently, more and more studies indicate that the gene polymorphism of PPARs, such as Leu ~ (162) Val and Val ~ Ala of PPARα, + 294T> C of PPARβ / δ, Pro ~ (12) Ala and C1431 T of PPARγ, are significantly associated with the onset and progressing of MetS and T2 DM in different population worldwide. Frthermore, a larg e body of evidence demonstrated the the glucose metabolism and lipid metabolism were influenced by gene-gene interaction among PPARs genes. Yetever, given the complex pathogenesis of metabolic disease, it is unlikely that genetic variation of a single locus would provide an adequate explanation of inter -individual differences which results in diverse clinical syndromes. Thus, gene-gene interactions and gene-environment interactions associated with T2 DM and MetS need future comprehensive studies.