Kim J H, Shin H D, Park B L, Cho Y M, Kim S Y, Lee H K, Park K S
Department of Internal Medicine, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Gu, Seoul, 110-744, South Korea.
Diabetologia. 2005 Jul;48(7):1323-30. doi: 10.1007/s00125-005-1793-4. Epub 2005 Jun 4.
AIMS/HYPOTHESIS: Peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1alpha) is a transcriptional coactivator implicated in insulin release by beta cells and in insulin resistance. Therefore, genetic variation of PPARGC1A could be implicated in the onset of type 2 diabetes. In this study, we examined whether the PPARGC1A gene locus is associated with type 2 diabetes mellitus. We also investigated its association with clinical and metabolic parameters in healthy and diabetic subjects.
After sequencing exons and their boundaries of the PPARGC1A gene, including the promoter region ( approximately 1.5 kb), we genotyped eight common single nucleotide polymorphisms (SNPs) in an association study comprising 762 unrelated patients with type 2 diabetes and 303 non-diabetic control patients. We divided the patients with type 2 diabetes into quartiles or three groups according to age at diagnosis of type 2 diabetes (early-onset: <40 years of age, average-onset: 40< or = <60 years, and late-onset: > or =60 years).
There was no strong association between SNPs or haplotypes of PPARGC1A and type 2 diabetes. However, the SNPs of g.-1789G>A and g.-1437C>T were associated with the age at diagnosis of type 2 diabetes (p=0.042 and p=0.032, respectively). In addition, the promoter SNPs of g.-1789G>A and g.-1437C>T and the haplotypes ht2 (-1789A and -1437T) were significantly associated with early-onset type 2 diabetes (p=0.002, p=0.001 and p=0.001, respectively).
CONCLUSIONS/INTERPRETATION: Our results suggest that PPARGC1A promoter polymorphisms are associated with age at diagnosis of type 2 diabetes and early-onset type 2 diabetes in the Korean population.
目的/假设:过氧化物酶体增殖物激活受体γ辅激活因子1α(PGC-1α)是一种转录辅激活因子,与β细胞的胰岛素分泌及胰岛素抵抗有关。因此,PPARGC1A的基因变异可能与2型糖尿病的发病有关。在本研究中,我们检测了PPARGC1A基因位点是否与2型糖尿病相关。我们还研究了其与健康受试者和糖尿病患者的临床及代谢参数之间的关联。
在对PPARGC1A基因的外显子及其边界(包括启动子区域,约1.5 kb)进行测序后,我们在一项关联研究中对8个常见单核苷酸多态性(SNP)进行了基因分型,该研究包括762例无亲缘关系的2型糖尿病患者和303例非糖尿病对照患者。我们根据2型糖尿病诊断时的年龄将2型糖尿病患者分为四分位数或三组(早发型:<40岁,平均发病年龄:40≤<60岁,晚发型:≥60岁)。
PPARGC1A的SNP或单倍型与2型糖尿病之间无强关联。然而,g.-1789G>A和g.-1437C>T的SNP与2型糖尿病诊断时的年龄相关(分别为p=0.042和p=0.032)。此外,g.-1789G>A和g.-1437C>T的启动子SNP以及单倍型ht2(-1789A和-1437T)与早发型2型糖尿病显著相关(分别为p=0.002、p=0.001和p=0.001)。
结论/解读:我们的结果表明,在韩国人群中,PPARGC1A启动子多态性与2型糖尿病诊断时的年龄及早发型2型糖尿病相关。