Du Fei, Yang Kang-Juan, Piao Lian-Shan
Department of Cell Biology and Medical Genetics, Yanbian University Medical College, Yanji, Jilin,133000, China.
Department of Endocrinology, Affiliated Hospital of Yanbian University, Yanji, Jilin,133000, China.
Open Life Sci. 2019 May 21;14:43-52. doi: 10.1515/biol-2019-0006. eCollection 2019 Jan.
To systematically investigate the correlation between the G>A polymorphism of the peroxisome proliferator-activated receptor γ coactivator 1α () gene rs8192678 locus and the susceptibility to type-2 diabetes mellitus (T2DM).
The inclusion and exclusion criteria and retrieval strategies of original literatures were formulated. Then, subjects and free words "PPARGC1A","gene polymorphism", and "T2DM" were retrieved from the PubMed, EMBASE, and Cochrane Library databases. Case-control studies on the G>A polymorphism of the gene rs8192678 locus and susceptibility to T2DM were included for the meta-analysis.
The number of cases in the T2DM group and control group was 5,607 and 7,596, respectively. The meta-analysis revealed that the gene rs8192678 locus G>A polymorphism is associated with susceptibility to T2DM. There are differences in each group of genetic models, of which three groups of genetic models are highly significant. In the allele model, OR=1.249, 95% CI: 1.099-1.419, and =0.001. In the dominant inheritance model, OR=1.364, 95% CI: 1.152-1.614, and =0.000. In the additive inheritance model, OR=0.828, 95% CI: 0.726-0.945, and =0.005. And one group is significant, in the recessive inheritance model, OR=1.187, 95% CI: 1.021-1.381, and =0.026.
In Western Asian, South Asian, European and African populations, the A allele of the gene rs8192678 locus may be one of the risk factors for T2DM.
系统研究过氧化物酶体增殖物激活受体γ共激活因子1α(PPARGC1A)基因rs8192678位点G>A多态性与2型糖尿病(T2DM)易感性之间的相关性。
制定原始文献的纳入和排除标准以及检索策略。然后,从PubMed、EMBASE和Cochrane图书馆数据库中检索以“PPARGC1A”“基因多态性”和“T2DM”为主题词和自由词的文献。纳入关于PPARGC1A基因rs8192678位点G>A多态性与T2DM易感性的病例对照研究进行荟萃分析。
T2DM组和对照组的病例数分别为5607例和7596例。荟萃分析显示,PPARGC1A基因rs8192678位点G>A多态性与T2DM易感性相关。各遗传模型组存在差异,其中三组遗传模型差异高度显著。在等位基因模型中,OR=1.249,95%CI:1.099-1.419,P=0.001。在显性遗传模型中,OR=1.364,95%CI:1.152-1.614,P=0.000。在加性遗传模型中,OR=0.828,95%CI:0.726-0.945,P=0.005。还有一组差异显著,在隐性遗传模型中,OR=1.187,95%CI:1.021-1.381,P=0.026。
在西亚、南亚、欧洲和非洲人群中,PPARGC1A基因rs8192678位点的A等位基因可能是T2DM的危险因素之一。