Association of PON2 Gene Polymorphisms (Ser311Cys and Ala148Gly) With the Risk of Developing Type 2 Diabetes Mellitus in the Chinese Population.
Association of PON2 Gene Polymorphisms (Ser311Cys and Ala148Gly) With the Risk of Developing Type 2 Diabetes Mellitus in the Chinese Population.
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PON2 基因多态性(Ser311Cys 和 Ala148Gly)与中国人群患 2 型糖尿病风险的关联
DOI:
10.3389/fendo.2018.00495
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发表时间:
2018
影响因子:
5.2
通讯作者:
Luo JQ
中科院分区:
文献类型:
--
作者:
Ren H;Tan SL;Liu MZ;Banh HL;Luo JQ
Background: The association between paraoxonase 2 (PON2) gene polymorphisms and type 2 diabetes mellitus (T2DM) has been extensively investigated in the Chinese population with conflicting results. In this study, we systematically evaluated the association between PON2 Ser311Cys and Ala148Gly polymorphisms and T2DM risk by pooling all relevant studies. Methods: We searched PubMed, Embase, CNKI, and Wanfang databases for the studies. The strength of association was determined by the allelic, homozygous, heterozygous, recessive, and dominant genetic models and measured as odds ratio (OR) and 95% confidence interval (CI), under fixed- or random-effect models. Results: There was no significant association between PON2 Ser311Cys polymorphism and T2DM under any of the genetic models: allelic (OR = 1.06, 95% CI = 0.77–1.45; P = 0.721), heterozygous (OR = 1.13, 95% CI = 0.87–1.45; P = 0.362), dominant (OR = 1.10, 95% CI = 0.80–1.51; P = 0.562), recessive (OR = 0.87, 95% CI = 0.48–1.58; P = 0.648), homozygous (OR = 0.94, 95% CI = 0.47–1.89; P = 0.865). Similarly, no significant association was found in PON2 Arg148Gly polymorphism under any of the models: allelic (OR = 1.17, 95% CI = 0.91–1.50; P = 0.218), heterozygous (OR = 1.28, 95% CI = 0.94–1.74; P = 0.117), dominant (OR = 1.25, 95% CI = 0.93–1.67; P = 0.142), recessive (OR = 0.99, 95% CI = 0.52–1.88; P = 0.973), homozygous (OR = 1.08, 95% CI = 0.57–2.07; P = 0.808). Conclusions: The PON2 Ser311Cys and Ala148Gly polymorphisms were not associated with the risk of developing T2DM in the Chinese population.
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影响因子:
3
作者:
Li S;Xiao J;Ji L;Weng J;Jia W;Lu J;Zhou Z;Guo X;Liu J;Shan Z;Zhu D;Chen L;Zhao Z;Tian H;Ji Q;Ge J;Li Q;Lin L;Yang Z;He J;Yang W;China National Diabetes and Metabolic Disorders Study Investigators
通讯作者:
China National Diabetes and Metabolic Disorders Study Investigators
影响因子:
5.3
作者:
Luo JQ;Ren H;Liu MZ;Fang PF;Xiang DX
通讯作者:
Xiang DX
影响因子:
4.8
作者:
Ng, CJ;Wadleigh, DJ;Reddy, ST
通讯作者:
Reddy, ST
影响因子:
5.8
作者:
Hegele, RA;Connelly, PW;Zinman, B
通讯作者:
Zinman, B
影响因子:
105.7
作者:
Higgins, JPT;Thompson, SG;Altman, DG
通讯作者:
Altman, DG