Li Jing, Wu Song, Wang Ming-Rui, Wang Ting-Ting, Li Bai-Kun, Zhu Ji-Min
Department of Public Health and General Medicine, School of Integrated Traditional and Western Medicine, Anhui University of Chinese Medicine, Hefei, Anhui 230038, P.R. China.
Biomed Rep. 2014 Jan;2(1):57-62. doi: 10.3892/br.2013.186. Epub 2013 Oct 23.
Published data on the association between interleukin (IL)-18 gene polymorphisms (-137 C/G, -607 A/C) and type 1 diabetes (T1D) risk are inconclusive. To obtain a more precise estimation of the association between the IL-18 gene polymorphisms and T1D, a meta-analysis was performed. A total of 11 studies including 5,945 cases and 6,404 controls were included in the analysis of the association between -137 C/G and T1D risk. No significant association between -137 C/G and T1D risk was observed in the total population [C vs. G: odds ratio (OR)=1.02, 95% confidence interval (CI)=0.87-1.20; CC + CG vs. GG: OR=1.05, 95% CI=0.87-1.25; CC vs. CG + GG: OR=0.96, 95% CI=0.68-1.36]. No significant association was identified in the stratified analysis for all the genetic models in the European population. Concerning -607 A/C, 10 studies involving 3,048 patients and 3,377 controls were included in this meta-analysis. When all the studies were pooled, the results showed no evidence for a significant association between IL-18 -607 A/C polymorphism and T1D risk (A vs. C: OR=0.93, 95% CI=0.81-1.06; AA + AC vs. CC: OR=0.99, 95% CI=0.89-1.10; AA vs. AC + CC: OR=0.81, 95% CI=0.60-1.09). In addition, similar results were obtained in the subgroup analysis based on ethnicity. In summary, the present meta-analysis suggests a lack of association between the two polymorphisms (-137 C/G, -607 A/C) in the IL-18 gene and T1D. Due to the limitation of the number of the studies, the conclusions drawn should be considered with caution. Larger scale primary studies are required to evaluate the association between IL-18 gene polymorphisms and T1D.
关于白细胞介素(IL)-18基因多态性(-137 C/G、-607 A/C)与1型糖尿病(T1D)风险之间关联的已发表数据尚无定论。为了更精确地评估IL-18基因多态性与T1D之间的关联,进行了一项荟萃分析。在分析-137 C/G与T1D风险的关联时,共纳入了11项研究,包括5945例病例和6404例对照。在总体人群中未观察到-137 C/G与T1D风险之间存在显著关联[C与G比较:比值比(OR)=1.02,95%置信区间(CI)=0.87 - 1.20;CC + CG与GG比较:OR=1.05,95% CI=0.87 - 1.25;CC与CG + GG比较:OR=0.96,95% CI=0.68 - 1.36]。在欧洲人群中对所有遗传模型进行的分层分析中未发现显著关联。关于-607 A/C,该荟萃分析纳入了10项研究,涉及3048例患者和3377例对照。当汇总所有研究时,结果显示没有证据表明IL-18 -607 A/C多态性与T1D风险之间存在显著关联(A与C比较:OR=0.93,95% CI=0.81 - 1.06;AA + AC与CC比较:OR=0.99,95% CI=0.89 - 1.10;AA与AC + CC比较:OR=0.81,95% CI=0.60 - 1.09)。此外,在基于种族的亚组分析中也获得了类似结果。总之,本荟萃分析表明IL-18基因中的两种多态性(-137 C/G、-607 A/C)与T1D之间缺乏关联。由于研究数量有限,得出的结论应谨慎考虑。需要更大规模的初步研究来评估IL-18基因多态性与T1D之间的关联。