Department of Pharmacy, Jurong Hospital affiliated to Jiangsu University, Jurong 212400, Jiangsu, China.
Zhenjiang First People's Hospital, Zhenjiang 212000, Jiangsu, China.
Biosci Rep. 2018 Dec 7;38(6). doi: 10.1042/BSR20181275. Print 2018 Dec 21.
: Urotensin-II (UII) rs228648 polymorphism has been reported to be associated with the risk of diabetes mellitus (DM) with inconsistent results. The present study sought to reassess the relationship between this polymorphism and susceptibility to DM by meta-analysis.: Relevant eligible studies and whole genome association study (GWAS) data electronically searched were pooled to evaluate the strength of the association with odds ratios (ORs) and 95% confidence intervals (CIs).: Seven case-control studies involving 894 cases and 1186 controls were finally included in the meta-analysis. Overall analyses indicated that UII gene rs228648 variant was significantly associated with reduced risk of DM (allele, A vs. G: OR = 0.68, 95%CI = 0.56-0.82; dominant, AA+GA vs. GG: OR = 0.70, 95%CI = 0.53-0.91; homozygote, AA vs. GG: OR = 0.41, 95%CI = 0.28-0.61; recessive, AA vs. GA+GG: OR = 0.36, 95%CI = 0.19-0.71). In subgroup analyses based on ethnicity, the results showed a significant association of rs228648 polymorphism with decreased risk of DM in Chinese population under all five genetic models as well as in non-Chinese population under heterozygote and recessive models. Stratified analyses by specific type of DM also presented a significant association for common diabetes mellitus (CDM) under allele and homozygote as well as gestational diabetes mellitus (GDM) under all genetic models except for homozygote model. However, the synthetic analysis with GWAS data suggested an increased risk of DM with rs228648 effect allele in European population (OR = 1.01, 95%CI = 1.00-1.02).: The present meta-analysis preliminarily suggested a potentially opposite role of rs228648 polymorphism associated with DM risk in the Chinese and European population. Further studies are in great request to verify the results.
: 尿皮质素-II (UII) rs228648 多态性与糖尿病 (DM) 风险相关,但结果不一致。本研究通过荟萃分析重新评估了这种多态性与 DM 易感性之间的关系。: 电子检索了相关的合格研究和全基因组关联研究 (GWAS) 数据,以评估优势比 (OR) 和 95%置信区间 (CI) 的关联强度。: 最终纳入了 7 项病例对照研究,共 894 例病例和 1186 例对照。总体分析表明,UII 基因 rs228648 变异与 DM 风险降低显著相关(等位基因,A 对 G:OR = 0.68,95%CI = 0.56-0.82;显性,AA+GA 对 GG:OR = 0.70,95%CI = 0.53-0.91;纯合子,AA 对 GG:OR = 0.41,95%CI = 0.28-0.61;隐性,AA 对 GA+GG:OR = 0.36,95%CI = 0.19-0.71)。基于种族的亚组分析结果显示,在所有五种遗传模型下,rs228648 多态性与中国人群 DM 风险降低显著相关,在非中国人群杂合子和隐性模型下也显著相关。按特定类型的 DM 进行的分层分析显示,在所有遗传模型下,除纯合子模型外,常见糖尿病 (CDM) 的等位基因和纯合子模型以及妊娠糖尿病 (GDM) 的所有遗传模型下,rs228648 多态性与风险降低显著相关。然而,与 GWAS 数据的综合分析表明,在欧洲人群中,rs228648 效应等位基因增加了 DM 的风险(OR = 1.01,95%CI = 1.00-1.02)。: 本荟萃分析初步提示 rs228648 多态性与中国和欧洲人群 DM 风险相关的潜在相反作用。需要进一步的研究来验证这些结果。