Areeshi Mohammed Y, Mandal Raju K, Dar Sajad A, Alshahrani Abdulrahman M, Ahmad Aqeel, Jawed Arshad, Wahid Mohd, Lohani Mohtashim, Panda Aditya K, Haque Shafiul
Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan 45142, Saudi Arabia.
Department of Microbiology, University College of Medical Sciences and GTB Hospital (University of Delhi), Delhi 110095, India.
Biosci Rep. 2017 Jun 8;37(3). doi: 10.1042/BSR20170247. Print 2017 Jun 30.
I (rs1544410) polymorphism located in intron 8 at the 3'-end of the vitamin D receptor (VDR) gene is known to be involved in the regulation of mRNA stability. Many studies evaluated the possible correlation between VDR I polymorphism and the risk of pulmonary tuberculosis (PTB), and reported conflicting results. In the present study, an updated meta-analysis was performed to evaluate the above-said association. PubMed, Embase, and Google Scholar web-databases were searched for the relevant studies and a meta-analysis was performed by calculating pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) for all the genetic models. A total of 19 studies comprising 3644 controls and 2635 cases were included in the present study. Overall no association of PTB in allelic contrast (b compared with B: =0.285; OR =0.909, 95% CI =0.762-1.083), homozygous (bb compared with BB: =0.881; OR =0.975, 95% CI =0.700-1.359), heterozygous (bB compared with BB: =0.834; OR =1.017, 95% CI =0.872-1.185), dominant (bb compared with BB + Bb: =0.451; OR =0.954, 95% CI =0.843-1.079) and recessive (bb + Bb compared with BB: =0.983; OR =1.002, 95% CI =0.868-1.156) genetic models in comparison with wild-type allele and genotype BB were observed. However, variant allele (b compared with B: =0.001; OR =2.289, 95% CI =1.661-3.154) showed increased risk of PTB in Asians. In conclusion, VDR I polymorphism is not a risk factor for PTB in overall population. However, this polymorphism may be interrelated to an increased risk of PTB amongst Asians.
维生素D受体(VDR)基因3'端内含子8中的I(rs1544410)多态性已知参与mRNA稳定性的调节。许多研究评估了VDR I多态性与肺结核(PTB)风险之间的可能相关性,并报告了相互矛盾的结果。在本研究中,进行了一项更新的荟萃分析以评估上述关联。在PubMed、Embase和谷歌学术网络数据库中搜索相关研究,并通过计算所有遗传模型的合并比值比(OR)和95%置信区间(95%CI)进行荟萃分析。本研究共纳入19项研究,包括3644例对照和2635例病例。总体而言,在等位基因对比(b与B相比:=0.285;OR=0.909,95%CI=0.762-1.083)、纯合子(bb与BB相比:=0.881;OR=0.975,95%CI=0.700-1.359)、杂合子(bB与BB相比:=0.834;OR=1.017,95%CI=0.872-1.185)、显性(bb与BB+Bb相比:=0.451;OR=0.954,95%CI=0.843-1.079)和隐性(bb+Bb与BB相比:=0.983;OR=1.002,95%CI=0.868-1.156)遗传模型中,未观察到与野生型等位基因和基因型BB相比PTB的关联。然而,变异等位基因(b与B相比:=0.001;OR=2.289,95%CI=1.661-3.154)在亚洲人中显示出PTB风险增加。总之,VDR I多态性不是总体人群中PTB的危险因素。然而,这种多态性可能与亚洲人PTB风险增加有关。