Areeshi Mohammed Y, Mandal Raju K, Akhter Naseem, Dar Sajad A, Jawed Arshad, Wahid Mohd, Mahto Harishankar, Panda Aditya K, Lohani Mohtashim, Haque Shafiul
Research and Scientific Studies Unit, College of Nursing &Allied Health Sciences, Jazan University, Jazan-45142, Saudi Arabia.
Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Albaha University, Albaha-65431, Saudi Arabia.
Sci Rep. 2016 Nov 23;6:35728. doi: 10.1038/srep35728.
MBL2 gene encodes mannose-binding lectin, is a member of innate immune system. Earlier studies revealed that MBL2 gene variants, rs1800451, rs1800450, rs5030737, rs7096206, rs11003125 and rs7095891 are associated with impaired serum level and susceptibility to TB, but their results are inconsistent. A meta-analysis was performed by including 22 studies (7095 TB-patients and 7662 controls) and data were analyzed with respect to associations between alleles, genotypes and minor allele carriers to evaluate the potential association between MBL2 polymorphisms and TB risk. Statistically significant results were found only for the homozygous variant genotype (CC vs. AA: p = 0.045; OR = 0.834, 95% CI = 0.699 to 0.996) of rs1800451 and showed reduced risk of TB in overall population. However, other genetic models of rs1800450, rs5030737, rs7096206, rs11003125, rs7095891 and combined rs1800450, rs1800451, rs5030737 polymorphisms of MBL2 gene did not reveal any association with TB risk. Stratified analysis by ethnicity showed decreased risk of TB in African population for rs1800450 and rs1800451. Whereas, no association was observed between other MBL2 polymorphisms and TB risk in all the evaluated ethnic populations. In conclusion, MBL2 rs1800450 and rs1800451 polymorphisms play a protective role in TB infection and reinforce their critical significance as a potential genetic marker for TB resistance.
MBL2基因编码甘露糖结合凝集素,是先天免疫系统的一员。早期研究表明,MBL2基因变异体rs1800451、rs1800450、rs5030737、rs7096206、rs11003125和rs7095891与血清水平受损和结核病易感性相关,但结果并不一致。纳入22项研究(7095例结核病患者和7662例对照)进行荟萃分析,并就等位基因、基因型和次要等位基因携带者之间的关联分析数据,以评估MBL2基因多态性与结核病风险之间的潜在关联。仅发现rs1800451的纯合变异基因型(CC与AA:p = 0.045;OR = 0.834,95% CI = 0.699至0.996)具有统计学显著结果,且显示总体人群中结核病风险降低。然而,rs1800450、rs5030737、rs7096206、rs11003125、rs7095891的其他遗传模型以及MBL2基因的rs1800450、rs1800451、rs5030737多态性组合均未显示与结核病风险存在任何关联。按种族进行的分层分析显示,rs1800450和rs1800451在非洲人群中结核病风险降低。而在所有评估的种族人群中,未观察到其他MBL2多态性与结核病风险之间存在关联。总之,MBL2 rs1800450和rs1800451多态性在结核病感染中起保护作用,并强化了它们作为结核病抗性潜在遗传标志物的关键意义。