Sekar Praveen Kumar Chandra, Veerabathiran Ramakrishnan
Human Cytogenetics and Genomics Laboratory, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamil Nadu, India.
Ann Indian Acad Neurol. 2024 Nov 1;27(6):629-637. doi: 10.4103/aian.aian_443_24. Epub 2024 Nov 22.
Toll-like receptor ( TLR2 ) gene plays an important role in the pathogenesis of bacterial meningitis (such as meningococcal meningitis and pneumococcal meningitis). The association between TLR4 rs4986790 polymorphism and the susceptibility to bacterial meningitis has been extensively studied. However, the results of these studies remain inconsistent. Therefore, we performed a meta-analysis to evaluate the association between TLR4 rs4986790 polymorphism and the susceptibility to meningococcal meningitis and pneumococcal meningitis.
Google Scholar, Embase, and PubMed databases were searched for case-control studies on TLR4 polymorphisms and the risks of meningococcal meningitis and pneumococcal meningitis, published up to May 31, 2024. To assess the strength of the association between TLR4 polymorphism and meningococcal meningitis and pneumococcal meningitis, the odds ratios (ORs) with 95% confidence intervals (CIs) were used. The meta-analysis of the associations between the TLR4 rs4986790 polymorphism and meningococcal meningitis and pneumococcal meningitis was carried out under different genetic models. Meta-analyses were conducted using Cochrane RoB 2 tool and Metagenyo to calculate the ORs and 95% CIs. Fourteen published studies with 3599 cases and 7438 controls were included.
Overall, there was a strong correlation between TLR4 polymorphisms and meningococcal meningitis observed across three genetic models using a random-effects model: GG + GA vs. AA (OR: 0.34, 95% CI: 0.14-0.79, P = 0.01, I ² = 60%); GA vs. AA (OR: 0.34, 95% CI: 0.13-0.91, P = 0.03, I ² = 65%); and GG vs. AA (OR: 0.34, 95% CI: 0.14-0.78, P = 0.01, I ² = 59%). Conversely, a fixed-effects model also revealed a significant association in the G vs. A model (OR: 0.84, 95% CI: 0.73-0.96, P = 0.01, I ² = 38%). In pneumococcal meningitis, a fixed-effects model analysis demonstrated a significant association in the GG vs. AA model (OR: 0.35, 95% CI: 0.14-0.87, P = 0.02, I ² = 48%) respectively.
This meta-analysis showed a strong correlation between TLR4 rs4986790 polymorphism and susceptibility to meningococcal meningitis and pneumococcal meningitis. Further studies with diverse populations are needed to validate and strengthen these findings.
Toll样受体(TLR2)基因在细菌性脑膜炎(如脑膜炎球菌性脑膜炎和肺炎球菌性脑膜炎)的发病机制中起重要作用。TLR4 rs4986790多态性与细菌性脑膜炎易感性之间的关联已得到广泛研究。然而,这些研究结果仍不一致。因此,我们进行了一项荟萃分析,以评估TLR4 rs4986790多态性与脑膜炎球菌性脑膜炎和肺炎球菌性脑膜炎易感性之间的关联。
检索谷歌学术、Embase和PubMed数据库,查找截至2024年5月31日发表的关于TLR4多态性与脑膜炎球菌性脑膜炎和肺炎球菌性脑膜炎风险的病例对照研究。为评估TLR4多态性与脑膜炎球菌性脑膜炎和肺炎球菌性脑膜炎之间关联的强度,使用了具有95%置信区间(CI)的比值比(OR)。在不同遗传模型下对TLR4 rs4986790多态性与脑膜炎球菌性脑膜炎和肺炎球菌性脑膜炎之间的关联进行荟萃分析。使用Cochrane RoB 2工具和Metagenyo进行荟萃分析,以计算OR和95% CI。纳入了14项已发表的研究,共3599例病例和7438例对照。
总体而言,使用随机效应模型在三种遗传模型中观察到TLR4多态性与脑膜炎球菌性脑膜炎之间存在强相关性:GG + GA与AA相比(OR:0.34,95% CI:0.14 - 0.79,P = 0.01,I² = 60%);GA与AA相比(OR:0.34,95% CI:0.13 - 0.91,P = 0.03,I² = 65%);以及GG与AA相比(OR:0.34,95% CI:0.14 - 0.78,P = 0.01,I² = 59%)。相反,固定效应模型在G与A模型中也显示出显著关联(OR:0.84,95% CI:0.73 - 0.96,P = 0.01,I² = 38%)。在肺炎球菌性脑膜炎中,固定效应模型分析分别在GG与AA模型中显示出显著关联(OR:0.35,95% CI:0.14 - 0.87,P = 0.02,I² = 48%)。
这项荟萃分析表明TLR4 rs4986790多态性与脑膜炎球菌性脑膜炎和肺炎球菌性脑膜炎易感性之间存在强相关性。需要对不同人群进行进一步研究以验证和加强这些发现。