Neurosurgery Unit, Department of Clinical-Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy.
Department of Neurological Surgery, Hospital San Fernando, Buenos Aires, Argentina, .
Acta Biomed. 2022 Mar 21;92(S4):e2021420. doi: 10.23750/abm.v92iS4.12669.
Introduction The interleukin-6 (IL-6), a proinflammatory cytokine, supports the adaptive immune response and regulates inflammatory processes. The -174 G>C and -572 G>C promoter polymorphisms of the IL-6 gene take part in the pathogenesis of intracranial aneurysms (IAs) and influence the clinical presentation of subarachnoid hemorrhage. This meta-analysis purposes to evaluate whether and which IL-6 allelic variations are related to a risk of IAs formation. Methods A PRISMA-based literature search was performed on the PubMed/Medline and Web of Science databases. The keywords used were "interleukin-6," "IL-6," "polymorphism," "interleukin-6 genotype," combined with "intracranial aneurysms" and "subarachnoid hemorrhage." Only human case-control studies, with a study (IAs) and a control group, written in English, and published in the last 15 years were selected. A meta-analysis was performed, estimating odds ratios and 95% confidence intervals in fixed- or random-effects models, as applicable. Statistical analysis was conducted with RevMan 5.0 software. Results 9 studies were eligible. No associations were found between -174 G>C polymorphisms and IAs susceptibility. Notable results were reported by the analysis of -572G>C polymorphisms. -572GG/GC/CC genotypes were strongly related to IAs occurrence with a statistical significance of p=0.03, p=0.0009, and p=0.00001, respectively. Conclusion A higher incidence of -572G>C promoter polymorphisms were demonstrated in the IAs group, highlighting the pivotal role of inflammatory genes in the natural history of brain aneurysms. Additional studies are required considering the racial heterogenicity and the need to widen the population sample.
白细胞介素-6(IL-6)是一种促炎细胞因子,它支持适应性免疫反应并调节炎症过程。IL-6 基因的-174 G>C 和-572 G>C 启动子多态性参与颅内动脉瘤(IA)的发病机制,并影响蛛网膜下腔出血的临床表现。本荟萃分析旨在评估 IL-6 等位基因变异是否与 IA 形成的风险相关。
根据 PRISMA 原则,在 PubMed/Medline 和 Web of Science 数据库中进行文献检索。使用的关键词是“白细胞介素-6”、“IL-6”、“多态性”、“白细胞介素-6 基因型”,与“颅内动脉瘤”和“蛛网膜下腔出血”相结合。仅选择以英语撰写、发表于过去 15 年、为人类病例对照研究且包含病例组和对照组的研究。采用固定或随机效应模型进行荟萃分析,估计比值比和 95%置信区间。使用 RevMan 5.0 软件进行统计分析。
有 9 项研究符合纳入标准。-174 G>C 多态性与 IA 易感性之间没有关联。-572G>C 多态性分析报告了显著结果。-572GG/GC/CC 基因型与 IA 的发生具有显著相关性,p 值分别为 0.03、0.0009 和 0.00001。
IA 组中-572G>C 启动子多态性的发生率较高,这突显了炎症基因在脑动脉瘤自然史中的关键作用。需要考虑种族异质性和扩大人群样本,进行更多的研究。