From the Department of Radiology (A.P.), 401 General Military Hospital of Athens; National Public Health Organization (K.P.), Athens, Greece; Department of Clinical Sciences Malmö (H.B.), Lund University, Sweden; Institute of Epidemiology (A.P.), Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg; German Center for Diabetes Research (DZD) (A.P.), München-Neuherberg, Neuherberg; German Research Center for Cardiovascular Disease (DZHK) (A.P.), Partner Site Munich Heart Alliance; Institute of Medical Information Sciences, Biometry and Epidemiology (A.P.), and Institute for Stroke and Dementia Research, University Hospital (M.D., M.K.G.), Ludwig-Maximilians-University, Munich, Germany; Division of Cardiology (J.A.d.L.), University of Texas Southwestern Medical Center, Dallas; National Heart, Lung, and Blood Institute's and Boston University's Framingham Heart Study (S.S.), Framingham; Department of Medicine (S.S.), Boston University School of Medicine, MA; Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases (S.S.), University of Texas Health Sciences Center, San Antonio; Munich Cluster for Systems Neurology (SyNergy) (M.D.); and German Centre for Neurodegenerative Diseases (DZNE) (M.D.), Munich, Germany. M.K.G. is currently at the Center for Genomic Medicine, Massachusetts General Hospital, Boston and the Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA.
Neurology. 2022 Mar 8;98(10):e1002-e1012. doi: 10.1212/WNL.0000000000013274. Epub 2021 Dec 30.
Human genetic studies support a key role of interleukin-6 (IL-6) in the pathogenesis of ischemic stroke. However, there are only limited data from observational studies exploring circulating IL-6 levels as a risk factor for ischemic stroke. We set out to perform a systematic review and meta-analysis of aggregate data on cohort studies to determine the magnitude and shape of the association between circulating IL-6 levels and risk of incident ischemic stroke in the general population.
Following the PRISMA guidelines, we systematically screened the PubMed search engine from inception to March 2021 for population-based prospective cohort studies exploring the association between circulating IL-6 levels and risk of incident ischemic stroke. We pooled association estimates for ischemic stroke risk with random-effects models and explored nonlinear effects in dose-response meta-analyses. Risk of bias was assessed with the Newcastle-Ottawa Scale (NOS). We used funnel plots and trim-to-fill analyses to assess publication bias.
We identified 11 studies (n = 27,411 individuals; 2,669 stroke events) meeting our eligibility criteria. Mean age of all included participants was 60.5 years and 54.8% were female. Overall, quality of the included studies was high (median 8 out of 9 NOS points, interquartile range 7-9). In meta-analyses, 1 SD increment in circulating log-transformed IL-6 levels was associated with a 19% increase in risk of incident ischemic stroke over a mean follow-up of 12.4 years (relative risk 1.19; 95% confidence interval 1.10 to 1.28). A dose-response meta-analysis showed a linear association between circulating IL-6 levels and ischemic stroke risk. There was only moderate heterogeneity and the results were consistent in sensitivity analyses restricted to studies of low risk of bias and studies fully adjusting for demographic and vascular risk factors. The results also remained stable following adjustment for publication bias.
Higher circulating IL-6 levels in community-dwelling individuals are associated with higher long-term risk of incident ischemic stroke in a linear pattern and independently of conventional vascular risk factors. Along with findings from genetic studies and clinical trials, these results provide additional support for a key role of IL-6 signaling in ischemic stroke.
人类遗传学研究支持白细胞介素 6(IL-6)在缺血性脑卒中发病机制中的关键作用。然而,仅有少数观察性研究的有限数据探讨了循环 IL-6 水平作为缺血性脑卒中风险因素的作用。我们旨在进行系统综述和荟萃分析,以确定人群队列研究中汇总数据中循环 IL-6 水平与普通人群中缺血性脑卒中风险之间的关联程度和形状。
根据 PRISMA 指南,我们从成立到 2021 年 3 月,系统地在 PubMed 搜索引擎中筛选了探索循环 IL-6 水平与缺血性脑卒中风险之间关联的基于人群的前瞻性队列研究。我们采用随机效应模型汇总缺血性脑卒中风险的关联估计,并在剂量-反应荟萃分析中探索非线性效应。使用纽卡斯尔-渥太华量表(NOS)评估偏倚风险。我们使用漏斗图和修剪填充分析来评估发表偏倚。
我们确定了 11 项符合纳入标准的研究(n=27411 人;2669 例脑卒中事件)。所有纳入参与者的平均年龄为 60.5 岁,54.8%为女性。总体而言,纳入研究的质量较高(中位数为 9 分 NOS 评分中的 8 分,四分位距为 7-9 分)。荟萃分析显示,循环 log 转换 IL-6 水平每增加 1 个标准差,在平均 12.4 年的随访中,缺血性脑卒中风险增加 19%(相对风险 1.19;95%置信区间 1.10 至 1.28)。剂量-反应荟萃分析显示,循环 IL-6 水平与缺血性脑卒中风险之间存在线性关联。异质性适中,在仅纳入低偏倚风险研究和充分调整人口统计学和血管风险因素的研究的敏感性分析中结果一致。在调整发表偏倚后,结果仍然稳定。
在社区居住的个体中,循环 IL-6 水平较高与线性模式下的长期缺血性脑卒中事件风险增加相关,并且独立于传统的血管风险因素。这些结果与遗传研究和临床试验的结果一起,为 IL-6 信号在缺血性脑卒中中的关键作用提供了额外的支持。