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FADD(死亡结构域相关 Fas 蛋白)、Caspase-3 和 Caspase-8 与缺血性脑卒中的发生。

FADD (Fas-Associated Protein With Death Domain), Caspase-3, and Caspase-8 and Incidence of Ischemic Stroke.

机构信息

From the Department of Clinical Sciences, Lund University, Malmö, Sweden (I.F.M., Y.B., O.M., M.O.-M., J.N., M.S., G.E.).

Skåne University Hospital, Malmö, Sweden (O.M., J.N., M.S.).

出版信息

Stroke. 2018 Sep;49(9):2224-2226. doi: 10.1161/STROKEAHA.118.022063.

Abstract

Background and Purpose- Apoptosis has been implicated in atherosclerosis and plaque rupture. This population-based study examined the relationship between 3 markers of apoptosis, that is, FADD (Fas-associated protein with death domain), caspase-3, and caspase-8, and incidence of ischemic stroke. Methods- The study population included 4356 participants from the MDCS (Malmö Diet and Cancer Study) cardiovascular cohort, without a history of stroke. Incidence of ischemic stroke was followed by linkages to local and national registers. Cox proportional hazards regression was used to assess the incidence of ischemic stroke in relation to quartiles of FADD, caspase-3, and caspase-8, adjusted for potential confounders. Results- During a mean follow-up period of 19.5±4.9 years, a total of 321 (7.4%) participants were diagnosed with incident ischemic stroke. Individuals with high levels of FADD and caspase-8 had a significantly increased risk of ischemic stroke, after adjustment for potential confounders. The multivariable-adjusted hazard ratios for Q4 versus Q1-Q3 of FADD and caspase-8 were 1.49 (95% CI, 1.18-1.87; P<0.01) and 1.77 (95% CI, 1.41-2.22; P<0.001), respectively. The hazard ratios per 1-SD increment of FADD and caspase-8 were 1.27 (95% CI, 1.14-1.41) and 1.31 (95% CI, 1.18-1.45), respectively. No association was observed for caspase-3 with ischemic stroke. Conclusions- Elevated levels of FADD and caspase-8, but not caspase-3, are associated with increased incidence of ischemic stroke.

摘要

背景与目的-细胞凋亡与动脉粥样硬化和斑块破裂有关。本项基于人群的研究旨在探讨 Fas 相关死亡结构域蛋白(FADD)、半胱氨酸天冬氨酸蛋白酶-3(caspase-3)和 caspase-8 这 3 种凋亡标志物与缺血性卒中发病之间的关系。方法-该研究人群来自马尔默饮食与癌症研究(MDCS)心血管队列,共 4356 例,均无卒中病史。通过与当地和国家登记处的链接来随访缺血性卒中的发病情况。采用 Cox 比例风险回归评估 FADD、caspase-3 和 caspase-8 四分位间距与缺血性卒中发病之间的关系,并校正潜在混杂因素。结果-平均随访 19.5±4.9 年后,共有 321 例(7.4%)参与者被诊断为新发缺血性卒中。校正潜在混杂因素后,高水平的 FADD 和 caspase-8 与缺血性卒中风险显著增加相关。FADD 和 caspase-8 第 4 四分位间距与第 1-3 四分位间距的多变量校正后风险比分别为 1.49(95%CI,1.18-1.87;P<0.01)和 1.77(95%CI,1.41-2.22;P<0.001)。FADD 和 caspase-8 每增加 1-SD,风险比分别为 1.27(95%CI,1.14-1.41)和 1.31(95%CI,1.18-1.45)。caspase-3 与缺血性卒中之间无关联。结论-FADD 和 caspase-8 水平升高(而非 caspase-3)与缺血性卒中发病率增加有关。

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