脑外伤和高血压患者长期缺血性中风的风险

IF 1.8 Q3 CLINICAL NEUROLOGY
Farid Radmanesh, Saef Izzy, Ran S. Rotem, Zabreen Tahir, Quinn J. Rademaker, Taha Yahya, Ahmad Mashlah, Herman A. Taylor, Marc G. Weisskopf, Ross Zafonte, Aaron L. Baggish, R. Grashow
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引用次数: 0

摘要

创伤性脑损伤(TBI)与高血压和缺血性中风密切相关。本研究旨在确定创伤性脑损伤和高血压在创伤性脑损伤后中风发生中的相互作用。这项前瞻性研究使用了医院登记册来识别无并发症的患者。创伤性脑损伤患者(n = 3664)与非创伤性脑损伤患者(n = 1848)在年龄、性别和种族上进行了频率匹配。随访从创伤后或研究开始后 6 个月开始,长达 10 年。为了研究高血压在创伤后脑卒中中的作用,我们使用逻辑回归模型计算了四个暴露类别中脑卒中的效应估计值,其中包括创伤后脑卒中或高血压单独或合并暴露。其次,我们计算了将高血压视为中间因素的模型中创伤性脑损伤的条件直接效应(CDE)。第三,我们研究了创伤性脑损伤的影响是否会因服用降压药而改变。创伤性脑损伤组中风的 10 年累积发病率(4.7%)高于非创伤性脑损伤组(1.3%;P < 0.001)。发生高血压的创伤性脑损伤患者中风风险最高(几率比 [OR] = 4.83,95% 置信区间 [CI] = 2.53-9.23,p < 0.001)。综合效应估计值小于相加值,表明存在重叠的生物学途径。创伤性脑损伤的总效应(OR = 3.16,95% CI = 1.94-5.16,p < 0.001)高于考虑高血压的 CDE(OR = 2.45,95% CI = 0.93-6.47,p = 0.06)。抗高血压药物减弱了创伤性脑损伤的影响,表明创伤性脑损伤对中风的影响部分是通过高血压介导的。创伤性脑损伤是长期中风的一个独立危险因素,其潜在的生物学途径可能部分是通过创伤性脑损伤诱发的高血压来实现的。这些研究结果表明,筛查高血压可减轻创伤性脑损伤的中风风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Long-Term Ischemic Stroke in Patients With Traumatic Brain Injury and Incident Hypertension
Traumatic brain injury (TBI) is independently associated with hypertension and ischemic stroke. The goal of this study was to determine the interplay between TBI and incident hypertension in the occurrence of post-TBI stroke. This prospective study used a hospital-based registry to identify patients without pre-existing comorbidities. TBI patients (n = 3664) were frequency matched on age, sex, and race to non-TBI patients (n = 1848). Follow-up started 6 months post-TBI or study entry and extended up to 10 years. To examine hypertension's role in post-TBI stroke, we used logistic regression models to calculate the effect estimates for stroke in four exposure categories that included TBI or hypertension in isolation and in combination. Second, we calculated the conditional direct effect (CDE) of TBI in models that considered hypertension as intermediary. Third, we examined whether TBI effect was modified by antihypertensive medication use. The 10-year cumulative incidence of stroke was higher in the TBI group (4.7%) than the non-TBI group (1.3%; p < 0.001). TBI patients who developed hypertension had the highest risk of stroke (odds ratio [OR] = 4.83, 95% confidence interval [CI] = 2.53–9.23, p < 0.001). The combined effect estimates were less than additive, suggesting an overlapping biological pathway. The total effect of TBI (OR = 3.16, 95% CI = 1.94–5.16, p < 0.001) was higher than the CDE that accounted for hypertension (OR = 2.45, 95% CI = 0.93–6.47, p = 0.06). Antihypertensives attenuated the TBI effect, suggesting that the TBI effect on stroke is partially mediated through hypertension. TBI is an independent risk factor for long-term stroke, and the underlying biological pathway may partly operate through TBI-precipitated hypertension. These findings suggest that screening for hypertension may mitigate stroke risk in TBI.
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CiteScore
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