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双重抗血小板治疗与阿替普酶治疗轻度非致残性急性缺血性卒中患者的性别差异:ARAMIS研究的二次分析

Sex Differences in the Dual Antiplatelet Therapy Versus Alteplase for Patients with Minor Nondisabling Acute Ischemic Stroke: A Secondary Analysis of the ARAMIS Study.

作者信息

Qu Hui-Ling, Sun Xiao-Yu, He Chao, Chen Hui-Sheng

机构信息

Department of Neurology, The General Hospital of Northern Theater Command, Shenyang, 110016, China.

出版信息

CNS Drugs. 2024 Aug;38(8):649-659. doi: 10.1007/s40263-024-01096-x. Epub 2024 May 28.

Abstract

BACKGROUND AND PURPOSE

Sex is associated with clinical outcome in stroke. The present study aimed to determine the effect of sex on efficacy of dual antiplatelet (DAPT) versus alteplase in ischemic stroke based on Antiplatelet versus recombinant tissue plasminogen activator (R-tPA) for Acute Mild Ischemic Stroke (ARAMIS) trial.

METHODS

In this secondary analysis of the ARAMIS study, eligible patients aged 18 years or older with minor nondisabling stroke who received dual antiplatelet therapy or intravenous alteplase within 4.5 h of stroke onset were divided into two groups: men and women. The primary endpoint was an excellent functional outcome, defined as a modified Rankin Scale (mRS) 0-1 at 90 days. Binary logistic regression analyses and generalized linear models were used.

RESULTS

Of the 719 patients who completed the study, 31% (223) were women, and 69% (496) were men. There were no significant sex differences in excellent functional outcome (unadjusted p = 0.304 for men and p = 0.993 for women; adjusted p = 0.376 for men and p = 0.918 for women) and favorable functional outcome (mRS score of 0-2; unadjusted p = 0.968 for men and p = 0.881 for women; adjusted p = 0.824 for men and p = 0.881 for women). But for the secondary outcomes, compared with alteplase, DAPT was associated with a significantly decreased proportion of early neurological deterioration within 24 h in men {unadjusted odds ratio [OR] = 0.440 [95% confidence interval (CI), 0.221-0.878]; p = 0.020; adjusted OR = 0.436 [95% CI, 0.216-0.877]; p = 0.020}, but not in women [unadjusted OR = 0.636 (95% CI, 0.175-2.319), p = 0.490; adjusted OR = 0.687 (95% CI, 0.181-2.609), p = 0.581]. For the safety outcomes, compared with the DAPT group, alteplase was associated with a significantly increased proportion of any bleeding events in men [unadjusted OR = 3.110 (95% CI, 1.103-8.770); p = 0.032], but not in women [unadjusted OR = 5.333 (95% CI, 0.613-46.407), p = 0.129; adjusted OR = 5.394 (95% CI, 0.592-49.112), p = 0.135].

CONCLUSION

Sex did not influence the effect of dual antiplatelet therapy versus intravenous alteplase in minor nondisabling stroke, but more early neurological deterioration and bleeding events occurred in men who received alteplase.

摘要

背景与目的

性别与卒中的临床结局相关。本研究旨在基于急性轻度缺血性卒中抗血小板治疗与重组组织型纤溶酶原激活剂(R-tPA)对比试验(ARAMIS),确定性别对缺血性卒中双重抗血小板治疗(DAPT)与阿替普酶疗效的影响。

方法

在ARAMIS研究的这项二次分析中,年龄在18岁及以上、患有轻度非致残性卒中且在卒中发作后4.5小时内接受双重抗血小板治疗或静脉注射阿替普酶的符合条件患者被分为两组:男性和女性。主要终点是良好的功能结局,定义为90天时改良Rankin量表(mRS)评分为0 - 1分。采用二元逻辑回归分析和广义线性模型。

结果

在完成研究的719例患者中,31%(223例)为女性,69%(496例)为男性。在良好的功能结局方面(未调整时男性p = 0.304,女性p = 0.993;调整后男性p = 0.376,女性p = 0.918)以及有利的功能结局(mRS评分为0 - 2分;未调整时男性p = 0.968,女性p = 0.881;调整后男性p = 0.824,女性p = 0.881)方面,性别差异均无统计学意义。但对于次要结局,与阿替普酶相比,DAPT使男性在24小时内早期神经功能恶化的比例显著降低(未调整比值比[OR] = 0.440 [95%置信区间(CI),0.221 - 0.878];p = 0.020;调整后OR = 0.436 [95% CI,0.216 - 0.877];p = 0.020),而女性则无此差异[未调整OR = 0.636(95% CI,0.175 - 2.319),p = 0.490;调整后OR = 0.687(95% CI,0.181 - 2.609),p = 0.581]。在安全性结局方面,与DAPT组相比,阿替普酶使男性发生任何出血事件的比例显著增加[未调整OR = 3.110(95% CI,1.103 - 8.770);p = 0.032],而女性则无此差异[未调整OR = 5.333(95% CI,0.613 - 46.407),p = 0.129;调整后OR = 5.394(95% CI,0.592 - 49.112),p = 0.135]。

结论

性别不影响轻度非致残性卒中双重抗血小板治疗与静脉注射阿替普酶的疗效,但接受阿替普酶治疗的男性发生更多早期神经功能恶化和出血事件。

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