Department of Cerebrovascular Medicine (M.F.-D., M.K., S.Y., K.M., K.T.), National Cerebral and Cardiovascular Center, Suita, Japan.
Center for Advancing Clinical and Translational Sciences (M.F.-D., H.Y.), National Cerebral and Cardiovascular Center, Suita, Japan.
Stroke. 2020 Aug;51(8):2282-2286. doi: 10.1161/STROKEAHA.120.029770. Epub 2020 Jul 6.
Evidence regarding sex differences in clinical outcomes and treatment effect following intracerebral hemorrhage is limited. Using the ATACH-2 trial (Antihypertensive Treatment in Intracerebral Hemorrhage-2) data, we explored whether sex disparities exist in outcomes and response to intensive blood pressure (BP)-lowering therapy.
Eligible intracerebral hemorrhage subjects were randomly assigned to intensive (target systolic BP, 110-139 mm Hg) or standard (140-179 mm Hg) BP-lowering therapy within 4.5 hours after onset. Relative risk of death or disability corresponding to the modified Rankin Scale score of 4 to 6 was calculated, and interaction between sex and treatment was explored.
In total, 380 women and 620 men were included. Women were older, more prescribed antihypertensive drugs before onset, and had more lobar intracerebral hemorrhage than men. Hematoma expansion was observed less in women. After multivariable adjustment, the relative risk of death or disability in women was 1.19 (95% CI, 1.02-1.37, =0.023). The relative risk of death or disability between intensive versus standard BP-lowering therapy was 0.91 (95% CI, 0.74-1.13) in women versus 1.13 (95% CI, 0.92-1.39) in men ( for interaction=0.11), with inconclusive Gail-Simmon test (=0.16).
Women had a higher risk of death or disability following intracerebral hemorrhage. The benefit of intensive BP-lowering therapy in women is inconclusive, consistent with the overall results of ATACH-2. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01176565.
关于脑出血患者临床结局和治疗效果的性别差异证据有限。本研究使用 ATACH-2 试验(颅内出血-2 降压治疗试验)的数据,旨在探讨强化降压治疗是否存在性别差异。
符合条件的脑出血患者在发病后 4.5 小时内随机分为强化(目标收缩压 110-139mmHg)或标准(140-179mmHg)降压治疗组。计算改良 Rankin 量表评分 4-6 分的死亡或残疾相对风险,并探讨性别与治疗之间的交互作用。
共纳入 380 名女性和 620 名男性。女性年龄较大,发病前更常服用降压药,且更易发生脑叶出血。女性血肿扩大较少。多变量调整后,女性死亡或残疾的相对风险为 1.19(95%CI,1.02-1.37,=0.023)。女性强化降压治疗与标准降压治疗的死亡或残疾相对风险为 0.91(95%CI,0.74-1.13),男性为 1.13(95%CI,0.92-1.39)(交互作用=0.11),Gail-Simmon 检验不确定(=0.16)。
脑出血后女性死亡或残疾风险较高。强化降压治疗对女性的获益不确定,与 ATACH-2 的总体结果一致。注册:网址:https://www.clinicaltrials.gov。唯一标识符:NCT01176565。