Kubiszewski Patryk, Sugita Lansing, Kourkoulis Christina, DiPucchio Zora, Schwab Kristin, Anderson Christopher D, Gurol M Edip, Greenberg Steven M, Viswanathan Anand, Rosand Jonathan, Biffi Alessandro
Hemorrhagic Stroke Research Program, J. Philip Kistler Stroke Research Center, Boston, Massachusetts.
Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts.
JAMA Neurol. 2020 Aug 31;78(1):1-8. doi: 10.1001/jamaneurol.2020.3142.
Selective serotonin reuptake inhibitors (SSRIs) are widely used to treat poststroke depression but are associated with increased incidence of first-ever intracerebral hemorrhage (ICH) in the general population. The decision to treat ICH survivors with SSRIs must therefore balance potential risks of ICH recurrence with presumed benefits on depressive symptoms.
To determine whether SSRI use among survivors of primary ICH was associated with ICH recurrence and decreased severity of depressive symptoms.
DESIGN, SETTING, AND PARTICIPANTS: Longitudinal ICH cohort study at a tertiary care center enrolling from January 2006 to December 2017, with follow-up for a median of 53.2 months (interquartile range, 42.3-61.2 months). The study included 1279 consenting individuals (1049 White, 89 Black, 77 Hispanic, and 64 other race/ethnicity) of 1335 eligible patients presenting with primary ICH and who were discharged alive from initial hospitalization for stroke.
We conducted univariable and multivariable analyses for ICH recurrence risk and depression severity, including subset analyses for patients with 1 or more of the following characteristics associated with high ICH recurrence risk: (1) lobar ICH; (2) presence of the apolipoprotein ε2/ε4 gene variants; (3) prior history of ICH/TIA/ischemic stroke; and (4) Black or Hispanic race/ethnicity.
Mean age of study participants was 71.3 years, with 602 women (47%); of the 1279 participants, 1049 were White, 89 were Black, 77 were Hispanic, and 64 were other race/ethnicity. SSRI exposure was associated with both ICH recurrence (subhazard ratio [SHR], 1.31; 95% CI, 1.08-1.59) and resolution of post-ICH depression (SHR, 1.53; 95% CI, 1.12 2.09). Among those individuals at high risk for recurrent ICH, SSRIs were associated with further elevation in risk for ICH recurrence (SHR, 1.79; 95% CI, 1.22-2.64) compared with all other survivors of ICH (SHR, 1.20; 95% CI, 1.01-1.42; P = .008 for comparison of effect sizes). The association of SSRI with reduced depressive symptoms did not differ between high those at high risk for recurrent ICH and all other ICH survivors.
Selective serotonin reuptake inhibitor exposure after ICH is associated with both improvement in depressive symptoms and increased risk of recurrent hemorrhagic stroke. Clinical history, neuroimaging data, and genetic biomarkers may help to identify survivors of ICH more likely to safely tolerate SSRI use.
选择性5-羟色胺再摄取抑制剂(SSRI)被广泛用于治疗中风后抑郁症,但在普通人群中与首次脑出血(ICH)的发病率增加相关。因此,决定用SSRI治疗ICH幸存者时,必须在ICH复发的潜在风险与对抑郁症状的假定益处之间取得平衡。
确定原发性ICH幸存者使用SSRI是否与ICH复发及抑郁症状严重程度降低相关。
设计、地点和参与者:在一家三级医疗中心进行的纵向ICH队列研究,从2006年1月至2017年12月招募患者,中位随访时间为53.2个月(四分位间距,42.3 - 61.2个月)。该研究纳入了1335例符合条件的原发性ICH患者中1279例同意参与的个体(1049例白人、89例黑人、77例西班牙裔和64例其他种族/族裔),这些患者因中风首次住院后存活出院。
我们对ICH复发风险和抑郁严重程度进行了单变量和多变量分析,包括对具有以下1种或多种与高ICH复发风险相关特征的患者进行亚组分析:(1)脑叶ICH;(2)载脂蛋白ε2/ε4基因变异的存在;(3)既往ICH/TIA/缺血性中风病史;(4)黑人或西班牙裔种族/族裔。
研究参与者的平均年龄为71.3岁,其中602例为女性(47%);在1279例参与者中,1049例为白人,89例为黑人,77例为西班牙裔,64例为其他种族/族裔。SSRI暴露与ICH复发(亚风险比[SHR],1.31;95%置信区间,1.08 - 1.59)及ICH后抑郁症缓解(SHR,1.53;95%置信区间,1.12 - 2.09)均相关。在那些ICH复发高风险个体中,与所有其他ICH幸存者相比,SSRI与ICH复发风险进一步升高相关(SHR,1.79;95%置信区间,1.22 - 2.64)(效应大小比较的P = 0.008)。SSRI与抑郁症状减轻的关联在ICH复发高风险者和所有其他ICH幸存者之间无差异。
ICH后使用选择性5-羟色胺再摄取抑制剂与抑郁症状改善及复发性出血性中风风险增加均相关。临床病史、神经影像学数据和基因生物标志物可能有助于识别更有可能安全耐受使用SSRI的ICH幸存者。