Department of Neurology and Stroke Unit, Rothschild Foundation Hospital, Paris, France.
Clinical Research Unit, Rothschild Foundation Hospital, Paris, France.
Ann Clin Transl Neurol. 2024 Apr;11(4):916-925. doi: 10.1002/acn3.52008. Epub 2024 Jan 29.
The stroke risk for persons living with human immunodeficiency virus (PLHIVs) doubled compared to uninfected individuals. Stroke-unit (SU)-access, acute reperfusion therapy-use and outcome data on PLHIVs admitted for acute ischemic stroke (AIS) are scarce.
AIS patients admitted (01 January 2017 to 31 January 2021) to 10 representative Paris-area SUs were screened retrospectively from the National Hospitalization Database. PLHIVs were compared to age-, initial NIHSS- and sex-matched HIV-uninfected controls (HUCs). Outcome was the 90-day modified Rankin Scale score.
Among 126 PLHIVs with confirmed first-ever AIS, ~80% were admitted outside the thrombolysis-administration window. Despite antiretrovirals, uncontrolled plasma HIV loads exceeded 50 copies/mL (26% of all PLHIVs; 38% of those ≤55 years). PLHIVs' stroke causes by decreasing frequency were large artery atherosclerosis (LAA), undetermined, other cause, cerebral small-vessel disease (CSVD) or cardioembolism. No stroke etiology was associated with HIV duration or detectable HIVemia. MRI revealed previously unknown AIS in one in three PLHIVs, twice the HUC rate (p = 0.006). Neither group had optimally controlled modifiable cardiovascular risk factors (CVRFs): 20%-30% without specific hypertension, diabetes, and/or dyslipidemia treatments. Their stroke outcomes were comparable. Multivariable analyses retained good prognosis associated solely with initial NIHSS or reperfusion therapy. Older age and hypertension were associated with CSVD/LAA for all PLHIVs. Standard neurovascular care and reperfusion therapy were well-tolerated.
The high uncontrolled HIV-infection rate and suboptimal CVRF treatment support heightened vigilance to counter suboptimal HIV suppression and antiretroviral adherence, and improve CVRF prevention, mainly for younger PLHIVs. Those preventive, routine measures could lower PLHIVs' AIS risk.
与未感染人群相比,感染人类免疫缺陷病毒(HIV)的个体发生中风的风险增加了一倍。关于因急性缺血性中风(AIS)住院的 HIV 感染者(PLHIVs),中风单元(SU)的收治情况、急性再灌注治疗的使用情况以及预后数据都非常有限。
回顾性筛选了 2017 年 1 月 1 日至 2021 年 1 月 31 日期间,10 个具有代表性的巴黎地区中风单元收治的所有 AIS 患者,排除了重复住院和非首次 AIS 患者。将 PLHIVs 与年龄、初始 NIHSS 评分和性别相匹配的 HIV 未感染者(HUCs)进行比较。结局为 90 天改良 Rankin 量表评分。
在 126 例确诊为首次 AIS 的 PLHIVs 中,约 80% 的患者发病时已超过溶栓治疗时间窗。尽管接受了抗逆转录病毒治疗,但仍有 26%(所有 PLHIVs 中的 26%;≤55 岁的 PLHIVs 中的 38%)患者的血浆 HIV 载量未得到有效控制。PLHIVs 的中风病因依次为大动脉粥样硬化(LAA)、病因不明、其他原因、脑小血管疾病(CSVD)或心源性栓塞。HIV 持续时间或可检测到的 HIV 血症与任何一种中风病因均无关联。MRI 显示,三分之一的 PLHIVs 存在以前未被发现的 AIS,这一比例是 HUCs 的两倍(p=0.006)。两组均未对可改变的心血管危险因素(CVRFs)进行最佳控制:20%-30%的患者未接受特异性高血压、糖尿病和/或血脂异常治疗。两组患者的中风结局相当。多变量分析结果表明,仅有初始 NIHSS 评分或再灌注治疗与良好预后相关。高龄和高血压与所有 PLHIVs 的 CSVD/LAA 有关。所有患者均能良好耐受标准的神经血管治疗和再灌注治疗。
未得到有效控制的 HIV 感染率和 CVRF 治疗的不充分,提示我们需要提高对未得到有效抑制的 HIV 感染和不依从抗逆转录病毒治疗的警惕性,加强对 CVRF 的预防,特别是针对年轻的 PLHIVs。这些预防措施可以降低 PLHIVs 的 AIS 风险。