Bueno Angel, Becerril-Gaitan Andrea, Mokua Collins, Ramirez-Garcia Kristina, Nguyen Justin, Shaker Faris, Nguyen Tien, Dono Antonio, Blackburn Spiros, Chen Peng Roc, Dannenbaum Mark, Choi H Alex, Day Arthur L, Morcos Jacques J, Chen Ching-Jen
Vivian L. Smith Department of Neurosurgery, Mcgovern Medical School, The University of Texas Health Science Center at Houston, 6400 Fannin Street, Suite #2800, Houston, TX, 77030, USA.
Acta Neurochir (Wien). 2025 Apr 10;167(1):103. doi: 10.1007/s00701-025-06516-5.
Metformin is widely prescribed and has neuroprotective effects in animals, but its impact on brain injury after aneurysmal subarachnoid hemorrhage (aSAH) in humans is unclear.
This single-center retrospective review assessed patients with aSAH from 2009 to 2023, categorizing them based on pre-admission metformin use. The primary outcome was delayed cerebral ischemia (DCI), while secondary outcomes included in-hospital mortality, rebleeding, angiographic cerebral vasospasm (CVS), and favorable modified Rankin Scale (mRS) scores at discharge and the 3-month follow-up. Outcomes were analyzed using logistic regression. Sensitivity analysis was performed after excluding patients receiving comfort care.
A total of 900 patients were included (47 metformin and 853 non-metformin). DCI rates were similar between groups (38.3% vs. 29.3%, aOR = 1.06 [0.49-2.28]). Rebleeding rates were 4.3% for metformin users and 5.6% for non-users (aOR = 0.47 [0.09-2.51]). In-hospital mortality was 4.3% in metformin users vs. 9.7% in non-users (aOR = 0.47 [0.08-2.84]). Angiographic CVS was 38.3% in metformin users and 52.8% in non-users (aOR = 0.49 [0.23-1.05]), and at 7 days, CVS was 29.8% vs. 47.6% (aOR = 0.46 [0.21-1.01]). Sensitivity analysis showed similar DCI rates (39.1% vs. 30.9%, aOR = 0.98 [0.45-2.15]) but lower CVS at 7 days for metformin users (aOR = 0.44 [0.20-0.98]).
Metformin use before aSAH did not significantly affect the risk of DCI or CVS. However, after excluding comfort care patients, the findings are highly speculative of reduced CVS risk at 7 days post-aSAH. Rebleeding and mortality rates were similar across groups. Future research with larger, multi-institutional datasets is needed to better understand metformin's impact, particularly during and after aSAH.
二甲双胍被广泛应用于临床治疗,在动物实验中具有神经保护作用,但其对人类动脉瘤性蛛网膜下腔出血(aSAH)后脑损伤的影响尚不清楚。
本单中心回顾性研究评估了2009年至2023年期间的aSAH患者,根据入院前是否使用二甲双胍进行分类。主要结局为延迟性脑缺血(DCI),次要结局包括住院死亡率、再出血、血管造影性脑血管痉挛(CVS)以及出院时和3个月随访时改良Rankin量表(mRS)评分良好。采用逻辑回归分析结局。在排除接受舒适护理的患者后进行敏感性分析。
共纳入900例患者(47例使用二甲双胍,853例未使用)。两组间DCI发生率相似(38.3%对29.3%,调整后比值比[aOR]=1.06[0.49 - 2.28])。二甲双胍使用者再出血率为4.3%,未使用者为5.6%(aOR = 0.47[0.09 - 2.51])。二甲双胍使用者住院死亡率为4.3%,未使用者为9.7%(aOR = 0.47[0.08 - 2.84])。血管造影性CVS在二甲双胍使用者中为38.3%,未使用者中为52.8%(aOR = 0.49[0.23 - 1.05]),在第7天时,CVS分别为29.8%对47.6%(aOR = 0.46[0.21 - 1.01])。敏感性分析显示DCI发生率相似(39.1%对30.9%,aOR = 0.98[0.45 - 2.15]),但二甲双胍使用者在第7天时CVS较低(aOR = 0.44[0.20 - 0.98])。
aSAH前使用二甲双胍对DCI或CVS风险无显著影响。然而,在排除舒适护理患者后,研究结果高度推测aSAH后7天CVS风险降低。两组间再出血率和死亡率相似。需要未来更大规模的多机构数据集研究,以更好地了解二甲双胍的影响,特别是在aSAH期间和之后。