Department of Neurosurgery, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie, 514-8507, Japan.
Center for Vessels and Heart, Mie University Hospital, Tsu, Japan.
Transl Stroke Res. 2019 Aug;10(4):381-388. doi: 10.1007/s12975-018-0650-y. Epub 2018 Jul 23.
Cilostazol is a selective inhibitor of phosphodiesterase type III that downregulates tenascin-C (TNC), a matricellular protein, which may cause delayed cerebral infarction after aneurysmal subarachnoid hemorrhage (SAH). The authors increased the dosage and evaluated the dose-dependent effects of cilostazol on delayed cerebral infarction and outcomes in SAH patients. This was a retrospective cohort study in a single center. One hundred fifty-six consecutive SAH patients including 67 patients of admission World Federation of Neurological Surgeons grades IV-V who underwent aneurysmal obliteration within 48 h post-SAH from 2007 to 2017 were analyzed. Cilostazol (0 to 300 mg/day) was administered from 1-day post-clipping or post-coiling to day 14 or later. Cilostazol treatment dose-dependently decreased delayed cerebral infarction and tended to improve outcomes, although cilostazol did not affect other outcome measures including angiographic vasospasm. On multivariate analyses, 300 mg/day (100 mg three times) cilostazol independently decreased delayed cerebral infarction and improved 3-month outcomes, but other regimens including 200 mg/day (100 mg twice) cilostazol were not independent prognostic factors. Propensity score-matched analyses showed that the 300 mg/day cilostazol cohort had lower plasma TNC levels and a lower incidence of delayed cerebral infarction associated with better outcomes compared with the non-cilostazol cohort. The 300 mg/day cilostazol may improve post-SAH outcomes by reducing plasma TNC levels and delayed cerebral infarction, but not vasospasm. Further studies are warranted to investigate if 300 mg/day cilostazol is more beneficial to post-SAH outcomes than a usual dose of 200 mg/day cilostazol that was demonstrated to be effective in randomized controlled trials.
西洛他唑是一种磷酸二酯酶 III 型选择性抑制剂,可下调细胞外基质蛋白 tenascin-C(TNC),后者可能导致蛛网膜下腔出血(SAH)后迟发性脑梗死。作者增加了剂量,并评估了西洛他唑对 SAH 患者迟发性脑梗死和结局的剂量依赖性影响。这是一项在单中心进行的回顾性队列研究。分析了 2007 年至 2017 年期间 156 例连续接受动脉瘤夹闭或栓塞治疗的 SAH 患者,这些患者在发病后 48 小时内入院,世界神经外科学会分级为 IV-V 级。西洛他唑(0 至 300mg/天)从夹闭或栓塞后 1 天开始给药,持续 14 天或更长时间。西洛他唑治疗剂量与迟发性脑梗死呈剂量依赖性降低,并趋于改善结局,尽管西洛他唑对血管痉挛等其他结局指标无影响。多变量分析显示,300mg/天(100mg,每日 3 次)西洛他唑可独立降低迟发性脑梗死和改善 3 个月结局,但 200mg/天(100mg,每日 2 次)等其他方案不是独立的预后因素。倾向评分匹配分析显示,与非西洛他唑组相比,300mg/天西洛他唑组的血浆 TNC 水平较低,迟发性脑梗死发生率较低,结局较好。300mg/天西洛他唑可能通过降低血浆 TNC 水平和迟发性脑梗死来改善 SAH 后的结局,但不改善血管痉挛。还需要进一步的研究来确定 300mg/天的西洛他唑是否比已在随机对照试验中证明有效的 200mg/天的西洛他唑更有益于 SAH 后的结局。