Dipartimento di Scienze Cliniche e Sperimentali, Clinica Neurologica, Università degli Studi di Brescia, Italy (S.B., M.L., V.M., D.P., A. Padovani, A. Pezzini).
Dipartimento di Scienze del Sistema Nervoso e del Comportamento, Unità di Statistica Medica e Genomica, Università di Pavia, Italy (M. Grassi).
Stroke. 2021 Mar;52(3):821-829. doi: 10.1161/STROKEAHA.120.031579. Epub 2021 Jan 28.
Observational studies have suggested a link between fibromuscular dysplasia and spontaneous cervical artery dissection (sCeAD). However, whether patients with coexistence of the two conditions have distinctive clinical characteristics has not been extensively investigated.
In a cohort of consecutive patients with first-ever sCeAD, enrolled in the setting of the multicenter IPSYS CeAD study (Italian Project on Stroke in Young Adults Cervical Artery Dissection) between January 2000 and June 2019, we compared demographic and clinical characteristics, risk factor profile, vascular pathology, and midterm outcome of patients with coexistent cerebrovascular fibromuscular dysplasia (cFMD; cFMD+) with those of patients without cFMD (cFMD-).
A total of 1283 sCeAD patients (mean age, 47.8±11.4 years; women, 545 [42.5%]) qualified for the analysis, of whom 103 (8.0%) were diagnosed with cFMD+. In multivariable analysis, history of migraine (odds ratio, 1.78 [95% CI, 1.13-2.79]), the presence of intracranial aneurysms (odds ratio, 8.71 [95% CI, 4.06-18.68]), and the occurrence of minor traumas before the event (odds ratio, 0.48 [95% CI, 0.26-0.89]) were associated with cFMD. After a median follow-up of 34.0 months (25th to 75th percentile, 60.0), 39 (3.3%) patients had recurrent sCeAD events. cFMD+ and history of migraine predicted independently the risk of recurrent sCeAD (hazard ratio, 3.40 [95% CI, 1.58-7.31] and 2.07 [95% CI, 1.06-4.03], respectively) in multivariable Cox proportional hazards analysis.
Risk factor profile of sCeAD patients with cFMD differs from that of patients without cFMD. cFMD and migraine are independent predictors of midterm risk of sCeAD recurrence.
观察性研究表明,纤维肌发育不良与自发性颈内动脉夹层(sCeAD)之间存在关联。然而,同时存在这两种情况的患者是否具有独特的临床特征尚未得到广泛研究。
在 2000 年 1 月至 2019 年 6 月期间,多中心 IPSYS CeAD 研究(意大利青年卒中颈内动脉夹层研究)连续纳入的首次 sCeAD 患者队列中,我们比较了同时存在脑血管纤维肌发育不良(cFMD;cFMD+)的患者与不存在 cFMD 的患者(cFMD-)的人口统计学和临床特征、危险因素谱、血管病理学和中期结局。
共有 1283 例 sCeAD 患者(平均年龄 47.8±11.4 岁;女性 545 例[42.5%])符合分析条件,其中 103 例(8.0%)诊断为 cFMD+。多变量分析显示,偏头痛史(比值比,1.78[95%可信区间,1.13-2.79])、颅内动脉瘤(比值比,8.71[95%可信区间,4.06-18.68])和事件前发生轻微创伤(比值比,0.48[95%可信区间,0.26-0.89])与 cFMD 相关。中位随访 34.0 个月(25 至 75 分位数,60.0)后,39 例(3.3%)患者发生 sCeAD 复发事件。多变量 Cox 比例风险分析显示,cFMD+和偏头痛史独立预测 sCeAD 复发的风险(风险比,3.40[95%可信区间,1.58-7.31]和 2.07[95%可信区间,1.06-4.03])。
cFMD 合并 sCeAD 患者的危险因素谱与无 cFMD 的患者不同。cFMD 和偏头痛是 sCeAD 复发中期风险的独立预测因素。