The Etiology of Intracranial Artery Stenosis in Autoimmune Rheumatic Diseases: An Observational High-Resolution MR Imaging Study.

Shun Li, Qiuyu Yu, Yangzhong Zhou, Manqiu Ding, Huanyu Zhou, Yiyang Liu, Yinxi Zou, Haoyao Guo, Yuelun Zhang, Mengtao Li, Mingli Li, Yan Xu, Weihai Xu
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Abstract

Background and purpose: Autoimmune rheumatic diseases (AIRD) can cause intracranial artery stenosis (ICAS) and lead to stroke. This study aimed to characterize patients with ICAS associated with AIRD.

Materials and methods: Using data from a high-resolution MR imaging database, we retrospectively reviewed patients with AIRD with ICAS. Stratification into vasculitis, atherosclerosis, and mixed atherovasculitis subtypes was based on imaging findings, followed by a comparative analysis of clinical characteristics and outcomes across these subgroups.

Results: Among 139 patients (mean, 45.1 [SD, 17.3] years; 64.7% women), 56 (40.3%) were identified with vasculitis; 57 (41.0%), with atherosclerosis; and 26 (18.7%), with mixed atherovasculitis. The average interval from AIRD onset to high-resolution MRI was 5 years. Patients with vasculitis presented at a younger age of AIRD onset (mean, 34.5 [SD, 19.4] years), nearly 10 years earlier than other groups (P = .010), with a higher artery occlusion incidence (44.6% versus 21.1% and 26.9%, P = .021). Patients with atherosclerosis showed the highest cardiovascular risk factor prevalence (73.7% versus 48.2% and 61.5%, P = .021) but fewer intracranial artery wall enhancement instances (63.2% versus 100% in others, P < .001). The mixed atherovasculitis group, predominantly men (69.2% versus 30.4% and 24.6%, P < .001), exhibited the most arterial involvement (5 arteries per person versus 3 and 2, P = .001). Over an average 21-month follow-up, 23 (17.0%) patients experienced stroke events and 8 (5.9%) died, with the mixed atherovasculitis group facing the highest risk of stroke events (32.0%) and the highest mortality (12.0%).

Conclusions: Intracranial arteries are injured and lead to heterogeneous disease courses when exposed to AIRD and cardiovascular risk factors. While atherosclerosis acceleration is common, vasculitis may further contribute to the early development of occlusion and multiple artery involvement. Varied intracranial arteriopathies may result in different outcomes.

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自身免疫性风湿病颅内动脉狭窄的病因--一项观察性高分辨率磁共振成像研究。
背景和目的:自身免疫性风湿病(AIRD)可导致颅内动脉狭窄(ICAS)并引发脑卒中。本研究旨在描述与 AIRD 相关的 ICAS 患者的特征:利用高分辨率磁共振成像(HRMRI)数据库中的数据,我们对患有 ICAS 的 AIRD 患者进行了回顾性研究。根据成像结果将患者分为脉管炎、动脉粥样硬化和混合动脉粥样硬化-脉管炎亚型,然后对这些亚型的临床特征和预后进行比较分析:在139名患者(45.1±17.3岁;64.7%为女性)中,56人(40.3%)被确定为脉管炎患者,57人(41.0%)为动脉粥样硬化患者,26人(18.7%)为混合型动脉粥样硬化-脉管炎患者。从 AIRD 发病到进行 HRMRI 检查的平均间隔时间为 5 年。血管炎患者的 AIRD 发病年龄较小(34.5±19.4 岁),比其他组早近 10 年(P=0.010),动脉闭塞发生率较高(44.6% 对 21.1% 和 26.9%,P=0.021)。动脉粥样硬化患者的心血管危险因素发生率最高(73.7% vs. 48.2% 和 61.5%,P=0.021),但颅内动脉壁强化发生率较低(63.2% vs. 100%,PC结论:颅内动脉会受到损伤,并在暴露于空气吸入性动脉粥样硬化和心血管危险因素时导致不同的病程。虽然动脉粥样硬化加速很常见,但血管炎可能会进一步导致早期闭塞和多支动脉受累。不同的颅内动脉病变可能导致不同的结果:缩写:ICAS = 颅内动脉狭窄;AIRD = 自身免疫性风湿病;HRMRI = 高分辨率磁共振成像。
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