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Association between Intracranial Arterial Dolichoectasia and Cerebral Small Vessel Disease and Its Underlying Mechanisms

机译:颅内动脉回肠毛细血管扩张与脑小血管疾病的关系及其潜在机制

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摘要

Intracranial arterial dolichoectasia (IADE), also known as dilatative arteriopathy of the brain vessels, refers to an increase in the length and diameter of at least one intracranial artery, and accounts for approximately 12% of all patients with stroke. However, the association of IADE with stroke is usually unclear. Cerebral small vessel disease (CSVD) is characterized by pathological changes in the small vessels. Clinically, patients with CSVD can be asymptomatic or present with stroke or cognitive decline. In the past 20 years, a series of studies have strongly promoted an understanding of the association between IADE and CSVD from clinical and pathological perspectives. It has been proposed that IADE and CSVD may be attributed to abnormal vascular remodeling driven by an abnormal matrix metalloproteinase/tissue inhibitor of metalloproteinase pathway. Also, IAD-Erelated hemodynamic changes may result in initiation or progression of CSVD. Additionally, genetic factors are implicated in the pathogenesis of IADE and CSVD. Patients with Fabry’s disease and late-onset Pompe’s disease are prone to developing concomitant IADE and CSVD, and patients with collagen IV alpha 1 or 2 gene ( / ) and forkhead box C1 ( ) variants present with IADE and CSVD. Race, strain, familial status, and vascular risk factors may be involved in the pathogenesis of IADE and CSVD. As well, experiments in mice have pointed to genetic strain as a predisposing factor for IADE and CSVD. However, there have been few direct genetic studies aimed towards determining the association between IADE and CSVD. In the future, more clinical and basic research studies are needed to elucidate the causal relationship between IADE and CSVD and the related molecular and genetic mechanisms.
机译:颅内动脉多发性胆管扩张症(IADE),也称为脑血管扩张性动脉病,是指至少一条颅内动脉的长度和直径增加,约占所有中风患者的12%。但是,IADE与卒中的关系通常尚不清楚。脑小血管疾病(CSVD)的特征是小血管的病理变化。在临床上,CSVD患者可以是无症状的,也可以是中风或认知功能减退的患者。在过去的20年中,一系列研究从临床和病理学的角度极大地促进了对IADE和CSVD之间关联的理解。有人提出IADE和CSVD可能归因于异常基质金属蛋白酶/金属蛋白酶途径的组织抑制剂驱动的异常血管重塑。同样,IAD相关的血液动力学变化可能导致CSVD的发生或发展。此外,遗传因素与IADE和CSVD的发病机制有关。患有法布里(Fabry)病和迟发性庞贝氏病(Pompe's disease)的患者容易发生并发IADE和CSVD,并且IADE和CSVD存在具有胶原IVα1或2基因(/)和叉头盒C1()变体的患者。种族,劳损,家族状态和血管危险因素可能与IADE和CSVD的发病机制有关。同样,在小鼠中的实验也指出,遗传应变是IADE和CSVD的诱因。但是,很少有直接的遗传学研究旨在确定IADE和CSVD之间的关联。将来,需要更多的临床和基础研究来阐明IADE和CSVD之间的因果关系以及相关的分子和遗传机制。

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