Mohammed Maan Al-Salihi, Maryam Sabah Al-Jebur, Noor Mozahem, Kelly Nicol, Ahmed Abd Elazim, Ali Ayyad, Ram Saha
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引用次数: 0
摘要
背景:Loeys-Dietz综合征(LDS)是一种罕见的遗传性疾病,其特征是严重的全身性血管易损,具有复杂的神经血管表现,目前尚不完全清楚。本系统综述旨在全面绘制LDS的神经血管并发症谱,综合现有文献,确定与疾病严重程度相关的潜在遗传和表型相关性,并提出我们的病例报告,以说明现实世界的临床挑战和管理复杂性。方法:遵循PRISMA指南,对PubMed、Scopus、Web of Science和Cochrane Library从数据库建立到2025年3月进行了全面的文献检索。采用预先确定的纳入/排除标准对研究进行系统筛选。乔安娜布里格斯研究所关键评估清单被用于质量评估。结果:最终纳入25项研究,包括13项回顾性队列研究和12例病例报告。该综述揭示了LDS中显著的神经血管疾病负担。颅内动脉瘤患病率为19.4% ~ 30%,平均大小为3.6 mm。TGFBR1、TGFBR2和SMAD3基因突变与血管并发症密切相关。22.2%的患者记录有动脉夹层,神经血管事件跨越儿童到成人人群。我们的病例报告说明了该综合征复杂的多系统表现,显示双侧栓塞性梗死伴出血性成分。结论:本系统综述提供了LDS的神经血管并发症的全面特征,强调了对专门的、遗传特异性的风险分层和纵向监测的迫切需要。这些发现强调了基因突变与血管病理生理之间的复杂关系,强调了潜在的分子干预策略。
Neurovascular complications in Loeys-Dietz syndrome: a comprehensive systematic review and case report.
Background: Loeys-Dietz syndrome (LDS) is a rare genetic disorder characterized by profound systemic vascular vulnerability, with complex neurovascular manifestations that remain incompletely understood. This systematic review aimed to comprehensively map the spectrum of neurovascular complications in LDS, synthesize existing literature, identify potential genetic and phenotypic correlations contributing to disease severity, and present our case report to illustrate real-world clinical challenges and management complexities.
Methods: Following PRISMA guidelines, a comprehensive literature search was conducted across PubMed, Scopus, Web of Science, and Cochrane Library from database inception to March 2025. Studies were systematically screened using predefined inclusion/exclusion criteria. The Joanna Briggs Institute Critical Appraisal Checklists were employed for quality assessment.
Results: Twenty-five studies, including 13 retrospective cohort studies and 12 case reports, were ultimately included. The review revealed a significant neurovascular disease burden in LDS. Intracranial aneurysm prevalence ranged from 19.4 to 30%, with an average size of 3.6 mm. Genetic mutations in TGFBR1, TGFBR2, and SMAD3 genes were strongly associated with vascular complications. Arterial dissections were documented in 22.2% of patients, with neurovascular events spanning pediatric to adult populations. Our case report illustrated the syndrome's complex multisystemic manifestations, demonstrating bilateral embolic infarcts with hemorrhagic components.
Conclusions: This systematic review provides a comprehensive characterization of neurovascular complications in LDS, emphasizing the critical need for specialized, genetic-specific risk stratification and longitudinal monitoring. The findings underscore the complex relationship between genetic mutations and vascular pathophysiology, highlighting potential molecular intervention strategies.
期刊介绍:
Peer-reviewed and published quarterly, Acta Neurologica Belgicapresents original articles in the clinical and basic neurosciences, and also reports the proceedings and the abstracts of the scientific meetings of the different partner societies. The contents include commentaries, editorials, review articles, case reports, neuro-images of interest, book reviews and letters to the editor.
Acta Neurologica Belgica is the official journal of the following national societies:
Belgian Neurological Society
Belgian Society for Neuroscience
Belgian Society of Clinical Neurophysiology
Belgian Pediatric Neurology Society
Belgian Study Group of Multiple Sclerosis
Belgian Stroke Council
Belgian Headache Society
Belgian Study Group of Neuropathology