Audiovestibular Dysfunction Related to Anti-Phospholipid Syndrome: A Systematic Review.

IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Jiann-Jy Chen, Chih-Wei Hsu, Yen-Wen Chen, Tien-Yu Chen, Bing-Yan Zeng, Ping-Tao Tseng
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引用次数: 0

Abstract

Background: Anti-phospholipid syndrome (APS) has emerged as a significant issue in autoimmune diseases over recent decades. Its hallmark feature is thromboembolic events, potentially affecting any vascularized area including the microcirculation of the inner ear. Since the first case report of APS-related audiovestibular dysfunction described in 1993, numerous reports have explored the association between APS-related antibodies and audiovestibular dysfunction. These studies indicate a higher prevalence of APS-related antibodies in patients with sensorineural hearing loss compared to healthy controls. Unlike other idiopathic hearing loss disorders, audiovestibular dysfunction associated with APS may respond to appropriate treatments, highlighting the importance of timely recognition by clinicians to potentially achieve favorable outcomes. Therefore, this systematic review aims to consolidate current evidence on the characteristics, pathophysiology, assessment, and management of audiovestibular dysfunction linked to APS. Methods: This systematic review utilized electronic searches of the PubMed, Embase, ClinicalKey, Web of Science, and ScienceDirect online platforms. The initial search was performed on 27 January 2024, with the final update search completed on 20 June 2024. Results: Based on theoretical pathophysiology, anticoagulation emerges as a pivotal treatment strategy. Additionally, drawing from our preliminary data, we propose a modified protocol combining anticoagulants, steroids, and non-invasive brain stimulation to offer clinicians a novel therapeutic approach for managing these symptoms. Conclusions: Clinicians are encouraged to remain vigilant about the possibility of APS and its complex audiovestibular manifestations, as prompt intervention could stabilize audiovestibular function effectively.

与抗磷脂综合征有关的听觉功能障碍:系统综述。
背景:近几十年来,抗磷脂综合征(APS)已成为自身免疫性疾病中的一个重要问题。其标志性特征是血栓栓塞事件,可能影响任何血管区域,包括内耳的微循环。自 1993 年首例与 APS 相关的听觉前庭功能障碍病例报道以来,已有大量报道探讨了 APS 相关抗体与听觉前庭功能障碍之间的关联。这些研究表明,与健康对照组相比,感音神经性听力损失患者体内 APS 相关抗体的流行率更高。与其他特发性听力损失疾病不同,与APS相关的听觉前庭功能障碍可能会对适当的治疗产生反应,这凸显了临床医生及时识别的重要性,从而可能获得良好的治疗效果。因此,本系统综述旨在整合与 APS 相关的听觉前庭功能障碍的特征、病理生理学、评估和管理方面的现有证据。方法:本系统性综述利用 PubMed、Embase、ClinicalKey、Web of Science 和 ScienceDirect 在线平台进行电子检索。首次检索于 2024 年 1 月 27 日进行,最终更新检索于 2024 年 6 月 20 日完成。检索结果根据病理生理学理论,抗凝是一种关键的治疗策略。此外,根据我们的初步数据,我们提出了一种将抗凝剂、类固醇和非侵入性脑部刺激相结合的改良方案,为临床医生提供了一种新的治疗方法来控制这些症状。结论:我们鼓励临床医生对 APS 及其复杂的听觉前庭表现的可能性保持警惕,因为及时干预可有效稳定听觉前庭功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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