贝赫切特病:流行病学、分类标准和治疗方法。

IF 3.9 3区 医学 Q2 IMMUNOLOGY
Expert Review of Clinical Immunology Pub Date : 2024-12-01 Epub Date: 2024-08-11 DOI:10.1080/1744666X.2024.2388693
Alia Fazaa, Yasmine Makhlouf, Faiza Ben Massoud, Saoussen Miladi, Hiba Boussaa, Kmar Ouenniche, Leila Souebni, Selma Kassab, Selma Chekili, Kawther Ben Abdelghani, Ahmed Laatar
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引用次数: 0

摘要

简介白塞病(Behçet disease,BD)是一种病因不明的多系统炎症性疾病,据信是由遗传易感个体的感染和环境因素诱发的。由于 BD 的临床表现和地理分布多种多样,了解 BD 对全球健康的影响具有重要意义:本综述讨论了 BD 的流行病学,强调其发病率估计为每 10 万人口 10.3 例(95% CI,6.1, 17.7),在历史上与丝绸之路相关的地区发病率更高。研究探讨了诊断标准,重点关注临床表现,为医护人员识别和管理 BD 提供指导。此外,该综述还包括治疗策略,重点介绍了作为关键生物制剂的 TNF-α 抑制剂,以及 IL-1 抑制剂和 Ustekinumab 等新型药物,这些药物扩大了 BD 的治疗选择范围:我们的研究深入了解了BD治疗方法的演变情况,强调了TNF-α抑制剂等既有疗法的同时,新药的作用也在不断扩大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behçet disease: epidemiology, classification criteria and treatment modalities.

Introduction: Behçet disease (BD) is an inflammatory multisystem disorder of unknown etiology, believed to be triggered by infection and environmental factors in genetically predisposed individuals. The significance of understanding BD lies in its impact on global health due to its diverse clinical manifestations and geographical distribution.

Areas covered: This review discusses the epidemiology of BD, emphasizing its prevalence estimated at 10.3 (95% CI, 6.1, 17.7) per 100,000 population, with higher rates observed in regions historically linked to the Silk Route. The criteria for diagnosis are explored, focusing on clinical manifestations that guide healthcare professionals in identifying and managing BD. Additionally, the review encompasses treatment strategies, highlighting TNF-alpha inhibitors as pivotal biologics and newer agents like IL-1 inhibitors and Ustekinumab that broaden the therapeutic options for BD.

Expert opinion: Our work provides insights into the evolving landscape of treatments for BD, emphasizing the expanding role of newer agents alongside established therapies like TNF-alpha inhibitors.

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来源期刊
CiteScore
7.60
自引率
2.30%
发文量
221
审稿时长
6-12 weeks
期刊介绍: Expert Review of Clinical Immunology (ISSN 1744-666X) provides expert analysis and commentary regarding the performance of new therapeutic and diagnostic modalities in clinical immunology. Members of the International Editorial Advisory Panel of Expert Review of Clinical Immunology are the forefront of their area of expertise. This panel works with our dedicated editorial team to identify the most important and topical review themes and the corresponding expert(s) most appropriate to provide commentary and analysis. All articles are subject to rigorous peer-review, and the finished reviews provide an essential contribution to decision-making in clinical immunology. Articles focus on the following key areas: • Therapeutic overviews of specific immunologic disorders highlighting optimal therapy and prospects for new medicines • Performance and benefits of newly approved therapeutic agents • New diagnostic approaches • Screening and patient stratification • Pharmacoeconomic studies • New therapeutic indications for existing therapies • Adverse effects, occurrence and reduction • Prospects for medicines in late-stage trials approaching regulatory approval • Novel treatment strategies • Epidemiological studies • Commentary and comparison of treatment guidelines Topics include infection and immunity, inflammation, host defense mechanisms, congenital and acquired immunodeficiencies, anaphylaxis and allergy, systemic immune diseases, organ-specific inflammatory diseases, transplantation immunology, endocrinology and diabetes, cancer immunology, neuroimmunology and hematological diseases.
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