免疫球蛋白A缺乏症的临床表现:系统回顾和荟萃分析。

Ahmad Vosughimotlagh, Seyed Erfan Rasouli, Hosein Rafiemanesh, Molood Safarirad, Niusha Sharifinejad, Atossa Madanipour, Maria Marluce Dos Santos Vilela, Edyta Heropolitańska-Pliszka, Gholamreza Azizi
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引用次数: 0

摘要

目的:免疫球蛋白A缺乏症(IgAD)是一种常见的疾病,具有未知的遗传缺陷,其特征是IgA减少或缺失,其他同型正常、正常亚类和特异性抗体。患有这种疾病的患者表现出一系列的临床表现,包括感染、自身免疫性疾病、恶性肿瘤和过敏性疾病。目前的研究旨在评估其流行程度并对其进行分类。方法:检索PubMed、Web of Science和Scopus数据库,以标准关键词查找最早可查日期至2022年1月的符合条件的研究。使用随机效应模型计算临床表现患病率和相应的95%置信区间的汇总估计值。结果:临床表现以感染为主(64.8%),其次为变应性疾病(26.16%)和自身免疫性疾病(22.0%)。选择性IgA缺乏症患者是本研究中最大的IgAD群体,乳糜泻(6.57%)、炎症性肠病(4.01%)和类风湿关节炎(3.80%)是最常见的自身免疫。以呼吸道感染、真菌感染和胃肠道感染为主,分别占50.74%、18.48%和15.79%。此外,哮喘、变应性鼻炎和变应性结膜炎的总患病率分别为19.06%、15.46%和11.68%,是最普遍的变应性疾病。结论:我们的研究结果表明,除了未确诊的IgAD患者外,IgAD患者具有广泛的临床表现。感染、过敏和自身免疫是最常见的临床表现。同时存在IgA和IgG亚型缺乏可能与感染易感性增加有关。考虑到随访期间出现新的临床并发症的可能性,应定期检查IgAD患者的评估情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical manifestation for immunoglobulin A deficiency: a systematic review and meta-analysis.

Clinical manifestation for immunoglobulin A deficiency: a systematic review and meta-analysis.

Clinical manifestation for immunoglobulin A deficiency: a systematic review and meta-analysis.

Clinical manifestation for immunoglobulin A deficiency: a systematic review and meta-analysis.

Objectives: Immunoglobulin A deficiency (IgAD) is a common disease with an unknown genetic defect, characterized by the decreased or absent IgA with other isotypes normal, normal subclasses, and specific antibodies. Patients with this disorder represent a spectrum of clinical manifestations including infections, autoimmune disorders, malignancy, and allergic diseases. The current study aimed to evaluate their prevalence and categorized them.

Methods: We searched PubMed, Web of Science, and Scopus databases to find eligible studies from the earliest available date to January 2022 with standard keywords. Pooled estimates of clinical manifestations prevalence and the corresponding 95% confidence intervals were calculated using random-effects models.

Results: The most prevalent clinical manifestations belonged to infection (64.8%) followed by allergic diseases (26.16%) and autoimmunity (22.0%), respectively. In selective IgA deficiency patients as the largest group of IgAD in current study, celiac disease (6.57%), Inflammatory bowel disease (4.01%), and rheumatoid arthritis (3.80%) were the most prevalent autoimmunity. Meanwhile, the most frequent infection was respiratory tract infection, fungal infection, and gastrointestinal infection at 50.74%, 18.48%, and 15.79%, respectively. In addition, the pooled prevalence of asthma, allergic rhinitis, and allergic conjunctivitis were 19.06%, 15.46%, and 11.68%, respectively which were reported as the most widespread allergic diseases.

Conclusions: Our results showed that apart from undiagnosed IgAD patients, IgAD patients represent a wide range of clinical manifestations. Infection, allergy, and autoimmunity are the most common clinical manifestations. The concurrent presence of IgA and IgG subtypes deficiency could be associated with increased susceptibility to infection. Considering the probability of developing new clinical complications during follow-up, periodic assessments of IgAD patients should be inspected.

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