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

• Review
• Open Access

Ahmad Vosughimotlagh, 

Seyed Erfan Rasouli, 

Hosein Rafiemanesh, 

Molood Safarirad, 

Niusha Sharifinejad, 

Atossa Madanipour, 

Maria Marluce Dos Santos Vilela, 

Edyta Heropolitańska-Pliszka & 

Gholamreza Azizi 

Allergy, Asthma & Clinical Immunology volume 19, Article number: 75 (2023) 

• details

Abstract

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 forest plot and pooled prevalence of the infection
in SIgAD

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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