Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

European Society for Immunodeficiencies Registry Working Party

Research output: Contribution to journalArticlepeer-review

98 Scopus citations

Abstract

Background: Inborn errors of immunity (IEI) are rare diseases, which makes diagnosis a challenge. A better description of the initial presenting manifestations should improve awareness and avoid diagnostic delay. Although increased infection susceptibility is a well-known initial IEI manifestation, less is known about the frequency of other presenting manifestations. Objective: We sought to analyze age-related initial presenting manifestations of IEI including different IEI disease cohorts. Methods: We analyzed data on 16,486 patients of the European Society for Immunodeficiencies Registry. Patients with autoinflammatory diseases were excluded because of the limited number registered. Results: Overall, 68% of patients initially presented with infections only, 9% with immune dysregulation only, and 9% with a combination of both. Syndromic features were the presenting feature in 12%, 4% had laboratory abnormalities only, 1.5% were diagnosed because of family history only, and 0.8% presented with malignancy. Two-third of patients with IEI presented before the age of 6 years, but a quarter of patients developed initial symptoms only as adults. Immune dysregulation was most frequently recognized as an initial IEI manifestation between age 6 and 25 years, with male predominance until age 10 years, shifting to female predominance after age 40 years. Infections were most prevalent as a first manifestation in patients presenting after age 30 years. Conclusions: An exclusive focus on infection-centered warning signs would have missed around 25% of patients with IEI who initially present with other manifestations.

Original languageEnglish
Pages (from-to)1332-1341.e5
JournalJournal of Allergy and Clinical Immunology
Volume148
Issue number5
DOIs
StatePublished - Nov 2021

Funding

FundersFunder number
EURO-PADnet
European Society for Immunodeficiencies
Plasma Protein Therapeutics Association
Care-for-Rare Foundation
European CommissionHEALTH-F2-2008-201549
Bundesministerium für Bildung und Forschung01EO1303, 01GM0896, 01ZZ1801B, 01GM1517C, 01GM1111B

    Keywords

    • Primary immunodeficiency
    • autoimmune
    • immune dysregulation
    • inborn error of immunity
    • inflammatory
    • presenting symptom
    • registry
    • syndromic
    • warning signs

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