Predictive Factors for and Complications of Bronchiectasis in Common Variable Immunodeficiency Disorders.

Bronchiectasis Common variable immunodeficiency disorders Forced expiratory volume in one second Immunoglobulin M St George Respiratory Questionnaire

Journal

Journal of clinical immunology
ISSN: 1573-2592
Titre abrégé: J Clin Immunol
Pays: Netherlands
ID NLM: 8102137

Informations de publication

Date de publication:
04 2022
Historique:
received: 13 04 2021
accepted: 09 12 2021
pubmed: 12 1 2022
medline: 21 4 2022
entrez: 11 1 2022
Statut: ppublish

Résumé

Bronchiectasis is a frequent complication of common variable immunodeficiency disorders (CVID). In a cohort of patients with CVID, we sought to identify predictors of bronchiectasis. Secondly, we sought to describe the impact of bronchiectasis on lung function, infection risk, and quality of life. We conducted an observational cohort study of 110 patients with CVID and an available pulmonary computed tomography scan. The prevalence of bronchiectasis was 53%, with most of these patients (54%) having mild disease. Patients with bronchiectasis had lower median serum immunoglobulin (Ig) concentrations, especially long-term IgM (0 vs 0.25 g/l; p < 0.01) and pre-treatment IgG (1.3 vs 3.7 g/l; p < 0.01). CVID patients with bronchiectasis had worse forced expiratory volume in one second (2.10 vs 2.99 l; p < 0.01) and an annual decline in forced expiratory volume in one second of 25 ml/year (vs 8 ml/year in patients without bronchiectasis; p = 0.01). Patients with bronchiectasis also reported more annual respiratory tract infections (1.77 vs 1.25 infections/year, p = 0.04) and a poorer quality of life (26 vs 14 points in the St George's Respiratory Questionnaire; p = 0.02). Low serum immunoglobulin M concentration identifies patients at risk for bronchiectasis in CVID and may play a role in pathogenesis. Bronchiectasis is relevant because it is associated with frequent respiratory tract infections, poorer lung function, a greater rate of lung function decline, and a lower quality of life.

Identifiants

pubmed: 35015197
doi: 10.1007/s10875-022-01206-8
pii: 10.1007/s10875-022-01206-8
pmc: PMC9015976
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

572-581

Informations de copyright

© 2022. The Author(s).

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Auteurs

Johannes M Sperlich (JM)

Department of Clinical Immunology, Royal Free London NHS Foundation Trust, London, UK.
Center for Chronic Immunodeficiency, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.

Bodo Grimbacher (B)

Department of Clinical Immunology, Royal Free London NHS Foundation Trust, London, UK.
Center for Chronic Immunodeficiency, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.

Veronika Soetedjo (V)

Institute for Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.

Sarita Workman (S)

Department of Clinical Immunology, Royal Free London NHS Foundation Trust, London, UK.

Siobhan O Burns (SO)

Department of Clinical Immunology, Royal Free London NHS Foundation Trust, London, UK.
Institute of Immunity and Transplantation, University College London, London, UK.

David M Lowe (DM)

Department of Clinical Immunology, Royal Free London NHS Foundation Trust, London, UK.
Institute of Immunity and Transplantation, University College London, London, UK.

John R Hurst (JR)

UCL Respiratory, University College London, London, UK. j.hurst@ucl.ac.uk.

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