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Variability in total serum IgE over 1 year in severe asthmatics

BACKGROUND: Immunoglobulin E (IgE) is the treatment target of omalizumab, a monoclonal antibody indicated in the treatment of severe allergic asthma. Long-term variability of serum total IgE (sIgE(tot)) in asthmatics remains poorly documented. METHODS: In this prospective study, sIgE(tot) levels wer...

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Detalles Bibliográficos
Autores principales: Louis, Renaud, Pilette, Charles, Michel, Olivier, Michils, Alain, Brusselle, Guy, Poskin, Antoine, Van Schoor, Jan, Denhaerynck, Kris, Vancayzeele, Stefaan, Abraham, Ivo, Gurdain, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441212/
https://www.ncbi.nlm.nih.gov/pubmed/30976287
http://dx.doi.org/10.1186/s13223-019-0331-8
Descripción
Sumario:BACKGROUND: Immunoglobulin E (IgE) is the treatment target of omalizumab, a monoclonal antibody indicated in the treatment of severe allergic asthma. Long-term variability of serum total IgE (sIgE(tot)) in asthmatics remains poorly documented. METHODS: In this prospective study, sIgE(tot) levels were measured over 1 year at 7 time points in 41 severe asthmatics treated with high-dose of inhaled corticosteroids and long-acting β(2) agonists. 33 patients were atopic based on at least one positive RAST to common aeroallergens. Patients were divided into three groups according to their baseline sIgE(tot) level: low (< 76 IU/mL; n = 10), intermediate (76–700 IU/mL; n = 20) or high (> 700 IU/mL; n = 11). Patients also completed the six-item Juniper Asthma Control Questionnaire (ACQ(6)). The sIgE(tot) variability and factors predictive for this variability were studied, as well as ACQ(6) outcomes. RESULTS: The variation in sIgE(tot) level was mostly the consequence of between patient-variability, which represented 96%, 71% and 96% of the total variability in the low, intermediate and high sIgE(tot) subgroups, respectively. The residual within-patient variability was therefore limited. In 10/41 patients, sIgE(tot) levels increased or decreased, for at least one visit, beyond the predefined range of the subgroups to which they were assigned (< 76 IU/mL; 76–700 IU/mL; > 700 IU/mL). There was a significant but weak correlation between sIgE(tot) and ACQ(6) score over all time points (r = 0.15, p = 0.02), but sIgE(tot) failed to associate with severe exacerbation. sIgE(tot) decreased by 3% with any additional year of age for the whole group (p = 0.01) and increased by 5% per one unit of allergen exposure score in atopic patients (p = 0.002). CONCLUSION: In severe asthmatics, limited within-patient variability of sIgE(tot) levels was observed over 1 year as opposed to marked between-subject variability. sIgE(tot) decreases with age. Variation in sIgE(tot) weakly associates with asthma control but not with exacerbation.