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. 2019 Mar 29:15:20.
doi: 10.1186/s13223-019-0331-8. eCollection 2019.

Variability in total serum IgE over 1 year in severe asthmatics

Affiliations

Variability in total serum IgE over 1 year in severe asthmatics

Renaud Louis et al. Allergy Asthma Clin Immunol. .

Abstract

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 (sIgEtot) in asthmatics remains poorly documented.

Methods: In this prospective study, sIgEtot levels were measured over 1 year at 7 time points in 41 severe asthmatics treated with high-dose of inhaled corticosteroids and long-acting β2 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 sIgEtot 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 (ACQ6). The sIgEtot variability and factors predictive for this variability were studied, as well as ACQ6 outcomes.

Results: The variation in sIgEtot 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 sIgEtot subgroups, respectively. The residual within-patient variability was therefore limited. In 10/41 patients, sIgEtot 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 sIgEtot and ACQ6 score over all time points (r = 0.15, p = 0.02), but sIgEtot failed to associate with severe exacerbation. sIgEtot 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 sIgEtot levels was observed over 1 year as opposed to marked between-subject variability. sIgEtot decreases with age. Variation in sIgEtot weakly associates with asthma control but not with exacerbation.

Keywords: Asthma; IgE; Variability.

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Conflict of interest statement

GB, RL, AM, OM and CP are members of an Advisory Board of Novartis Pharma, Belgium. IA and KD work for Matrix45, LLC. By company policy employees are prohibited from owning equity in or perform services independently for sponsor organizations. Matrix45 provides similar services to other biopharmaceutical on a non-exclusivity basis. SG, AP, JVS and SV are employees of Novartis Pharma, Belgium.

Figures

Fig. 1
Fig. 1
The 12-month variability in sIgEtot in severe asthmatic patients stratified by sIgEtot at baseline (low, intermediate and high). The 12-month variability in sIgEtot was evaluated in 41 patients divided post hoc in three strata based on sIgEtot at baseline: < 76 IU/mL (n = 10) (a); 76–700 IU/mL (n = 20) (c) and > 700 IU/mL (n = 11) (d). One outliner patient from the low sIgEtot group is shown separately (b). The gray zone indicates the 76–700 IU/mL region (intermediate group) to allow for the identification of patients whose sIgEtot reached the level of a different group during the study period
Fig. 2
Fig. 2
Variation in sIgEtot and asthma control in severe asthmatic patients (n = 41) according to the seasons. Data from the 6 follow-up visits are shown according to the month of the visit (the baseline data are not included). In these graphics, the geometric mean sIgEtot with standard deviation (SD) (a) and the geometric mean six-item Juniper Asthma Control Questionnaire (ACQ6) score with SD (b) are given

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