Published in:
Open Access
01-12-2013 | Research article
Adverse events during the titration phase of interferon-beta in remitting-relapsing multiple sclerosis are not predicted by body mass index nor by pharmacodynamic biomarkers
Authors:
Delicias Muñoz, Antonio Escartín, Dolores Dapena, Francisco Coret, Dionisio Fernández-Uría, Domingo Pérez, Bonaventura Casanova, Cristina Guijarro-Castro, Elvira Munteis, María del-Campo Amigo, Robustiano Pego, Carmen Calles, César García-Rey, Nuria Monsalve, David Sánchez-Matienzo
Published in:
BMC Neurology
|
Issue 1/2013
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Abstract
Background
This study aimed to correlate body mass index or biomarkers with the frequency of common adverse events (AEs) with subcutaneous IFN β-1a during treatment titration in patients with relapsing-remitting multiple sclerosis previously naïve to IFN β.
Methods
Eighty-four patients (66.3% females) were followed up during 8 weeks, 25.3% were overweight and 14.5% were obese.
Results
Biomarkers steadily increased during all study period by 45.3% for β2-microglobulin, 262.8% for olygoadenylate synthetase-1, and 92.8% for neopterin. Overall AE reporting did not vary with the dose or treatment duration.
Conclusions
BMI was not predictive of increased risk for AEs. Biomarkers did not discriminate on the frequency of any AE either.