Oral Contraceptives Interact with Adiposity-Associated Markers in Patients with Multiple Sclerosis

Author:

Ferret-Sena Véronique1,Ramos Catarina1,Cascais Maria João2,Capela Carlos34,Sena Armando1ORCID

Affiliation:

1. Egas Moniz Center for Interdisciplinary Research (CiiEM), Egas Moniz School of Health & Science, Caparica, 2829-511 Almada, Portugal

2. Nutritional Biochemistry, NOVA Medical School, Universidade Nova de Lisboa, 1150-199 Lisbon, Portugal

3. Centro de Responsabilidade Integrado de Esclerose Múltipla, Hospital Santo António dos Capuchos, Centro Hospitalar Universitário Lisboa Central, EPE, 1169-050 Lisbon, Portugal

4. Centro Clínico Académico de Lisboa, 1159-056 Lisbon, Portugal

Abstract

Growing evidence suggests the involvement of adipose tissue in modulating the clinical course of relapsing–remitting multiple sclerosis (RRMS). This study aimed to investigate whether the intake of combined oral contraceptives (COCs) affects body weight and leptin and adiponectin (APN) blood levels in these patients. Clinical data from 62 women (M = 33.23 year) were recorded prior to the initiation of disease-modifying therapy. Patients who were taking COCs at the time of experiencing the first symptoms of disease (COC user) were compared with those who never used these formulations or stopped taking them before disease onset (COC non-user). Bivariate Pearson’s correlations and hierarchical multiple linear regressions analysis were conducted. Normalized APN levels were lower in the COC-using patients (p = 0.013). Negative correlations between waist circumference and normalized APN (p = 0.001) were observed only in the COC non-user patients. A longer duration of COC intake was associated with increased body mass index and waist circumference (p = 0.003). Normalized APN predicted the MS Severity Score (MSSS) (p = 0.020), but this correlation was lost in the COC user patients. After adjusting for confounders, only age (p = 0.027) and, later, disease onset (p = 0.014) were correlated with the MSSS. Larger and prospective studies are needed to investigate the interactions of sex steroids with adipose metabolism in modulating disease progression.

Funder

CiiEM

Publisher

MDPI AG

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