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Published in: Metabolic Brain Disease 3/2018

01-06-2018 | Short Communication

Cardiovascular profile improvement during Natalizumab treatment

Authors: Marcello Moccia, Roberto Albero, Roberta Lanzillo, Francesco Saccà, Anna De Rosa, Cinzia Valeria Russo, Antonio Carotenuto, Raffaele Palladino, Vincenzo Brescia Morra

Published in: Metabolic Brain Disease | Issue 3/2018

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Abstract

Cardiovascular comorbidities are associated with the risk of MS progression. Thus, we aim to measure variations of cardiovascular risk factors during Natalizumab treatment and their possible clinical associations. Seventy-one relapsing-remitting MS patients treated with Natalizumab were followed-up during a 12.9 ± 6.2 months. Cardiovascular risk factors were recorded on first and last study visits: systolic blood pressure, uric acid, total cholesterol, LDL, HDL, and triglycerides. EDSS progression and relapse occurrence were recorded. At multilevel mixed-effects linear regression models, the population presented with a significant reduction of total cholesterol (Coeff = −7.340; 95%CI = −13.152--1.527; p = 0.013), and of HDL cholesterol (Coeff = −3.473; 95%CI = −6.333--0.613; p = 0.017), and a non-significant reduction of LDL cholesterol (Coeff = −1.872; 95%CI = −8.481–0.736; p = 0.053), and of triglycerides (Coeff = −8.815; 95%CI = −34.011–5.380; p = 0.094). Uric acid levels increased during the study period (Coeff = 0.159; 95%CI = 0.212–0.340; p = 0.038). No significant associations were found with clinical outcomes. Serum lipids decreased and anti-oxidant uric acid increased during Natalizumab treatment. These biomarkers need to be further explored in relation to clinical outcomes on larger cohorts with longer follow-ups.
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Metadata
Title
Cardiovascular profile improvement during Natalizumab treatment
Authors
Marcello Moccia
Roberto Albero
Roberta Lanzillo
Francesco Saccà
Anna De Rosa
Cinzia Valeria Russo
Antonio Carotenuto
Raffaele Palladino
Vincenzo Brescia Morra
Publication date
01-06-2018
Publisher
Springer US
Published in
Metabolic Brain Disease / Issue 3/2018
Print ISSN: 0885-7490
Electronic ISSN: 1573-7365
DOI
https://doi.org/10.1007/s11011-017-0169-z

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