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Erschienen in: Metabolic Brain Disease 3/2018

18.12.2017 | Short Communication

Cardiovascular profile improvement during Natalizumab treatment

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

Erschienen in: Metabolic Brain Disease | Ausgabe 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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Metadaten
Titel
Cardiovascular profile improvement during Natalizumab treatment
verfasst von
Marcello Moccia
Roberto Albero
Roberta Lanzillo
Francesco Saccà
Anna De Rosa
Cinzia Valeria Russo
Antonio Carotenuto
Raffaele Palladino
Vincenzo Brescia Morra
Publikationsdatum
18.12.2017
Verlag
Springer US
Erschienen in
Metabolic Brain Disease / Ausgabe 3/2018
Print ISSN: 0885-7490
Elektronische ISSN: 1573-7365
DOI
https://doi.org/10.1007/s11011-017-0169-z

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