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Influence of Interferon beta treatment on quality of life in multiple sclerosis patients

BACKGROUND: Interferon-beta (IFN-β) shows beneficial effect on the course of multiple sclerosis (MS), nevertheless its route and frequency of administration and side effects might impact negatively the quality of life (QoL) of MS patients. The objective of this study was to evaluate the influence of...

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Autores principales: Simone, Isabella Laura, Ceccarelli, Antonia, Tortorella, Carla, Bellacosa, Alessandra, Pellegrini, Fabio, Plasmati, Immacolata, De Caro, Maria Fara, Lopez, Mariangela, Girolamo, Francesco, Livrea, Paolo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1716163/
https://www.ncbi.nlm.nih.gov/pubmed/17163989
http://dx.doi.org/10.1186/1477-7525-4-96
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author Simone, Isabella Laura
Ceccarelli, Antonia
Tortorella, Carla
Bellacosa, Alessandra
Pellegrini, Fabio
Plasmati, Immacolata
De Caro, Maria Fara
Lopez, Mariangela
Girolamo, Francesco
Livrea, Paolo
author_facet Simone, Isabella Laura
Ceccarelli, Antonia
Tortorella, Carla
Bellacosa, Alessandra
Pellegrini, Fabio
Plasmati, Immacolata
De Caro, Maria Fara
Lopez, Mariangela
Girolamo, Francesco
Livrea, Paolo
author_sort Simone, Isabella Laura
collection PubMed
description BACKGROUND: Interferon-beta (IFN-β) shows beneficial effect on the course of multiple sclerosis (MS), nevertheless its route and frequency of administration and side effects might impact negatively the quality of life (QoL) of MS patients. The objective of this study was to evaluate the influence of IFN-β on QoL in MS patients. METHODS: Seventy-seven disease modifying treatment (DMT) free and 41 IFN-β treated MS patients were evaluated. QoL, assessed by MSQoL-54, was related to IFN-β treatment and to clinical and demographic parameters at baseline and after two years. Multivariate hierarchical linear model for repeated measurements was used. RESULTS: Treated patients showed a younger age, a lower disease duration and a higher relapse rate in the two years preceding study entry. At inclusion time treated and untreated patients did not differ in relapse rate, expanded disability status scale (EDSS), fatigue, depression, physical and mental QoL. IFN-β did not influence QoL at inclusion time, but when QoL was evaluated after two years, treatment negatively affected mental QoL. Depression and fatigue negatively influenced physical and mental QoL both at baseline and after two years. EDSS correlated with a poor physical QoL only at baseline. CONCLUSION: IFN-β had a negative impact on QoL over the time in MS patients, influencing mainly mental QoL. The impairment of QoL in MS was strongly associated with increasing fatigue and depression, whereas clinical disability had a minor unfavourable role.
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spelling pubmed-17161632006-12-22 Influence of Interferon beta treatment on quality of life in multiple sclerosis patients Simone, Isabella Laura Ceccarelli, Antonia Tortorella, Carla Bellacosa, Alessandra Pellegrini, Fabio Plasmati, Immacolata De Caro, Maria Fara Lopez, Mariangela Girolamo, Francesco Livrea, Paolo Health Qual Life Outcomes Research BACKGROUND: Interferon-beta (IFN-β) shows beneficial effect on the course of multiple sclerosis (MS), nevertheless its route and frequency of administration and side effects might impact negatively the quality of life (QoL) of MS patients. The objective of this study was to evaluate the influence of IFN-β on QoL in MS patients. METHODS: Seventy-seven disease modifying treatment (DMT) free and 41 IFN-β treated MS patients were evaluated. QoL, assessed by MSQoL-54, was related to IFN-β treatment and to clinical and demographic parameters at baseline and after two years. Multivariate hierarchical linear model for repeated measurements was used. RESULTS: Treated patients showed a younger age, a lower disease duration and a higher relapse rate in the two years preceding study entry. At inclusion time treated and untreated patients did not differ in relapse rate, expanded disability status scale (EDSS), fatigue, depression, physical and mental QoL. IFN-β did not influence QoL at inclusion time, but when QoL was evaluated after two years, treatment negatively affected mental QoL. Depression and fatigue negatively influenced physical and mental QoL both at baseline and after two years. EDSS correlated with a poor physical QoL only at baseline. CONCLUSION: IFN-β had a negative impact on QoL over the time in MS patients, influencing mainly mental QoL. The impairment of QoL in MS was strongly associated with increasing fatigue and depression, whereas clinical disability had a minor unfavourable role. BioMed Central 2006-12-12 /pmc/articles/PMC1716163/ /pubmed/17163989 http://dx.doi.org/10.1186/1477-7525-4-96 Text en Copyright © 2006 Simone et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Simone, Isabella Laura
Ceccarelli, Antonia
Tortorella, Carla
Bellacosa, Alessandra
Pellegrini, Fabio
Plasmati, Immacolata
De Caro, Maria Fara
Lopez, Mariangela
Girolamo, Francesco
Livrea, Paolo
Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
title Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
title_full Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
title_fullStr Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
title_full_unstemmed Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
title_short Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
title_sort influence of interferon beta treatment on quality of life in multiple sclerosis patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1716163/
https://www.ncbi.nlm.nih.gov/pubmed/17163989
http://dx.doi.org/10.1186/1477-7525-4-96
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