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Effect of tobacco use on disease activity and DMT discontinuation in multiple sclerosis patients treated with dimethyl fumarate or fingolimod
BACKGROUND: Tobacco exposure is a modifiable risk factor for multiple sclerosis (MS). Studies evaluating the relationship between tobacco, disease activity, and disease modifying therapy (DMT) persistence yielded conflicting results. We sought to address this issue with data from clinical practice....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557793/ https://www.ncbi.nlm.nih.gov/pubmed/33110616 http://dx.doi.org/10.1177/2055217320959815 |
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author | Hersh, Carrie M Harris, Haleigh Ayers, Malissa Conway, Devon |
author_facet | Hersh, Carrie M Harris, Haleigh Ayers, Malissa Conway, Devon |
author_sort | Hersh, Carrie M |
collection | PubMed |
description | BACKGROUND: Tobacco exposure is a modifiable risk factor for multiple sclerosis (MS). Studies evaluating the relationship between tobacco, disease activity, and disease modifying therapy (DMT) persistence yielded conflicting results. We sought to address this issue with data from clinical practice. OBJECTIVE: To compare 24-month disease outcomes in tobacco versus non-tobacco users treated with dimethyl fumarate (DMF) or fingolimod (FTY) in clinical practice. METHODS: We retrospectively identified 659 MS patients treated with DMF or FTY, stratified by patient-reported tobacco use. DMT discontinuation and measures of disease activity at 24 months were assessed using propensity score (PS) weighting. Outcome estimates were calculated as tobacco vs non-tobacco use. RESULTS: 164 tobacco users (DMF n = 101; FTY n = 63) and 495 non-tobacco users (DMF n = 294; FTY n = 201) were identified. Tobacco (39.4%) and non-tobacco (34.4%) users were equally likely to discontinue DMT (OR = 1.17, 95% CI 0.79, 1.75), but tobacco users discontinued therapy earlier (HR = 1.53, 95% CI 1.06, 2.43). There were no differences in ARR (rate ratio = 1.39, 95% CI 0.97, 1.96). However, tobacco users had decreased odds of NEDA-2 (OR = 0.61, 95% CI 0.44, 0.83). CONCLUSION: Our findings suggest that tobacco is a negative risk factor for inflammatory disease activity and earlier DMF and FTY discontinuation. |
format | Online Article Text |
id | pubmed-7557793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75577932020-10-26 Effect of tobacco use on disease activity and DMT discontinuation in multiple sclerosis patients treated with dimethyl fumarate or fingolimod Hersh, Carrie M Harris, Haleigh Ayers, Malissa Conway, Devon Mult Scler J Exp Transl Clin Original Article BACKGROUND: Tobacco exposure is a modifiable risk factor for multiple sclerosis (MS). Studies evaluating the relationship between tobacco, disease activity, and disease modifying therapy (DMT) persistence yielded conflicting results. We sought to address this issue with data from clinical practice. OBJECTIVE: To compare 24-month disease outcomes in tobacco versus non-tobacco users treated with dimethyl fumarate (DMF) or fingolimod (FTY) in clinical practice. METHODS: We retrospectively identified 659 MS patients treated with DMF or FTY, stratified by patient-reported tobacco use. DMT discontinuation and measures of disease activity at 24 months were assessed using propensity score (PS) weighting. Outcome estimates were calculated as tobacco vs non-tobacco use. RESULTS: 164 tobacco users (DMF n = 101; FTY n = 63) and 495 non-tobacco users (DMF n = 294; FTY n = 201) were identified. Tobacco (39.4%) and non-tobacco (34.4%) users were equally likely to discontinue DMT (OR = 1.17, 95% CI 0.79, 1.75), but tobacco users discontinued therapy earlier (HR = 1.53, 95% CI 1.06, 2.43). There were no differences in ARR (rate ratio = 1.39, 95% CI 0.97, 1.96). However, tobacco users had decreased odds of NEDA-2 (OR = 0.61, 95% CI 0.44, 0.83). CONCLUSION: Our findings suggest that tobacco is a negative risk factor for inflammatory disease activity and earlier DMF and FTY discontinuation. SAGE Publications 2020-10-13 /pmc/articles/PMC7557793/ /pubmed/33110616 http://dx.doi.org/10.1177/2055217320959815 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Hersh, Carrie M Harris, Haleigh Ayers, Malissa Conway, Devon Effect of tobacco use on disease activity and DMT discontinuation in multiple sclerosis patients treated with dimethyl fumarate or fingolimod |
title | Effect of tobacco use on disease activity and DMT discontinuation in
multiple sclerosis patients treated with dimethyl fumarate or
fingolimod |
title_full | Effect of tobacco use on disease activity and DMT discontinuation in
multiple sclerosis patients treated with dimethyl fumarate or
fingolimod |
title_fullStr | Effect of tobacco use on disease activity and DMT discontinuation in
multiple sclerosis patients treated with dimethyl fumarate or
fingolimod |
title_full_unstemmed | Effect of tobacco use on disease activity and DMT discontinuation in
multiple sclerosis patients treated with dimethyl fumarate or
fingolimod |
title_short | Effect of tobacco use on disease activity and DMT discontinuation in
multiple sclerosis patients treated with dimethyl fumarate or
fingolimod |
title_sort | effect of tobacco use on disease activity and dmt discontinuation in
multiple sclerosis patients treated with dimethyl fumarate or
fingolimod |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557793/ https://www.ncbi.nlm.nih.gov/pubmed/33110616 http://dx.doi.org/10.1177/2055217320959815 |
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