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Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide
BACKGROUND: Teriflunomide 14 mg significantly reduced brain volume loss (BVL) and confirmed disability worsening (CDW) compared with placebo in the TEMSO core study. OBJECTIVE: To investigate the relationship between BVL from Baseline to Year 2 in the TEMSO core study and long-term CDW (Year 7) in t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493202/ https://www.ncbi.nlm.nih.gov/pubmed/31198103 http://dx.doi.org/10.1177/1352458519855722 |
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author | Sprenger, Till Kappos, Ludwig Radue, Ernst-Wilhelm Gaetano, Laura Mueller-Lenke, Nicole Wuerfel, Jens Poole, Elizabeth M Cavalier, Steven |
author_facet | Sprenger, Till Kappos, Ludwig Radue, Ernst-Wilhelm Gaetano, Laura Mueller-Lenke, Nicole Wuerfel, Jens Poole, Elizabeth M Cavalier, Steven |
author_sort | Sprenger, Till |
collection | PubMed |
description | BACKGROUND: Teriflunomide 14 mg significantly reduced brain volume loss (BVL) and confirmed disability worsening (CDW) compared with placebo in the TEMSO core study. OBJECTIVE: To investigate the relationship between BVL from Baseline to Year 2 in the TEMSO core study and long-term CDW (Year 7) in the TEMSO long-term extension (NCT00803049). METHODS: Structural Image Evaluation using Normalization of Atrophy determined BVL. Long-term CDW was assessed by Expanded Disability Status Scale confirmed for 12 and 24 weeks. An additional analysis evaluated the relative contribution of BVL (Year 2) and other outcomes as potential mediators of the effect of teriflunomide 14 mg on 12-week CDW. RESULTS: Patients with the least BVL were significantly less likely to have 12- and 24-week CDW at Year 7 compared with patients with the most BVL. A mediation analysis revealed that BVL (Year 2) explained 51.3% of the treatment effect on CDW; new or enlarging T(2w) lesions over 2 years explained 30.8%, and relapses in the first 2 years explained 38.5%. CONCLUSIONS: These results highlight the potential predictive value of BVL earlier in the disease course on long-term disability outcomes. The mediation analysis suggests that teriflunomide may prevent disability worsening largely through its effects on BVL. |
format | Online Article Text |
id | pubmed-7493202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-74932022020-09-24 Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide Sprenger, Till Kappos, Ludwig Radue, Ernst-Wilhelm Gaetano, Laura Mueller-Lenke, Nicole Wuerfel, Jens Poole, Elizabeth M Cavalier, Steven Mult Scler Original Research Papers BACKGROUND: Teriflunomide 14 mg significantly reduced brain volume loss (BVL) and confirmed disability worsening (CDW) compared with placebo in the TEMSO core study. OBJECTIVE: To investigate the relationship between BVL from Baseline to Year 2 in the TEMSO core study and long-term CDW (Year 7) in the TEMSO long-term extension (NCT00803049). METHODS: Structural Image Evaluation using Normalization of Atrophy determined BVL. Long-term CDW was assessed by Expanded Disability Status Scale confirmed for 12 and 24 weeks. An additional analysis evaluated the relative contribution of BVL (Year 2) and other outcomes as potential mediators of the effect of teriflunomide 14 mg on 12-week CDW. RESULTS: Patients with the least BVL were significantly less likely to have 12- and 24-week CDW at Year 7 compared with patients with the most BVL. A mediation analysis revealed that BVL (Year 2) explained 51.3% of the treatment effect on CDW; new or enlarging T(2w) lesions over 2 years explained 30.8%, and relapses in the first 2 years explained 38.5%. CONCLUSIONS: These results highlight the potential predictive value of BVL earlier in the disease course on long-term disability outcomes. The mediation analysis suggests that teriflunomide may prevent disability worsening largely through its effects on BVL. SAGE Publications 2019-06-14 2020-09 /pmc/articles/PMC7493202/ /pubmed/31198103 http://dx.doi.org/10.1177/1352458519855722 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.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 Research Papers Sprenger, Till Kappos, Ludwig Radue, Ernst-Wilhelm Gaetano, Laura Mueller-Lenke, Nicole Wuerfel, Jens Poole, Elizabeth M Cavalier, Steven Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
title | Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
title_full | Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
title_fullStr | Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
title_full_unstemmed | Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
title_short | Association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
title_sort | association of brain volume loss and long-term disability outcomes in patients with multiple sclerosis treated with teriflunomide |
topic | Original Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493202/ https://www.ncbi.nlm.nih.gov/pubmed/31198103 http://dx.doi.org/10.1177/1352458519855722 |
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