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Silent progression in disease activity–free relapsing multiple sclerosis
OBJECTIVE: Rates of worsening and evolution to secondary progressive multiple sclerosis (MS) may be substantially lower in actively treated patients compared to natural history studies from the pretreatment era. Nonetheless, in our recently reported prospective cohort, more than half of patients wit...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518998/ https://www.ncbi.nlm.nih.gov/pubmed/30851128 http://dx.doi.org/10.1002/ana.25463 |
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author | Cree, Bruce A. C. Hollenbach, Jill A. Bove, Riley Kirkish, Gina Sacco, Simone Caverzasi, Eduardo Bischof, Antje Gundel, Tristan Zhu, Alyssa H. Papinutto, Nico Stern, William A. Bevan, Carolyn Romeo, Andrew Goodin, Douglas S. Gelfand, Jeffrey M. Graves, Jennifer Green, Ari J. Wilson, Michael R. Zamvil, Scott S. Zhao, Chao Gomez, Refujia Ragan, Nicholas R. Rush, Gillian Q. Barba, Patrick Santaniello, Adam Baranzini, Sergio E. Oksenberg, Jorge R. Henry, Roland G. Hauser, Stephen L. |
author_facet | Cree, Bruce A. C. Hollenbach, Jill A. Bove, Riley Kirkish, Gina Sacco, Simone Caverzasi, Eduardo Bischof, Antje Gundel, Tristan Zhu, Alyssa H. Papinutto, Nico Stern, William A. Bevan, Carolyn Romeo, Andrew Goodin, Douglas S. Gelfand, Jeffrey M. Graves, Jennifer Green, Ari J. Wilson, Michael R. Zamvil, Scott S. Zhao, Chao Gomez, Refujia Ragan, Nicholas R. Rush, Gillian Q. Barba, Patrick Santaniello, Adam Baranzini, Sergio E. Oksenberg, Jorge R. Henry, Roland G. Hauser, Stephen L. |
collection | PubMed |
description | OBJECTIVE: Rates of worsening and evolution to secondary progressive multiple sclerosis (MS) may be substantially lower in actively treated patients compared to natural history studies from the pretreatment era. Nonetheless, in our recently reported prospective cohort, more than half of patients with relapsing MS accumulated significant new disability by the 10th year of follow‐up. Notably, “no evidence of disease activity” at 2 years did not predict long‐term stability. Here, we determined to what extent clinical relapses and radiographic evidence of disease activity contribute to long‐term disability accumulation. METHODS: Disability progression was defined as an increase in Expanded Disability Status Scale (EDSS) of 1.5, 1.0, or 0.5 (or greater) from baseline EDSS = 0, 1.0–5.0, and 5.5 or higher, respectively, assessed from baseline to year 5 (±1 year) and sustained to year 10 (±1 year). Longitudinal analysis of relative brain volume loss used a linear mixed model with sex, age, disease duration, and HLA‐DRB1*15:01 as covariates. RESULTS: Relapses were associated with a transient increase in disability over 1‐year intervals (p = 0.012) but not with confirmed disability progression (p = 0.551). Relative brain volume declined at a greater rate among individuals with disability progression compared to those who remained stable (p < 0.05). INTERPRETATION: Long‐term worsening is common in relapsing MS patients, is largely independent of relapse activity, and is associated with accelerated brain atrophy. We propose the term silent progression to describe the insidious disability that accrues in many patients who satisfy traditional criteria for relapsing–remitting MS. Ann Neurol 2019;85:653–666 |
format | Online Article Text |
id | pubmed-6518998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65189982019-05-21 Silent progression in disease activity–free relapsing multiple sclerosis Cree, Bruce A. C. Hollenbach, Jill A. Bove, Riley Kirkish, Gina Sacco, Simone Caverzasi, Eduardo Bischof, Antje Gundel, Tristan Zhu, Alyssa H. Papinutto, Nico Stern, William A. Bevan, Carolyn Romeo, Andrew Goodin, Douglas S. Gelfand, Jeffrey M. Graves, Jennifer Green, Ari J. Wilson, Michael R. Zamvil, Scott S. Zhao, Chao Gomez, Refujia Ragan, Nicholas R. Rush, Gillian Q. Barba, Patrick Santaniello, Adam Baranzini, Sergio E. Oksenberg, Jorge R. Henry, Roland G. Hauser, Stephen L. Ann Neurol Research Articles OBJECTIVE: Rates of worsening and evolution to secondary progressive multiple sclerosis (MS) may be substantially lower in actively treated patients compared to natural history studies from the pretreatment era. Nonetheless, in our recently reported prospective cohort, more than half of patients with relapsing MS accumulated significant new disability by the 10th year of follow‐up. Notably, “no evidence of disease activity” at 2 years did not predict long‐term stability. Here, we determined to what extent clinical relapses and radiographic evidence of disease activity contribute to long‐term disability accumulation. METHODS: Disability progression was defined as an increase in Expanded Disability Status Scale (EDSS) of 1.5, 1.0, or 0.5 (or greater) from baseline EDSS = 0, 1.0–5.0, and 5.5 or higher, respectively, assessed from baseline to year 5 (±1 year) and sustained to year 10 (±1 year). Longitudinal analysis of relative brain volume loss used a linear mixed model with sex, age, disease duration, and HLA‐DRB1*15:01 as covariates. RESULTS: Relapses were associated with a transient increase in disability over 1‐year intervals (p = 0.012) but not with confirmed disability progression (p = 0.551). Relative brain volume declined at a greater rate among individuals with disability progression compared to those who remained stable (p < 0.05). INTERPRETATION: Long‐term worsening is common in relapsing MS patients, is largely independent of relapse activity, and is associated with accelerated brain atrophy. We propose the term silent progression to describe the insidious disability that accrues in many patients who satisfy traditional criteria for relapsing–remitting MS. Ann Neurol 2019;85:653–666 John Wiley & Sons, Inc. 2019-03-30 2019-05 /pmc/articles/PMC6518998/ /pubmed/30851128 http://dx.doi.org/10.1002/ana.25463 Text en © 2019 The Authors. Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Cree, Bruce A. C. Hollenbach, Jill A. Bove, Riley Kirkish, Gina Sacco, Simone Caverzasi, Eduardo Bischof, Antje Gundel, Tristan Zhu, Alyssa H. Papinutto, Nico Stern, William A. Bevan, Carolyn Romeo, Andrew Goodin, Douglas S. Gelfand, Jeffrey M. Graves, Jennifer Green, Ari J. Wilson, Michael R. Zamvil, Scott S. Zhao, Chao Gomez, Refujia Ragan, Nicholas R. Rush, Gillian Q. Barba, Patrick Santaniello, Adam Baranzini, Sergio E. Oksenberg, Jorge R. Henry, Roland G. Hauser, Stephen L. Silent progression in disease activity–free relapsing multiple sclerosis |
title | Silent progression in disease activity–free relapsing multiple sclerosis |
title_full | Silent progression in disease activity–free relapsing multiple sclerosis |
title_fullStr | Silent progression in disease activity–free relapsing multiple sclerosis |
title_full_unstemmed | Silent progression in disease activity–free relapsing multiple sclerosis |
title_short | Silent progression in disease activity–free relapsing multiple sclerosis |
title_sort | silent progression in disease activity–free relapsing multiple sclerosis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518998/ https://www.ncbi.nlm.nih.gov/pubmed/30851128 http://dx.doi.org/10.1002/ana.25463 |
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