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Cited by 440

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Long‐term evolution of multiple sclerosis disability in the treatment era

Open access
University of California, San Francisco MS‐EPIC Team:, Cree, Bruce A. C., Gourraud, Pierre‐Antoine, Oksenberg, Jorge R., Bevan, Carolyn, Crabtree‐Hartman, Elizabeth, Gelfand, Jeffrey M., Goodin, Douglas S., Graves, Jennifer, Green, Ari J., Mowry, Ellen, Okuda, Darin T., Pelletier, Daniel, von Büdingen, H.‐Christian, Zamvil, Scott S., Agrawal, Alisha, Caillier, Stacy, Ciocca, Caroline, Gomez, Refujia, Kanner, Rachel, Lincoln, Robin, Lizee, Antoine, Qualley, Pamela, Santaniello, Adam, Suleiman, Leena, Bucci, Monica, Panara, Valentina, Papinutto, Nico, Stern, William A., Zhu, Alyssa H., Cutter, Gary R., Baranzini, Sergio, Henry, Roland G., Hauser, Stephen L.·2016·Annals of Neurology

Abstract

Objective: To characterize the accrual of long‐term disability in a cohort of actively treated multiple sclerosis (MS) patients and to assess whether clinical and magnetic resonance imaging (MRI) data used in clinical trials have long‐term prognostic value. Methods: This is a prospective study of 517 actively managed MS patients enrolled at a single center. Results: More than 91% of patients were retained, with data ascertained up to 10 years after the baseline visit. At this last assessment, neurologic disability as measured by the Expanded Disability Status Scale (EDSS) was stable or improved compared to baseline in 41% of patients. Subjects with no evidence of disease activity (NEDA) by clinical and MRI criteria during the first 2 years had long‐term outcomes that were no different from those of the cohort as a whole. 25‐OH vitamin D serum levels were inversely associated with short‐term MS disease activity; however, these levels had no association with long‐term disability. At a median time of 16.8 years after disease onset, 10.7% (95% confidence interval [CI] = 7.2–14%) of patients reached an EDSS ≥ 6, and 18.1% (95% CI = 13.5–22.5%) evolved from relapsing MS to secondary progressive MS (SPMS). Interpretation: Rates of worsening and evolution to SPMS were substantially lower when compared to earlier natural history studies. Notably, the NEDA 2‐year endpoint was not a predictor of long‐term stability. Finally, the data call into question the utility of annual MRI assessments as a treat‐to‐target approach for MS care. Ann Neurol 2016;80:499–510

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Metadata

Authors
University of California, S. F. M. T., Cree, B. A. C., Gourraud, P., Oksenberg, J. R., Bevan, C., Crabtree‐Hartman, E., Gelfand, J. M., Goodin, D. S., Graves, J., Green, A. J., Mowry, E., Okuda, D. T., Pelletier, D., von Büdingen, H. ‐., Zamvil, S. S., Agrawal, A., Caillier, S., Ciocca, C., Gomez, R., Kanner, R., Lincoln, R., Lizee, A., Qualley, P., Santaniello, A., Suleiman, L., Bucci, M., Panara, V., Papinutto, N., Stern, W. A., Zhu, A. H., Cutter, G. R., Baranzini, S., Henry, R. G., & Hauser, S. L.
Venue
Annals of Neurology
Publisher
Wiley
Published
2016-08-13
Volume
80
Issue
4
Pages
499-510
ISSN
  • 0364-5134 (ISSN-L)
  • 1531-8249
OpenAlex
W2489432788
Cited by
440
References
5
FWCI
35.70
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Long‐term evolution of multiple sclerosis disability in the treatment era. https://app.cochat.ai/papers/10.1002/ana.24747
The paper
University of California, S. F. M. T., Cree, B. A. C., Gourraud, P., Oksenberg, J. R., Bevan, C., Crabtree‐Hartman, E., Gelfand, J. M., Goodin, D. S., Graves, J., Green, A. J., Mowry, E., Okuda, D. T., Pelletier, D., von Büdingen, H. ‐., Zamvil, S. S., Agrawal, A., Caillier, S., Ciocca, C., Gomez, R., . . . Hauser, S. L. (2016). Long‐term evolution of multiple sclerosis disability in the treatment era. Annals of Neurology. https://doi.org/10.1002/ana.24747

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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