TY - JOUR
T1 - Long-term outcomes in patients presenting with optic neuritis
T2 - Analyses of the MSBase registry
AU - the MSBase Study Group
AU - Kenney, Rachel
AU - Liu, Mengling
AU - Patil, Sachi
AU - Alroughani, Raed
AU - Ampapa, Radek
AU - Bergamaschi, Roberto
AU - Boz, Cavit
AU - Butzkueven, Helmut
AU - Gomez, Jose Cabrera
AU - Cartechini, Elisabetta
AU - Madueño, Sara Eichau
AU - Ferraro, Diana
AU - Grand-Maison, Francois
AU - Granella, Franco
AU - Horakova, Dana
AU - Izquierdo Ayuso, Guillermo
AU - Kalincik, Tomas
AU - Lizrova Preiningerova, Jana
AU - Lugaresi, Alessandra
AU - Onofrj, Marco
AU - Ozakbas, Serkan
AU - Patti, Francesco
AU - Sola, Patrizia
AU - Soysal, Aysun
AU - Spitaleri, Daniele Litterio A.
AU - Terzi, Murat
AU - Turkoglu, Recai
AU - van Pesch, Vincent
AU - Saidha, Shiv
AU - Thorpe, Lorna E.
AU - Galetta, Steven L.
AU - Balcer, Laura J.
AU - Kister, Ilya
AU - Spelman, Tim
N1 - Funding Information:
Alessandra Lugaresi has served as a Biogen, Merck Serono, Novartis, Roche, Sanofi/ Genzyme and Teva Advisory Board Member. She received congress and travel/accommodation expense compensations or speaker honoraria from Biogen, Merck, Mylan, Novartis, Sanofi/Genzyme, Teva and Fondazione Italiana Sclerosi Multipla (FISM). Her institutions received research grants from Novartis.
Funding Information:
Shiv Saidha has received consulting fees from Medical Logix for the development of CME programs in neurology and has served on scientific advisory boards for Biogen, Genzyme, Genentech Corporation, EMD Serono & Celgene. He has consulted for Carl Zeiss Meditec. He is the PI of investigator-initiated studies funded by Genentech Corporation and Biogen Idec , and received support from the Race to Erase MS foundation . He has received equity compensation for consulting from JuneBrain LLC, a retinal imaging device developer.
Funding Information:
Tomas Kalincik served on scientific advisory boards for BMS, Roche, Sanofi Genzyme, Novartis, Merck and Biogen, steering committee for Brain Atrophy Initiative by Sanofi Genzyme, received conference travel support and/or speaker honoraria from WebMD Global, Novartis, Biogen, Sanofi-Genzyme, Teva, BioCSL and Merck and received research or educational event support from Biogen, Novartis, Genzyme, Roche, Celgene and Merck.Shiv Saidha has received consulting fees from Medical Logix for the development of CME programs in neurology and has served on scientific advisory boards for Biogen, Genzyme, Genentech Corporation, EMD Serono & Celgene. He has consulted for Carl Zeiss Meditec. He is the PI of investigator-initiated studies funded by Genentech Corporation and Biogen Idec, and received support from the Race to Erase MS foundation. He has received equity compensation for consulting from JuneBrain LLC, a retinal imaging device developer.This study was supported in part by the NYU School of Medicine.
Publisher Copyright:
© 2021
PY - 2021/11/15
Y1 - 2021/11/15
N2 - Background: Short-term outcomes of optic neuritis (ON) have been well characterized. Limited data exists on longer-term visual outcomes in patients who present with ON. The large MSBase registry allows for characterization of long-term visual outcomes after ON. Methods: Via the MSBase Registry, data on patients from 41 centers was collected during routine clinical and research visits. Physical and visual disability were measured using the expanded disability status scale (EDSS) and the visual function score (VFS). Inclusion criteria for this analysis included age ≥ 18 years, clinically isolated syndrome (CIS), ON-onset, baseline visit within 6 months of onset, and at least one follow-up visit. Survival analysis was used to evaluate the association of disease-modifying treatment with time to conversion to clinically definite MS or sustained EDSS/VFS progression. Results: Data from 60,933 patients were obtained from the MSBase registry in July 2019. Of these, 1317 patients met inclusion criteria; 935 were treated at some point in disease course, while 382 were never treated. At baseline, mean age was 32.3 ± 8.8 years, 74% were female, median EDSS was 2 (IQR 1–2), and median VFS was 1 (IQR 0–2). Median follow-up time was 5.2 years (IQR 2.4–9.3). Treatment was associated with reduced risk and delayed conversion to clinically definite MS (HR = 0.70, p < 0.001), sustained EDSS progression (HR = 0.46, p < 0.0001) and sustained VFS (HR = 0.41, p < 0.001) progression. Conclusions: In the MSBase cohort, treatment after ON was associated with better visual and neurological outcomes compared to no treatment. These results support early treatment for patients presenting with ON as the first manifestation of MS.
AB - Background: Short-term outcomes of optic neuritis (ON) have been well characterized. Limited data exists on longer-term visual outcomes in patients who present with ON. The large MSBase registry allows for characterization of long-term visual outcomes after ON. Methods: Via the MSBase Registry, data on patients from 41 centers was collected during routine clinical and research visits. Physical and visual disability were measured using the expanded disability status scale (EDSS) and the visual function score (VFS). Inclusion criteria for this analysis included age ≥ 18 years, clinically isolated syndrome (CIS), ON-onset, baseline visit within 6 months of onset, and at least one follow-up visit. Survival analysis was used to evaluate the association of disease-modifying treatment with time to conversion to clinically definite MS or sustained EDSS/VFS progression. Results: Data from 60,933 patients were obtained from the MSBase registry in July 2019. Of these, 1317 patients met inclusion criteria; 935 were treated at some point in disease course, while 382 were never treated. At baseline, mean age was 32.3 ± 8.8 years, 74% were female, median EDSS was 2 (IQR 1–2), and median VFS was 1 (IQR 0–2). Median follow-up time was 5.2 years (IQR 2.4–9.3). Treatment was associated with reduced risk and delayed conversion to clinically definite MS (HR = 0.70, p < 0.001), sustained EDSS progression (HR = 0.46, p < 0.0001) and sustained VFS (HR = 0.41, p < 0.001) progression. Conclusions: In the MSBase cohort, treatment after ON was associated with better visual and neurological outcomes compared to no treatment. These results support early treatment for patients presenting with ON as the first manifestation of MS.
KW - Clinically isolated syndrome
KW - Expanded disability status scale (EDSS)
KW - MSBase registry
KW - Optic neuritis
KW - Vision
KW - Disability Evaluation
KW - Humans
KW - Disease Progression
KW - Young Adult
KW - Multiple Sclerosis/complications
KW - Adolescent
KW - Adult
KW - Female
KW - Registries
KW - Demyelinating Diseases
KW - Optic Neuritis/diagnosis
KW - Cohort Studies
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U2 - 10.1016/j.jns.2021.118067
DO - 10.1016/j.jns.2021.118067
M3 - Article
C2 - 34537678
AN - SCOPUS:85115035602
SN - 0022-510X
VL - 430
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
M1 - 118067
ER -