Predictors of Long-Term Visual Acuity in a Modern Cohort of Patients With Acute Idiopathic and Multiple Sclerosis-Associated Optic Neuritis.
Journal
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
ISSN: 1536-5166
Titre abrégé: J Neuroophthalmol
Pays: United States
ID NLM: 9431308
Informations de publication
Date de publication:
01 Dec 2023
01 Dec 2023
Historique:
pmc-release:
18
11
2024
medline:
27
11
2023
pubmed:
18
5
2023
entrez:
18
5
2023
Statut:
ppublish
Résumé
For patients with idiopathic or multiple sclerosis (MS)-associated optic neuritis (ON), the largest multicenter clinical trial (Optic Neuritis Treatment Trial [ONTT]) showed excellent visual outcomes and baseline high-contrast visual acuity (HCVA) was the only predictor of HCVA at 1 year. We aimed to evaluate predictors of long-term HCVA in a modern, real-world population of patients with ON and compare with previously published ONTT models. We performed a retrospective, longitudinal, observational study at the University of Michigan and the University of Calgary evaluating 135 episodes of idiopathic or MS-associated ON in 118 patients diagnosed by a neuro-ophthalmologist within 30 days of onset (January 2011-June 2021). Primary outcome measured was HCVA (Snellen equivalents) at 6-18 months. Multiple linear regression models of 107 episodes from 93 patients assessed the association between HCVA at 6-18 months and age, sex, race, pain, optic disc swelling, symptoms (days), viral illness prodrome, MS status, high-dose glucocorticoid treatment, and baseline HCVA. Of the 135 acute episodes (109 Michigan and 26 Calgary), median age at presentation was 39 years (interquartile range [IQR], 31-49 years), 91 (67.4%) were women, 112 (83.0%) were non-Hispanic Caucasians, 101 (75.9%) had pain, 33 (24.4%) had disc edema, 8 (5.9%) had a viral prodrome, 66 (48.9%) had MS, and 62 (46.6%) were treated with glucocorticoids. The median (IQR) time between symptom onset and diagnosis was 6 days (range, 4-11 days). The median (IQR) HCVA at baseline and at 6-18 months were 20/50 (20/22, 20/200) and 20/20 (20/20, 20/27), respectively; 62 (45.9%) had better than 20/40 at baseline and 117 (86.7%) had better than 20/40 at 6-18 months. In linear regression models (n = 107 episodes in 93 patients with baseline HCVA better than CF), only baseline HCVA (β = 0.076; P = 0.027) was associated with long-term HCVA. Regression coefficients were similar and within the 95% confidence interval of coefficients from published ONTT models. In a modern cohort of patients with idiopathic or MS-associated ON with baseline HCVA better than CF, long-term outcomes were good, and the only predictor was baseline HCVA. These findings were similar to prior analyses of ONTT data, and as a result, these are validated for use in conveying prognostic information about long-term HCVA outcomes.
Sections du résumé
BACKGROUND
BACKGROUND
For patients with idiopathic or multiple sclerosis (MS)-associated optic neuritis (ON), the largest multicenter clinical trial (Optic Neuritis Treatment Trial [ONTT]) showed excellent visual outcomes and baseline high-contrast visual acuity (HCVA) was the only predictor of HCVA at 1 year. We aimed to evaluate predictors of long-term HCVA in a modern, real-world population of patients with ON and compare with previously published ONTT models.
METHODS
METHODS
We performed a retrospective, longitudinal, observational study at the University of Michigan and the University of Calgary evaluating 135 episodes of idiopathic or MS-associated ON in 118 patients diagnosed by a neuro-ophthalmologist within 30 days of onset (January 2011-June 2021). Primary outcome measured was HCVA (Snellen equivalents) at 6-18 months. Multiple linear regression models of 107 episodes from 93 patients assessed the association between HCVA at 6-18 months and age, sex, race, pain, optic disc swelling, symptoms (days), viral illness prodrome, MS status, high-dose glucocorticoid treatment, and baseline HCVA.
RESULTS
RESULTS
Of the 135 acute episodes (109 Michigan and 26 Calgary), median age at presentation was 39 years (interquartile range [IQR], 31-49 years), 91 (67.4%) were women, 112 (83.0%) were non-Hispanic Caucasians, 101 (75.9%) had pain, 33 (24.4%) had disc edema, 8 (5.9%) had a viral prodrome, 66 (48.9%) had MS, and 62 (46.6%) were treated with glucocorticoids. The median (IQR) time between symptom onset and diagnosis was 6 days (range, 4-11 days). The median (IQR) HCVA at baseline and at 6-18 months were 20/50 (20/22, 20/200) and 20/20 (20/20, 20/27), respectively; 62 (45.9%) had better than 20/40 at baseline and 117 (86.7%) had better than 20/40 at 6-18 months. In linear regression models (n = 107 episodes in 93 patients with baseline HCVA better than CF), only baseline HCVA (β = 0.076; P = 0.027) was associated with long-term HCVA. Regression coefficients were similar and within the 95% confidence interval of coefficients from published ONTT models.
CONCLUSIONS
CONCLUSIONS
In a modern cohort of patients with idiopathic or MS-associated ON with baseline HCVA better than CF, long-term outcomes were good, and the only predictor was baseline HCVA. These findings were similar to prior analyses of ONTT data, and as a result, these are validated for use in conveying prognostic information about long-term HCVA outcomes.
Identifiants
pubmed: 37200095
doi: 10.1097/WNO.0000000000001870
pii: 00041327-990000000-00355
pmc: PMC10656360
mid: NIHMS1885239
doi:
Substances chimiques
Glucocorticoids
0
Types de publication
Observational Study
Multicenter Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
475-480Subventions
Organisme : NEI NIH HHS
ID : K23 EY027849
Pays : United States
Informations de copyright
Copyright © 2023 by North American Neuro-Ophthalmology Society.
Déclaration de conflit d'intérêts
A. Jarocki, L. A. Gonzalez, C. A. Andrews, and K. A. Kerber: no conflicts of interest to disclose; E. Benard-Seguin : Neuro Nexus Hackathon Grant and Fighting Blindness Canada received from University of Calgary; F. Costello: consulting fees received from Accure Therapeutics and Frequency Therapeutics. Payment for lectures received from Novartis and Alexion; L. B. De Lott: funding received from K23EY027849 grant and North American Neuro-Ophthalmology Society Pilot Grant. Payment for lectures received from the American Academy of Neurology.
Références
Neurology. 2010 Jul 20;75(3):217-23
pubmed: 20644149
Neurology. 2014 Jun 17;82(24):2173-9
pubmed: 24850491
Neurology. 2010 Mar 30;74(13):1041-7
pubmed: 20350978
JAMA Netw Open. 2020 May 1;3(5):e204339
pubmed: 32379333
JAMA Neurol. 2018 Jun 1;75(6):690-696
pubmed: 29507942
Ann Neurol. 2015 Feb;77(2):228-36
pubmed: 25382184
Am J Ophthalmol. 2020 Dec;220:110-114
pubmed: 32707199
JAMA Ophthalmol. 2014 Apr 1;132(4):421-7
pubmed: 24557028
Mult Scler. 2008 Sep;14(8):1031-5
pubmed: 18632778
J Neurol. 2022 Mar;269(3):1663-1669
pubmed: 34392376
N Engl J Med. 1992 Feb 27;326(9):581-8
pubmed: 1734247
Lancet Neurol. 2018 Feb;17(2):162-173
pubmed: 29275977
Neurology. 2015 Jul 14;85(2):177-89
pubmed: 26092914
Ophthalmology. 2007 Apr;114(4):810-5
pubmed: 17141316
Ann Neurol. 2011 Feb;69(2):292-302
pubmed: 21387374
J Neurol. 2022 Jan;269(1):111-124
pubmed: 33389032
J Neurol Sci. 2014 Dec 15;347(1-2):23-33
pubmed: 25454639
Arch Neurol. 1998 Feb;55(2):186-92
pubmed: 9482360
Mult Scler. 2019 Nov;25(13):1754-1763
pubmed: 30303037
J Neurol Sci. 2009 Jan 15;276(1-2):69-74
pubmed: 18926549