Long COVID in People With Multiple Sclerosis and Related Disorders: A Multicenter Cross‐Sectional Study
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· 2025
· Open Access
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· DOI: https://doi.org/10.1002/acn3.70184
Background Managing long COVID in people with multiple sclerosis and related disorders (pwMSRD) is complex due to overlapping symptoms. To address evidence gaps, we evaluated long COVID susceptibility in pwMSRD versus controls and its associations with multi‐domain function and disability. Methods In this multicenter cross‐sectional study, participants completed a survey covering 71 post‐infection symptoms, distinguishing new‐onset from worsening symptoms. We defined long COVID using the 2024 NASEM criteria. Logistic regression assessed long COVID odds. Linear and Poisson regression evaluated associations with function and disability. Results 969 pwMSRD (82.5% female, mean age 51.8 years, 63.5% infected) and 1003 controls (79.4% female, mean age 45.2 years, 61.2% infected) were included. PwMSRD had higher odds of long COVID (aOR = 1.6 [1.2–2.1]), with a stronger association when restricting to worsening symptoms (aOR = 2.3 [1.7–3.1]). Having long COVID was associated with worse physical function, cognition, and depression in both groups. PwMSRD with long COVID experienced greater physical function declines and more depression severity exacerbation than controls, and had faster disability progression compared to those without long COVID. Conclusion PwMSRD show increased susceptibility to long COVID, primarily driven by worsening symptoms. Long COVID contributes to more functional decline and disability worsening. Recognizing and managing long COVID is essential for pwMSRD.
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- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1002/acn3.70184
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.70184
- OA Status
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- References
- 38
- Related Works
- 10
- OpenAlex ID
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Raw OpenAlex JSON
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https://openalex.org/W4414018812Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1002/acn3.70184Digital Object Identifier
- Title
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Long
COVID in People With Multiple Sclerosis and Related Disorders: A Multicenter Cross‐Sectional StudyWork title - Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2025Year of publication
- Publication date
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2025-09-05Full publication date if available
- Authors
-
Chen Hu, Jiyeon Son, Lindsay McAlpine, Elizabeth Walker, Megan Dahl, Emily Song, Sugeidy Ferreira Brito, Katelyn Kavak, Kaho Onomichi, Amit Bar‐Or, Christopher Perrone, Claire Riley, Bianca Weinstock‐Guttman, Philip L. De Jager, Erin E. Longbrake, Zongqi XiaList of authors in order
- Landing page
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https://doi.org/10.1002/acn3.70184Publisher landing page
- PDF URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.70184Direct link to full text PDF
- Open access
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YesWhether a free full text is available
- OA status
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goldOpen access status per OpenAlex
- OA URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.70184Direct OA link when available
- Concepts
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Medicine, Depression (economics), Odds, Logistic regression, Cross-sectional study, Odds ratio, Coronavirus disease 2019 (COVID-19), Poisson regression, Multiple sclerosis, Exacerbation, Internal medicine, Psychiatry, Disease, Pathology, Population, Infectious disease (medical specialty), Economics, Macroeconomics, Environmental healthTop concepts (fields/topics) attached by OpenAlex
- Cited by
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0Total citation count in OpenAlex
- References (count)
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38Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.Poisson | 77 |
| abstract_inverted_index.Results | 85 |
| abstract_inverted_index.address | 21 |
| abstract_inverted_index.complex | 15 |
| abstract_inverted_index.decline | 194 |
| abstract_inverted_index.defined | 61 |
| abstract_inverted_index.female, | 89, 100 |
| abstract_inverted_index.greater | 153 |
| abstract_inverted_index.groups. | 147 |
| abstract_inverted_index.pwMSRD. | 206 |
| abstract_inverted_index.related | 11 |
| abstract_inverted_index.without | 172 |
| abstract_inverted_index.(pwMSRD) | 13 |
| abstract_inverted_index.ABSTRACT | 0 |
| abstract_inverted_index.Logistic | 69 |
| abstract_inverted_index.Managing | 2 |
| abstract_inverted_index.assessed | 71 |
| abstract_inverted_index.compared | 169 |
| abstract_inverted_index.controls | 32, 98 |
| abstract_inverted_index.covering | 51 |
| abstract_inverted_index.declines | 156 |
| abstract_inverted_index.evidence | 22 |
| abstract_inverted_index.function | 38, 82, 155 |
| abstract_inverted_index.managing | 200 |
| abstract_inverted_index.multiple | 8 |
| abstract_inverted_index.physical | 140, 154 |
| abstract_inverted_index.severity | 160 |
| abstract_inverted_index.stronger | 122 |
| abstract_inverted_index.symptoms | 128 |
| abstract_inverted_index.completed | 48 |
| abstract_inverted_index.controls, | 163 |
| abstract_inverted_index.criteria. | 68 |
| abstract_inverted_index.disorders | 12 |
| abstract_inverted_index.essential | 204 |
| abstract_inverted_index.evaluated | 25, 79 |
| abstract_inverted_index.function, | 141 |
| abstract_inverted_index.included. | 108 |
| abstract_inverted_index.increased | 178 |
| abstract_inverted_index.infected) | 95, 106 |
| abstract_inverted_index.primarily | 183 |
| abstract_inverted_index.sclerosis | 9 |
| abstract_inverted_index.symptoms, | 54 |
| abstract_inverted_index.symptoms. | 19, 59, 187 |
| abstract_inverted_index.worsening | 58, 127, 186 |
| abstract_inverted_index.Background | 1 |
| abstract_inverted_index.Conclusion | 175 |
| abstract_inverted_index.associated | 137 |
| abstract_inverted_index.cognition, | 142 |
| abstract_inverted_index.depression | 144, 159 |
| abstract_inverted_index.disability | 167, 196 |
| abstract_inverted_index.functional | 193 |
| abstract_inverted_index.regression | 70, 78 |
| abstract_inverted_index.worsening. | 197 |
| abstract_inverted_index.Recognizing | 198 |
| abstract_inverted_index.association | 123 |
| abstract_inverted_index.contributes | 190 |
| abstract_inverted_index.disability. | 40, 84 |
| abstract_inverted_index.experienced | 152 |
| abstract_inverted_index.multicenter | 44 |
| abstract_inverted_index.new‐onset | 56 |
| abstract_inverted_index.overlapping | 18 |
| abstract_inverted_index.progression | 168 |
| abstract_inverted_index.restricting | 125 |
| abstract_inverted_index.associations | 35, 80 |
| abstract_inverted_index.exacerbation | 161 |
| abstract_inverted_index.participants | 47 |
| abstract_inverted_index.[1.2–2.1]), | 119 |
| abstract_inverted_index.[1.7–3.1]). | 132 |
| abstract_inverted_index.distinguishing | 55 |
| abstract_inverted_index.multi‐domain | 37 |
| abstract_inverted_index.susceptibility | 28, 179 |
| abstract_inverted_index.post‐infection | 53 |
| abstract_inverted_index.cross‐sectional | 45 |
| cited_by_percentile_year | |
| corresponding_author_ids | https://openalex.org/A5069572535 |
| countries_distinct_count | 1 |
| institutions_distinct_count | 16 |
| corresponding_institution_ids | https://openalex.org/I170201317 |
| citation_normalized_percentile.value | 0.50882909 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |