Characteristics of multiple sclerosis and demyelinating disease in an Asian American population.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
09 2023
Historique:
medline: 15 9 2023
pubmed: 7 8 2023
entrez: 7 8 2023
Statut: ppublish

Résumé

Race and ancestry influence the course of multiple sclerosis (MS). Explore clinical characteristics of MS and neuromyelitis optica spectrum disorder (NMOSD) in Asian American patients. Chart review was performed for 282 adults with demyelinating disease who self-identified as Asian at a single North American MS center. Demographics and clinical characteristics were compared to non-Asian MS patients and by region of Asian ancestry. Region of ancestry was known for 181 patients. Most (94.7%) preferred English, but fewer East Asian patients did (80%, MS severity was similar between Asian American patients and non-Asian patients. Region of ancestry was associated with differences in sociodemographics and MS severity. Further research is needed to uncover genetic, socioeconomic, or environmental factors causing these differences.

Sections du résumé

BACKGROUND
Race and ancestry influence the course of multiple sclerosis (MS).
OBJECTIVES
Explore clinical characteristics of MS and neuromyelitis optica spectrum disorder (NMOSD) in Asian American patients.
METHODS
Chart review was performed for 282 adults with demyelinating disease who self-identified as Asian at a single North American MS center. Demographics and clinical characteristics were compared to non-Asian MS patients and by region of Asian ancestry.
RESULTS
Region of ancestry was known for 181 patients. Most (94.7%) preferred English, but fewer East Asian patients did (80%,
CONCLUSIONS
MS severity was similar between Asian American patients and non-Asian patients. Region of ancestry was associated with differences in sociodemographics and MS severity. Further research is needed to uncover genetic, socioeconomic, or environmental factors causing these differences.

Identifiants

pubmed: 37548214
doi: 10.1177/13524585231188486
doi:

Substances chimiques

Aquaporin 4 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1216-1228

Auteurs

Jessica H Fan (JH)

Department of Neurology, UCSF Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA.
Department of Neurology, Kaiser Permanente, Oakland, CA, USA.

Jessa Alexander (J)

Department of Neurology, UCSF Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA.

Shane Poole (S)

Department of Neurology, UCSF Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA.

Jaeleene Wijangco (J)

Department of Neurology, UCSF Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA.

Lily J Henson (LJ)

Piedmont Henry Hospital, Stockbridge, GA, USA.

Ruth Dobson (R)

Preventive Neurology Unit, Wolfson Institute of Population Health, Queen Mary University, London, UK.
Department of Neurology, Royal London Hospital, London, UK.

Chu-Yueh Guo (CY)

Department of Neurology, UCSF Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA.

Riley Bove (R)

Department of Neurology, UCSF Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA.

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Classifications MeSH