A national case-control study investigating demographic and environmental factors associated with NMOSD.


Journal

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

Informations de publication

Date de publication:
04 2023
Historique:
medline: 1 5 2023
pubmed: 22 2 2023
entrez: 21 2 2023
Statut: ppublish

Résumé

Risk factors for aquaporin-4 (AQP4+) antibody neuromyelitis optica spectrum disorder (NMOSD) are not well-established. To investigate demographic and environmental factors associated with NMOSD using a validated questionnaire and case-control design. We enrolled patients with AQP4 + NMOSD through six Canadian Multiple Sclerosis Clinics. Participants completed the validated Environmental Risk Factors in Multiple Sclerosis Study (EnvIMS) questionnaire. Their responses were compared to those of 956 unaffected controls from the Canadian arm of EnvIMS. We calculated odds ratios (ORs) for the association between each variable and NMOSD using logistic regression and Firth's procedure for rare events. In 122 participants (87.7% female) with NMOSD, odds of NMOSD in East Asian and Black participants were ⩾8 times that observed in White participants. Birthplace outside Canada was associated with an increased risk of NMOSD (OR = 5.5, 95% confidence interval (CI) = 3.6-8.3) as were concomitant autoimmune diseases (OR = 2.7, 95% CI = 1.4-5.0). No association was observed with reproductive history or age at menarche. In this case-control study, risk of NMOSD in East Asian and Black versus White individuals was greater than that observed in many previous studies. Despite the preponderance of affected women, we did not observe any association with hormonal factors such as reproductive history or age at menarche.

Sections du résumé

BACKGROUND
Risk factors for aquaporin-4 (AQP4+) antibody neuromyelitis optica spectrum disorder (NMOSD) are not well-established.
OBJECTIVE
To investigate demographic and environmental factors associated with NMOSD using a validated questionnaire and case-control design.
METHODS
We enrolled patients with AQP4 + NMOSD through six Canadian Multiple Sclerosis Clinics. Participants completed the validated Environmental Risk Factors in Multiple Sclerosis Study (EnvIMS) questionnaire. Their responses were compared to those of 956 unaffected controls from the Canadian arm of EnvIMS. We calculated odds ratios (ORs) for the association between each variable and NMOSD using logistic regression and Firth's procedure for rare events.
RESULTS
In 122 participants (87.7% female) with NMOSD, odds of NMOSD in East Asian and Black participants were ⩾8 times that observed in White participants. Birthplace outside Canada was associated with an increased risk of NMOSD (OR = 5.5, 95% confidence interval (CI) = 3.6-8.3) as were concomitant autoimmune diseases (OR = 2.7, 95% CI = 1.4-5.0). No association was observed with reproductive history or age at menarche.
CONCLUSION
In this case-control study, risk of NMOSD in East Asian and Black versus White individuals was greater than that observed in many previous studies. Despite the preponderance of affected women, we did not observe any association with hormonal factors such as reproductive history or age at menarche.

Identifiants

pubmed: 36803237
doi: 10.1177/13524585231151953
pmc: PMC10152218
doi:

Substances chimiques

Aquaporin 4 0
Autoantibodies 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

521-529

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Auteurs

Dalia L Rotstein (DL)

Department of Medicine, University of Toronto, Toronto, ON, Canada/MS Clinic, St. Michael's Hospital, Toronto, ON, Canada.

Christina Wolfson (C)

Departments of Epidemiology, Biostatistics and Occupational Health and Medicine, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, Canada/Research Institute of the McGill University Health Centre, Montreal, QC, Canada.

Robert Carruthers (R)

Division of Neurology, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.

Mark S Freedman (MS)

Department of Medicine, University of Ottawa, Ottawa, ON, Canada/Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Sarah A Morrow (SA)

Western University, London, ON, Canada/London Health Sciences Centre, London, ON, Canada.

Liesly Lee (L)

Department of Medicine, University of Toronto, Toronto, ON, Canada/Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canada.

Jodie M Burton (JM)

Departments of Clinical Neurosciences and Community Health Sciences, University of Calgary, Calgary, AB, Canada.

Rosane Nisenbaum (R)

St. Michael's Hospital, Toronto, ON, Canada/Applied Health Research Centre and MAP Centre for Urban Health Solutions, Li Ka Shing Knowledge Institute, St Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada/Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.

Andrea Konig (A)

St. Michael's Hospital, Toronto, ON, Canada.

Sandra Magalhaes (S)

Department of Sociology, University of New Brunswick, Fredericton, NB, Canada.

Ruth Ann Marrie (RA)

Departments of Medicine and Community Health Sciences, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.

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