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. 2024 Nov;30(13):1674-1682.
doi: 10.1177/13524585241286671. Epub 2024 Oct 11.

Employment, work hours, and wages in adults with myelin oligodendrocyte glycoprotein antibody disease: An international cohort study

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Employment, work hours, and wages in adults with myelin oligodendrocyte glycoprotein antibody disease: An international cohort study

Andrew Siyoon Ham et al. Mult Scler. 2024 Nov.

Abstract

Objectives: The objectives were to understand the employment impacts of myelin oligodendrocyte glycoprotein-associated antibody disease (MOGAD) on adults in an international cohort by determining lost employment, work hours, and wages.

Background: Clinically, MOGAD can be associated with significant disability; however, its socioeconomic consequences for adults are barely reported.

Methods: Participants of potential working age (18-70 years old) with neurologist-diagnosed MOGAD were recruited from clinical sites in 13 countries, April 2022 to August 2023. Each participant completed a one-time survey. Regression models assessed associations with post-MOGAD (1) unemployment and (2) work hours.

Results: A total of 117 participants (66.7% female), mean age 39.7 years, median disease duration 3 years (25th, 75th percentile: 1, 7) were analyzed. Employment post-MOGAD reduced from 74 (63.2%) to 57 (48.7%) participants. Participants employed pre-diagnosis reduced their work hours, on average, from 31.6 hours/week to 19.5 hours/week post-diagnosis. Residence in a high-income country was statistically significantly associated with post-diagnosis employment and higher weekly work hours. Depressed mood was associated with unemployment. MOGAD-related pain and history of myelitis were independently associated with lost work hours.

Conclusion: MOGAD can have significant impacts on adult employment, particularly in non-high-income countries. Depressed mood and pain are potentially modifiable factors related to socioeconomic status in MOGAD.

Keywords: Employment; income; myelin oligodendrocyte glycoprotein antibody–associated disease; neurology; outcomes; socioeconomic status.

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Conflict of interest statement

Declaration of Conflicting InterestsThe author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Dr F.J.M. has received research funding to her institution from Alexion, Amgen, EMD Serono, Genentech, Novartis, and TG Therapeutics and consulting fees from Alexion, EMD Serono, Genentech, and Roche. Dr T.Y. has received honoraria from ASNA, Edanz Pharma, Euroimmun AG, Merck, Novartis, Roche, Terumo BCT for consulting services and speaker’s fees, and research grants from the National Medical Research Council (NMRC Singapore), and Roche. Dr A.S. has received research grants from The Turkish Multiple Sclerosis Society; and research grants from The Scientific and Technological Research Council of Turkey & Istanbul University-Cerrahpasa Research Support Funds.

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