Abstract
Social determinants of health are the conditions in which people are born, grow, live, work and age. These circumstances are the non-medical factors that influence health outcomes. Evidence indicates that health behaviours, comorbidities and disease-modifying therapies all contribute to multiple sclerosis (MS) outcomes; however, our knowledge of the effects of social determinants — that is, the ‘risks of risks’ — on health has not yet changed our approach to MS. Assessing and addressing social determinants of health could fundamentally improve health and health care in MS; this approach has already been successful in improving outcomes in other chronic diseases. In this narrative Review, we identify and discuss the body of evidence supporting an effect of many social determinants of health, including racial background, employment and social support, on MS outcomes. It must be noted that many of the published studies were subject to bias, and screening tools and/or practical interventions that address these social determinants are, for the most part, lacking. The existing work does not fully explore the potential bidirectional and complex relationships between social determinants of health and MS, and the interpretation of findings is complicated by the interactions and intersections among many of the identified determinants. On the basis of the reviewed literature, we consider that, if effective interventions targeting social determinants of health were available, they could have substantial effects on MS outcomes. Therefore, funding for and focused design of studies to evaluate and address social determinants of health are urgently needed.
Key points
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Addressing an individual’s social determinants of health — that is, the conditions under which they are born, grow, live, work and age — could provide opportunities to reduce the burden of living with multiple sclerosis (MS).
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Individual factors that may influence MS-related outcomes include sex, gender and sexuality, race and ethnicity, education and employment, socioeconomic status, and domestic abuse.
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Societal infrastructures, including access to food, health care and social support, can also affect MS-related outcomes.
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Awareness of the specific circumstances of a patient with MS might help neurologists deliver better care.
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Social determinants of health are not static and can change according to wider sociopolitical contexts, as highlighted by the COVID-19 pandemic.
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Rigorous studies of interventions to ameliorate the effects of poor social determinants on people with MS are urgently needed.
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Acknowledgements
This work received no specific funding. R.D. works within the Preventive Neurology Unit, which is part funded by Barts Charity. Y.L. and C.H.M. are funded by MS Australia fellowships.
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R.D., D.R.R., M.D., R.H., Y.L., F.J.M., S.R., M.J.W., G.G. and H.L.F. researched data for the article. All authors contributed substantially to discussion of the content. R.D., D.R.R., M.D., R.H., Y.L., F.J.M., S.R., M.J.W., G.G. and H.L.F wrote the article. All authors reviewed and/or edited the manuscript before submission.
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Review criteria To ensure an inclusive overview, we searched PubMed, Scopus, CINAHL through EBSCOhost, MEDLINE through OVID, all other Web of Science (BCI OR SciELO OR WoS OR CABI OR RSCI OR CCC) core collection, PsychINFO and Emcare (OVID) using a search strategy based on the WHO social and immediate determinants of health and a wide range of MS terms on 17 January 2022. We considered any original studies examining social determinants of health and MS outcomes from 2004 onwards, and did not restrict based on language, given the wide-reaching effects of social determinants of health. Out of 2,453 papers screened, a total of 194 papers were considered for inclusion, and the final decision was based on relevance to social determinants of health and MS, along with novelty and current relevance.
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Dobson, R., Rice, D.R., D’hooghe, M. et al. Social determinants of health in multiple sclerosis. Nat Rev Neurol 18, 723–734 (2022). https://doi.org/10.1038/s41582-022-00735-5
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DOI: https://doi.org/10.1038/s41582-022-00735-5
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Marriage is associated with decreased lesion volumes and less brain atrophy in people with multiple sclerosis
Journal of Neurology (2025)
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Real-World Treatment Outcomes in Black, Hispanic, Asian, and White People with Multiple Sclerosis Treated with Fumarates in the USA
Neurology and Therapy (2025)
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Multiple Sclerosis in People of Diverse Racial and Ethnic Backgrounds: Presentation, Disease Course, and Interactions with Disease-Modifying Therapy
CNS Drugs (2025)