Environmental and genetic risk factors for MS: an integrated review

Emmanuelle Waubant*, Robyn Lucas, Ellen Mowry, Jennifer Graves, Tomas Olsson, Lars Alfredsson, Annette Langer-Gould

*Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    203 Citations (Scopus)

    Abstract

    Recent findings have provided a molecular basis for the combined contributions of multifaceted risk factors for the onset of multiple sclerosis (MS). MS appears to start as a chronic dysregulation of immune homeostasis resulting from complex interactions between genetic predispositions, infectious exposures, and factors that lead to pro-inflammatory states, including smoking, obesity, and low sun exposure. This is supported by the discovery of gene–environment (GxE) interactions and epigenetic alterations triggered by environmental exposures in individuals with particular genetic make-ups. It is notable that several of these pro-inflammatory factors have not emerged as strong prognostic indicators. Biological processes at play during the relapsing phase of the disease may result from initial inflammatory-mediated injury, while risk factors for the later phase of MS, which is weighted toward neurodegeneration, are not yet well defined. This integrated review of current evidence guides recommendations for clinical practice and highlights research gaps.

    Original languageEnglish
    Pages (from-to)1905-1922
    Number of pages18
    JournalAnnals of Clinical and Translational Neurology
    Volume6
    Issue number9
    DOIs
    Publication statusPublished - 1 Sept 2019

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