Multiple sclerosis is an inflammatory disease of the central nervous system, with a posited hypoxia-inflammation cycle hypothesis. Hypoxia may increase disease severity in MS. We found R2* was increased (an MRI marker of hypoxia) in the cortex. We observed increased sickness and R2* in EAE mice compared to controls, but reduced CBF in both CFA-PTx and EAE. Inflammation is in both groups, while autoimmunity is only in EAE. Reduced CBF may relate to inflammation, whereas hypoxia may relate to autoimmune-mediated damage and increase disease severity.
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Muhammed et al. (2024) studied this question.
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