Nabeela Nathoo , Nur Neyal , Jiye Son , Christopher G. Schwarz , Elizabeth J. Atkinson , Holly A. Morrison , June Kendall Thomas , John D. Port , Kejal Kantarci , Orhun H. Kantarci , Burcu Zeydan
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引用次数: 0
Abstract
Background
African American persons with MS (AApwMS) have more aggressive clinical and imaging outcomes than White American pwMS (WApwMS), including lower brain and spinal cord (SC) volumes. However, imaging studies are lacking considering the effects of sex, race, and ethnicity together.
Objective
Compare MS clinical and imaging features among AApwMS and WApwMS, incorporating the modifying effects of sex, race, and ethnicity.
Methods
Clinical variables and MRI were obtained for AApwMS and WApwMS.
Results
Thirty-five MRIs in 28 AApwMS (61 % female) and 255 MRIs in 91 WApwMS (68 % female) were evaluated. AApwMS had a shorter MS disease duration (median 5.9 years, IQR 2.7–13.1) compared to WApwMS (9.4 years, IQR 3.8–17.0; p = 0.034). Fewer AApwMS ever used disease modifying therapy (69 %) compared to WApwMS (92 %; p < 0.001), while the likelihood of having progressive MS and developing severe disability were similar between groups (p > 0.05). AA women with MS had smaller thalamus (p = 0.016), cerebellar grey matter (p = 0.025), and SC-C2 (p = 0.005) volumes than WA women with MS. Although multiple brain and SC regions were smaller in AA men than WA men with MS, the differences were not significant.
Conclusion
Interaction between sex, race, and ethnicity may influence differences in imaging metrics of key central nervous system relays, likely preceding clinical worsening in MS.
期刊介绍:
The Journal of Neuroimmunology affords a forum for the publication of works applying immunologic methodology to the furtherance of the neurological sciences. Studies on all branches of the neurosciences, particularly fundamental and applied neurobiology, neurology, neuropathology, neurochemistry, neurovirology, neuroendocrinology, neuromuscular research, neuropharmacology and psychology, which involve either immunologic methodology (e.g. immunocytochemistry) or fundamental immunology (e.g. antibody and lymphocyte assays), are considered for publication.