» Articles » PMID: 30185189

A Comparison of Brain Magnetic Resonance Imaging Lesions in Multiple Sclerosis by Race with Reference to Disability Progression

Abstract

Background: We compared the magnetic resonance imaging (MRI) features between Japanese and Caucasian patients with multiple sclerosis (MS), and identified the relationships between MRI features and disability.

Methods: From the baseline data of phase II fingolimod trials, 95 Japanese and 246 Caucasian relapsing-remitting MS patients were enrolled. The number, volume, and distribution of brain MRI lesions were evaluated using T2-weighted (T2W) images. Cross-sectional total normalized brain volume (NBV), normalized cortical gray matter volume, normalized deep gray matter volume (NDGMV), normalized white matter volume (NWMV), and normalized thalamic volume were measured.

Results: Japanese patients had significantly lower Expanded Disability Status Scale (EDSS) scores than Caucasian patients (mean 2.0 vs. 2.3, p = 0.008), despite a similar disease duration. Japanese patients showed a trend towards fewer T2W-lesions (median 50 vs. 65, p = 0.08) and significantly lower frequencies of cerebellar and parietal lobe lesions (p = 0.02 for both) than Caucasian patients. There were no differences in T2W-lesion volume between races, whereas Japanese patients had a significantly larger T2W-lesion volume per lesion compared with Caucasian patients (median 140 mm vs. 85 mm, p < 0.0001). T2W-lesion volumes were positively correlated with EDSS scores in Japanese patients (p < 0.0001). In both races, NBV, normalized cortical gray matter volume, NDGMV, and thalamic volume were negatively correlated with disease duration and EDSS scores (p < 0.01 for all). NWMV was negatively correlated with disease duration and EDSS scores only in Caucasian patients (p = 0.03 and p = 0.004, respectively). NBV, NDGMV, NWMV, and thalamic volume were consistently smaller in Japanese compared with Caucasian patients throughout the entire examined disease duration (p = 0.046, p = 0.01, p = 0.005, and p = 0.04, respectively). Japanese patients had a significantly faster reduction in NDGMV (p = 0.001), particularly for thalamic volume (p = 0.001), with disease duration compared with Caucasian patients.

Conclusions: Gray matter atrophy is a common denominator for disability in Japanese and Caucasian patients. Additional contributory factors for disability include T2W-lesion volume in Japanese patients and white matter atrophy in Caucasian patients. Less frequent parietal and cerebellar involvement with fewer T2W-lesions may underlie milder disability in Japanese patients.

Citing Articles

Imaging phenotypic differences in multiple sclerosis: at the crossroads of aging, sex, race, and ethnicity.

Nathoo N, Neyal N, Kantarci O, Zeydan B Front Glob Womens Health. 2024; 5:1412482.

PMID: 39006184 PMC: 11245741. DOI: 10.3389/fgwh.2024.1412482.


Do magnetic resonance imaging features differ between persons with multiple sclerosis of various races and ethnicities?.

Nathoo N, Zeydan B, Neyal N, Chelf C, Okuda D, Kantarci O Front Neurol. 2023; 14:1215774.

PMID: 37448745 PMC: 10338060. DOI: 10.3389/fneur.2023.1215774.


Understanding humoral immunity and multiple sclerosis severity in Black, and Latinx patients.

Telesford K, Amezcua L, Tardo L, Horton L, Lund B, Reder A Front Immunol. 2023; 14:1172993.

PMID: 37215103 PMC: 10196635. DOI: 10.3389/fimmu.2023.1172993.


The effects of copper sulfate on the structure and function of the rat cerebellum: A stereological and behavioral study.

Erfanizadeh M, Noorafshan A, Naseh M, Karbalay-Doust S IBRO Neurosci Rep. 2021; 11:119-127.

PMID: 34604835 PMC: 8463771. DOI: 10.1016/j.ibneur.2021.09.001.


HLA genotype-clinical phenotype correlations in multiple sclerosis and neuromyelitis optica spectrum disorders based on Japan MS/NMOSD Biobank data.

Watanabe M, Nakamura Y, Sato S, Niino M, Fukaura H, Tanaka M Sci Rep. 2021; 11(1):607.

PMID: 33436735 PMC: 7804194. DOI: 10.1038/s41598-020-79833-7.


References
1.
Giess R, Pfuhl C, Behrens J, Rasche L, Freitag E, Khalighy N . Epstein-Barr virus antibodies in serum and DNA load in saliva are not associated with radiological or clinical disease activity in patients with early multiple sclerosis. PLoS One. 2017; 12(4):e0175279. PMC: 5384756. DOI: 10.1371/journal.pone.0175279. View

2.
Nakashima I, Fujihara K, Okita N, Takase S, Itoyama Y . Clinical and MRI study of brain stem and cerebellar involvement in Japanese patients with multiple sclerosis. J Neurol Neurosurg Psychiatry. 1999; 67(2):153-7. PMC: 1736498. DOI: 10.1136/jnnp.67.2.153. View

3.
Fisher E, Chang A, Fox R, Tkach J, Svarovsky T, Nakamura K . Imaging correlates of axonal swelling in chronic multiple sclerosis brains. Ann Neurol. 2007; 62(3):219-28. DOI: 10.1002/ana.21113. View

4.
Bergamaschi R . Prognosis of multiple sclerosis: clinical factors predicting the late evolution for an early treatment decision. Expert Rev Neurother. 2006; 6(3):357-64. DOI: 10.1586/14737175.6.3.357. View

5.
Giorgio A, Santelli L, Tomassini V, Bosnell R, Smith S, De Stefano N . Age-related changes in grey and white matter structure throughout adulthood. Neuroimage. 2010; 51(3):943-51. PMC: 2896477. DOI: 10.1016/j.neuroimage.2010.03.004. View