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Abstract Details

Multimodal Imaging in Black and White People with Multiple Sclerosis on Ocrelizumab: A Pilot Study
Multiple Sclerosis
P3 - Poster Session 3 (11:45 AM-12:45 PM)
1-012
We investigated the differences in the impact of ocrelizumab on AMRIMs between black and white pwMS over a 12-month follow-up period.

Studies comparing ocrelizumab’s effects on advanced magnetic resonance imaging metrics (AMRIMs) between black and white people with multiple sclerosis (pwMS) are limited. AMRIMs, including magnetization transfer ratio (MTR), fractional anisotropy (FA), mean diffusivity (MD), and the ratio of total N-acetyl-aspartate concentration/total creatine concentration (tNAA/tCr) using proton magnetic resonance spectroscopy (1H-MRS), assess brain pathology in MS.

Twelve pwMS had brain MRIs at baseline and month 12 on a SIEMENS 3T Verio system and were started on ocrelizumab at baseline. Mann-Whitney U test in SPSS v29 was used to assess AMRIM differences between Black and White patients over 12 months, with p<0.05 as significant.

The median age of black pwMS (n=6) was 37.7 years±6.2, and white (n=6) was 46.8 years±10.5 (p=0.128).  Mean change in the MTR of normal-appearing white matter (NAWM) from baseline to month 12 was significantly different between black (-0.56%±1) and white pwMS (1.04%±0.98)  (p=0.02). On the contrary, mean change in MTR in normal-appearing grey matter (NAGM) from baseline to month 12 was non-significant, -0.4%±1.5 in black and 1.2%±1.1 in white pwMS. In MS lesions, mean MTR change in blacks was 1.7%±1.3 and whites 2.4%±1.8, the mean FA change in blacks was 0.06±0.03 and whites 0.03±0.03, and the mean MD change in blacks was -0.04 x10-3 mm2/s ±0.04 and whites -0.06 x10-3 mm2/s ±0.06. Mean change in WM tNAA/tCr from baseline to month 12 was 0.06±0.1 in blacks and 0.05±0.1 in whites. No significant difference in the mean change in FA and MD in NAGM and NAWM between the two groups.

Our small sample suggests ocrelizumab may impact NAWM MTR differently in Black and White pwMS. Larger studies with extended follow-up are needed to explore potential differences in AMRIMs.

 

Authors/Disclosures
Carla E. Santiago-Martinez (Wayne State University)
PRESENTER
Ms. Santiago-Martinez has nothing to disclose.
Muhammad F. Raghib, MD (Wayne State University) Dr. Raghib has nothing to disclose.
Fen Bao Fen Bao has nothing to disclose.
Eman Dannawey (Wayne State University) Eman Dannawey has nothing to disclose.
ZL Liaquat (Wayne State University) ZL Liaquat has nothing to disclose.
Zahid Latif, Imaging Technologist Mr. Latif has nothing to disclose.
Idan Hannawa, PharmD, BCPS Mr. Hannawa has received personal compensation for serving as an employee of Genentech. Mr. Hannawa has stock in Genentech.
Rajshi Gandhi, MPH, MSc Mrs. Gandhi has nothing to disclose.
David Clayton David Clayton has received personal compensation for serving as an employee of Genentech/Roche. David Clayton has received stock or an ownership interest from Roche. An immediate family member of David Clayton has received publishing royalties from a publication relating to health care.
Ajibola Abioye (Genentech) Ajibola Abioye has received personal compensation for serving as an employee of Genentech, Inc.
Jacob C. Rube, MD (University Health Center) Dr. Rube has nothing to disclose.
Evanthia Bernitsas, MD, FAAN (Wayne State School of Medicine) Dr. Bernitsas has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Amgen. Dr. Bernitsas has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Vanda. The institution of Dr. Bernitsas has received research support from Roche/Genentech.