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Abstract Details

African Americans with multiple sclerosis (MS) are more likely to have paramagnetic rim lesions (PRLs) compared to Caucasians
Multiple Sclerosis
P11 - Poster Session 11 (11:45 AM-12:45 PM)
3-017

To determine the prevalence of paramagnetic rim lesions (PRLs) in African American patients with multiple sclerosis (AAwMS) compared to Caucasian (CAwMS).

 

PRLs are a subset of chronic active MS lesions with a rim of iron-laden innate immune cells and their presence has been associated with higher disability. AAwMS have been clinically observed to have higher disability and more severe symptoms as compared to other racial groups.

In this retrospective study of 139 AAwMS and 132 CAwMS quantitative susceptibility mapping (QSM), an MRI approach sensitive to iron, was used to identify PRLs. A linear model assessed the relationship between EDSS and race, adjusting for total lesion number (TLN), sex, age and disease duration (DD). The association of PRL per patient and race was modeled, adjusting for clinical variables and total lesions, using a zero-inflated Poisson regression.

The cohorts were well matched on all clinical variables and TLN. In a linear model, AAwMS had a higher EDSS (p-value <0.001) with, on average, a 1.16-point higher EDSS (95% CI: [0.73, 1.60] than CAwMS. AAwMS had a mean of 1.3 (2.72) PRL whereas CAwMS had 0.82 (1.69), p=0.085. In the zero-inflated Poisson model, the log odds ratio of having no PRL was 0.53 (95% CI: [0.29, 0.97], p-value = 0.039) for AAwMS, indicating more patients have at least one PRL. In the Poisson model, only TLN (p = 0.021) and gender (p = 0.046) were found to be significant, which indicates that AAwMS were more likely to have one PRL, however among all patients with PRL, the total number of PRL did not depend on race.  

 

This is the first study to explore racial differences in the occurrence of chronic active lesions and provides preliminary evidence that PRL could relate to racial specific differences in disease pathology, an area which has been significantly understudied.

Authors/Disclosures
Nara Michaelson, MD (Beth Israel Deaconess Medical Center)
PRESENTER
The institution of Dr. Michaelson has received research support from Biogen. The institution of Dr. Michaelson has received research support from the National Multiple Sclerosis Society (NMSS). Dr. Michaelson has received research support from Sanofi.
Melanie Marcille (University of Florida) Ms. Marcille has nothing to disclose.
No disclosure on file
Ulrike Kaunzner, MD (Weill-Cornell) Dr. Kaunzner has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Kaunzner has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Medlearning.
No disclosure on file
Nancy M. Nealon, MD (Cornell Medical Center) Dr. Nealon has nothing to disclose.
Thanh Nguyen No disclosure on file
Susan Gauthier, DO (Weill Cornell Medicine) Dr. Gauthier has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen. Dr. Gauthier has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Gauthier has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. The institution of Dr. Gauthier has received research support from Genentech.