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Abstract Details

Clinical and Radiological Correlates of Multiple Sclerosis in patients of Middle Eastern and North African ancestry residing in Ontario, Canada.
Multiple Sclerosis
P4 - Poster Session 4 (5:30 PM-6:30 PM)
15-054
Our objective was to assess disease severity in Multiple Sclerosis(MS) patients immigrating to Canada from Middle Eastern and North African(MENA) countries.
The geographical distribution of MS is evolving, with rising incidence in low risk regions, including MENA countries. Evidence regarding disease severity in this population is conflicting. 

All MS patients originally from MENA countries(MENA-MS) were identified through the MS Clinic Registry of St. Michael’s Hospital in Toronto, Canada, which captures information on all clinic patients. Age and sex-matched MS patients of European descent(EUR-MS) were also identified. Sequential brain and cervical spine MRIs were reviewed for radiological activity. Disability progression was assessed by change in Expanded Disability Status Scale(EDSS) between first and last clinic visits and the Progression Index(PI).Overall disease severity was assessed by the MS Severity Score(MSSS). Student’s t-test and multivariable linear regression evaluated relationships between groups. 

192 MENA-MS and 192 EUR-MS patients were included. The mean age in both groups was 42.9 years and 67% were female. 25% and 24% of EUR-MS and MENA-MS had progressive disease, with mean disease duration of 11.5 and 11.43 years, respectively. Measures of clinical and radiological disease activity, including annualized relapse rate, baseline EDSS, and annual MRI disease activity did not differ. Disability progression was higher in MENA-MS (EDSS change=0.24 vs. 0.06,p=0.01) and MENA-MS showed greater disease severity with respect to MSSS(3.12 vs. 2.67,p=0.04) and PI(0.34 vs. 0.27,p=0.07).

MENA-MS patients demonstrate higher disease severity scores and greater disability progression compared to EUR-MS patients, despite that predominately “inflammatory” measures of disease activity, including relapse rate and MRI disease activity are similar. These findings suggest that MENA-MS patients may harbor a more aggressive disease phenotype with progression outside of relapses. Further evaluation of MS in patients of MENA descent is warranted, as there are implications for disease prognosis and management. 
Authors/Disclosures
Isobel A. Hawes (UCSF)
PRESENTER
Ms. Hawes has nothing to disclose.
Ashley Jones No disclosure on file
Melanie Guenette No disclosure on file
Jiwon Oh, MD, FAAN (St Michael's Hospital) Dr. Oh has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Roche. The institution of Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen-Idec. Dr. Oh has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for EMD-Serono. Dr. Oh has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi-Genzyme. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novartis. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Amgen. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for BMS. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Astra Zeneca. Dr. Oh has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Roche. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen-Idec. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi-Genzyme. The institution of Dr. Oh has received research support from Biogen-Idec. The institution of Dr. Oh has received research support from Roche.