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Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis

Multiple Sclerosis (MS) is a progressive neurodegenerative disease that affects more than 2 million people worldwide. Increasing knowledge about MS in different populations has advanced our understanding of disease epidemiology and variation in the natural history of MS among White and minority popu...

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Autores principales: Mercado, Vicki, Dongarwar, Deepa, Fisher, Kristen, Salihu, Hamisu M., Hutton, George J., Cuascut, Fernando X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760789/
https://www.ncbi.nlm.nih.gov/pubmed/33255552
http://dx.doi.org/10.3390/biomedicines8120534
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author Mercado, Vicki
Dongarwar, Deepa
Fisher, Kristen
Salihu, Hamisu M.
Hutton, George J.
Cuascut, Fernando X.
author_facet Mercado, Vicki
Dongarwar, Deepa
Fisher, Kristen
Salihu, Hamisu M.
Hutton, George J.
Cuascut, Fernando X.
author_sort Mercado, Vicki
collection PubMed
description Multiple Sclerosis (MS) is a progressive neurodegenerative disease that affects more than 2 million people worldwide. Increasing knowledge about MS in different populations has advanced our understanding of disease epidemiology and variation in the natural history of MS among White and minority populations. In addition to differences in incidence, African American (AA) and Hispanic patients have greater disease burden and disability in earlier stages of disease compared to White patients. To further characterize MS in AA and Hispanic populations, we conducted a retrospective chart analysis of 112 patients treated at an MS center in Houston, Texas. Here, we describe similarities and differences in clinical presentation, MRI findings, treatment regimens, disability progression, and relapse rate. While we found several similarities between the groups regarding mean age, disability severity, and degree of brain atrophy at diagnosis, we also describe a few divergences. Interestingly, we found that patients who were evaluated by a neurologist at symptom onset had significantly decreased odds of greater disability [defined as Expanded Disability Status Scale (EDSS) > 4.5] at last presentation compared to patients who were not evaluated by a neurologist (OR: 0.04, 95% CI: 0.16–0.9). We also found that active smokers had significantly increased odds of greater disability both at diagnosis and at last clinical encounter compared to nonsmokers (OR: 2.44, 95% CI: 1.10–7.10, OR= 2.44, 95% CI: 1.35–6.12, p = 0.01, respectively). Additionally, we observed significant differences in treatment adherence between groups. Assessment of the degree of brain atrophy and progression over time, along with an enumeration of T1, T2, and gadolinium-enhancing brain lesions, did not reveal differences across groups.
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spelling pubmed-77607892020-12-26 Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis Mercado, Vicki Dongarwar, Deepa Fisher, Kristen Salihu, Hamisu M. Hutton, George J. Cuascut, Fernando X. Biomedicines Article Multiple Sclerosis (MS) is a progressive neurodegenerative disease that affects more than 2 million people worldwide. Increasing knowledge about MS in different populations has advanced our understanding of disease epidemiology and variation in the natural history of MS among White and minority populations. In addition to differences in incidence, African American (AA) and Hispanic patients have greater disease burden and disability in earlier stages of disease compared to White patients. To further characterize MS in AA and Hispanic populations, we conducted a retrospective chart analysis of 112 patients treated at an MS center in Houston, Texas. Here, we describe similarities and differences in clinical presentation, MRI findings, treatment regimens, disability progression, and relapse rate. While we found several similarities between the groups regarding mean age, disability severity, and degree of brain atrophy at diagnosis, we also describe a few divergences. Interestingly, we found that patients who were evaluated by a neurologist at symptom onset had significantly decreased odds of greater disability [defined as Expanded Disability Status Scale (EDSS) > 4.5] at last presentation compared to patients who were not evaluated by a neurologist (OR: 0.04, 95% CI: 0.16–0.9). We also found that active smokers had significantly increased odds of greater disability both at diagnosis and at last clinical encounter compared to nonsmokers (OR: 2.44, 95% CI: 1.10–7.10, OR= 2.44, 95% CI: 1.35–6.12, p = 0.01, respectively). Additionally, we observed significant differences in treatment adherence between groups. Assessment of the degree of brain atrophy and progression over time, along with an enumeration of T1, T2, and gadolinium-enhancing brain lesions, did not reveal differences across groups. MDPI 2020-11-25 /pmc/articles/PMC7760789/ /pubmed/33255552 http://dx.doi.org/10.3390/biomedicines8120534 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mercado, Vicki
Dongarwar, Deepa
Fisher, Kristen
Salihu, Hamisu M.
Hutton, George J.
Cuascut, Fernando X.
Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis
title Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis
title_full Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis
title_fullStr Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis
title_full_unstemmed Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis
title_short Multiple Sclerosis in a Multi-Ethnic Population in Houston, Texas: A Retrospective Analysis
title_sort multiple sclerosis in a multi-ethnic population in houston, texas: a retrospective analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760789/
https://www.ncbi.nlm.nih.gov/pubmed/33255552
http://dx.doi.org/10.3390/biomedicines8120534
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