Multiple sclerosis in First Nations Canadians: A pilot comparison study

Background Genetic and clinical characteristics associated with multiple sclerosis (MS) may differ by ethnicity but few studies have evaluated whether characteristics of MS differ between individuals according to First Nations (FN) ethnicity. Objective Using a cross-sectional observational design, w...

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Published in:Multiple Sclerosis Journal - Experimental, Translational and Clinical
Main Authors: Marrie, Ruth Ann, Hall, Nicholas, Sadovnick, A Dessa
Format: Article in Journal/Newspaper
Language:English
Published: SAGE Publications 2016
Subjects:
Online Access:http://dx.doi.org/10.1177/2055217316666093
http://journals.sagepub.com/doi/pdf/10.1177/2055217316666093
http://journals.sagepub.com/doi/full-xml/10.1177/2055217316666093
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spelling crsagepubl:10.1177/2055217316666093 2024-04-28T08:19:01+00:00 Multiple sclerosis in First Nations Canadians: A pilot comparison study Marrie, Ruth Ann Hall, Nicholas Sadovnick, A Dessa 2016 http://dx.doi.org/10.1177/2055217316666093 http://journals.sagepub.com/doi/pdf/10.1177/2055217316666093 http://journals.sagepub.com/doi/full-xml/10.1177/2055217316666093 en eng SAGE Publications http://journals.sagepub.com/page/policies/text-and-data-mining-license Multiple Sclerosis Journal - Experimental, Translational and Clinical volume 2, page 205521731666609 ISSN 2055-2173 2055-2173 Cellular and Molecular Neuroscience Neurology (clinical) journal-article 2016 crsagepubl https://doi.org/10.1177/2055217316666093 2024-04-02T08:13:49Z Background Genetic and clinical characteristics associated with multiple sclerosis (MS) may differ by ethnicity but few studies have evaluated whether characteristics of MS differ between individuals according to First Nations (FN) ethnicity. Objective Using a cross-sectional observational design, we compared clinical and genetic characteristics between people with MS of FN and non-FN ethnicity. Methods We recruited participants of FN ethnicity with MS. We conducted a medical records review for each participant followed by a standardized interview and drawing of blood samples. The blood underwent genetic analyses for several HLA alleles. We compared the study sample with 127 non-FN MS participants from another study conducted in the same region using the same data collection procedures. Results We included 144 participants with MS, of whom 17 (11.8%) self-identified as FN. The age of symptom onset was earlier and the diagnostic delay shorter among FN participants although these differences did not reach statistical significance. As compared to non-FN participants, FN participants with MS had increased odds of comorbid psychiatric disease (OR 5.38; 95% CI: 1.84–15.8), and were less likely to be HLA-DRB1*1501 positive (OR 0.32; 95% CI: 0.11–0.96). Conclusion Genetic and clinical characteristics of MS differ among Canadians of FN and non-FN ethnicity. Article in Journal/Newspaper First Nations SAGE Publications Multiple Sclerosis Journal - Experimental, Translational and Clinical 2 205521731666609
institution Open Polar
collection SAGE Publications
op_collection_id crsagepubl
language English
topic Cellular and Molecular Neuroscience
Neurology (clinical)
spellingShingle Cellular and Molecular Neuroscience
Neurology (clinical)
Marrie, Ruth Ann
Hall, Nicholas
Sadovnick, A Dessa
Multiple sclerosis in First Nations Canadians: A pilot comparison study
topic_facet Cellular and Molecular Neuroscience
Neurology (clinical)
description Background Genetic and clinical characteristics associated with multiple sclerosis (MS) may differ by ethnicity but few studies have evaluated whether characteristics of MS differ between individuals according to First Nations (FN) ethnicity. Objective Using a cross-sectional observational design, we compared clinical and genetic characteristics between people with MS of FN and non-FN ethnicity. Methods We recruited participants of FN ethnicity with MS. We conducted a medical records review for each participant followed by a standardized interview and drawing of blood samples. The blood underwent genetic analyses for several HLA alleles. We compared the study sample with 127 non-FN MS participants from another study conducted in the same region using the same data collection procedures. Results We included 144 participants with MS, of whom 17 (11.8%) self-identified as FN. The age of symptom onset was earlier and the diagnostic delay shorter among FN participants although these differences did not reach statistical significance. As compared to non-FN participants, FN participants with MS had increased odds of comorbid psychiatric disease (OR 5.38; 95% CI: 1.84–15.8), and were less likely to be HLA-DRB1*1501 positive (OR 0.32; 95% CI: 0.11–0.96). Conclusion Genetic and clinical characteristics of MS differ among Canadians of FN and non-FN ethnicity.
format Article in Journal/Newspaper
author Marrie, Ruth Ann
Hall, Nicholas
Sadovnick, A Dessa
author_facet Marrie, Ruth Ann
Hall, Nicholas
Sadovnick, A Dessa
author_sort Marrie, Ruth Ann
title Multiple sclerosis in First Nations Canadians: A pilot comparison study
title_short Multiple sclerosis in First Nations Canadians: A pilot comparison study
title_full Multiple sclerosis in First Nations Canadians: A pilot comparison study
title_fullStr Multiple sclerosis in First Nations Canadians: A pilot comparison study
title_full_unstemmed Multiple sclerosis in First Nations Canadians: A pilot comparison study
title_sort multiple sclerosis in first nations canadians: a pilot comparison study
publisher SAGE Publications
publishDate 2016
url http://dx.doi.org/10.1177/2055217316666093
http://journals.sagepub.com/doi/pdf/10.1177/2055217316666093
http://journals.sagepub.com/doi/full-xml/10.1177/2055217316666093
genre First Nations
genre_facet First Nations
op_source Multiple Sclerosis Journal - Experimental, Translational and Clinical
volume 2, page 205521731666609
ISSN 2055-2173 2055-2173
op_rights http://journals.sagepub.com/page/policies/text-and-data-mining-license
op_doi https://doi.org/10.1177/2055217316666093
container_title Multiple Sclerosis Journal - Experimental, Translational and Clinical
container_volume 2
container_start_page 205521731666609
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