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Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study
BACKGROUND: The incidence of multiple sclerosis (MS) changes from generation to generation in ethnically different immigrants compared with native-born people. We aimed to determine whether there are generational changes in MS phenotypes among North African immigrants in France. METHODS: Cohort stud...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870962/ https://www.ncbi.nlm.nih.gov/pubmed/29584762 http://dx.doi.org/10.1371/journal.pone.0194115 |
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author | Nardin, Clotilde Latarche, Clotilde Soudant, Marc Dahan, Camille Michaud, Maud Pittion-Vouyovitch, Sophie Guillemin, Francis Debouverie, Marc Mathey, Guillaume |
author_facet | Nardin, Clotilde Latarche, Clotilde Soudant, Marc Dahan, Camille Michaud, Maud Pittion-Vouyovitch, Sophie Guillemin, Francis Debouverie, Marc Mathey, Guillaume |
author_sort | Nardin, Clotilde |
collection | PubMed |
description | BACKGROUND: The incidence of multiple sclerosis (MS) changes from generation to generation in ethnically different immigrants compared with native-born people. We aimed to determine whether there are generational changes in MS phenotypes among North African immigrants in France. METHODS: Cohort study with data from a population-based MS registry to compare the clinical characteristics of 80 first (NAG1) and 167 second (NAG2) generation North Africans with MS living in France with 5200 native-born Europeans. Adjusted Cox models were used to test the association between scores of 3 and 6 on the expanded disability status scale (EDSS) and the “origin/generation” variable. RESULTS: Cox models for EDSS scores 3 and 6 showed a higher risk of score 3 (hazard ratio = 1.738, 95% confidence interval 1.237 to 2.444; P = .002) and 6 (hazard ratio = 2.372, 95% confidence interval 1.626 to 3.462; P<.0001) for NAG1 than Europeans. Being NAG2 was not significantly associated with higher hazards of scores 3 and 6. CONCLUSIONS: We found two different phenotypes among NAG1 and NAG2 MS patients in France. NAG1, but not NAG2, have a higher risk of disability than Europeans. This raises the question of environmental factors in MS expression, and advocates appropriate patient management according to generation in immigrants. |
format | Online Article Text |
id | pubmed-5870962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58709622018-04-06 Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study Nardin, Clotilde Latarche, Clotilde Soudant, Marc Dahan, Camille Michaud, Maud Pittion-Vouyovitch, Sophie Guillemin, Francis Debouverie, Marc Mathey, Guillaume PLoS One Research Article BACKGROUND: The incidence of multiple sclerosis (MS) changes from generation to generation in ethnically different immigrants compared with native-born people. We aimed to determine whether there are generational changes in MS phenotypes among North African immigrants in France. METHODS: Cohort study with data from a population-based MS registry to compare the clinical characteristics of 80 first (NAG1) and 167 second (NAG2) generation North Africans with MS living in France with 5200 native-born Europeans. Adjusted Cox models were used to test the association between scores of 3 and 6 on the expanded disability status scale (EDSS) and the “origin/generation” variable. RESULTS: Cox models for EDSS scores 3 and 6 showed a higher risk of score 3 (hazard ratio = 1.738, 95% confidence interval 1.237 to 2.444; P = .002) and 6 (hazard ratio = 2.372, 95% confidence interval 1.626 to 3.462; P<.0001) for NAG1 than Europeans. Being NAG2 was not significantly associated with higher hazards of scores 3 and 6. CONCLUSIONS: We found two different phenotypes among NAG1 and NAG2 MS patients in France. NAG1, but not NAG2, have a higher risk of disability than Europeans. This raises the question of environmental factors in MS expression, and advocates appropriate patient management according to generation in immigrants. Public Library of Science 2018-03-27 /pmc/articles/PMC5870962/ /pubmed/29584762 http://dx.doi.org/10.1371/journal.pone.0194115 Text en © 2018 Nardin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Nardin, Clotilde Latarche, Clotilde Soudant, Marc Dahan, Camille Michaud, Maud Pittion-Vouyovitch, Sophie Guillemin, Francis Debouverie, Marc Mathey, Guillaume Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study |
title | Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study |
title_full | Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study |
title_fullStr | Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study |
title_full_unstemmed | Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study |
title_short | Generational changes in multiple sclerosis phenotype in North African immigrants in France: A population-based observational study |
title_sort | generational changes in multiple sclerosis phenotype in north african immigrants in france: a population-based observational study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870962/ https://www.ncbi.nlm.nih.gov/pubmed/29584762 http://dx.doi.org/10.1371/journal.pone.0194115 |
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