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Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups
AIM: To summarise the current literature and define patterns of disease in migrant and racial groups. METHODS: A structured key word search in Ovid Medline and EMBASE was undertaken in accordance with PRISMA guidelines. Studies on incidence, prevalence and disease phenotype of migrants and races com...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776404/ https://www.ncbi.nlm.nih.gov/pubmed/29391765 http://dx.doi.org/10.3748/wjg.v24.i3.424 |
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author | Misra, Ravi Faiz, Omar Munkholm, Pia Burisch, Johan Arebi, Naila |
author_facet | Misra, Ravi Faiz, Omar Munkholm, Pia Burisch, Johan Arebi, Naila |
author_sort | Misra, Ravi |
collection | PubMed |
description | AIM: To summarise the current literature and define patterns of disease in migrant and racial groups. METHODS: A structured key word search in Ovid Medline and EMBASE was undertaken in accordance with PRISMA guidelines. Studies on incidence, prevalence and disease phenotype of migrants and races compared with indigenous groups were eligible for inclusion. RESULTS: Thirty-three studies met the inclusion criteria. Individual studies showed significant differences in incidence, prevalence and disease phenotype between migrants or race and indigenous groups. Pooled analysis could only be undertaken for incidence studies on South Asians where there was significant heterogeneity between the studies [95% for ulcerative colitis (UC), 83% for Crohn’s disease (CD)]. The difference between incidence rates was not significant with a rate ratio South Asian: Caucasian of 0.78 (95%CI: 0.22-2.78) for CD and 1.39 (95%CI: 0.84-2.32) for UC. South Asians showed consistently higher incidence and more extensive UC than the indigenous population in five countries. A similar pattern was observed for Hispanics in the United States. Bangladeshis and African Americans showed an increased risk of CD with perianal disease. CONCLUSION: This review suggests that migration and race influence the risk of developing inflammatory bowel disease. This may be due to different inherent responses upon exposure to an environmental trigger in the adopted country. Further prospective studies on homogenous migrant populations are needed to validate these observations, with a parallel arm for in-depth investigation of putative drivers. |
format | Online Article Text |
id | pubmed-5776404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-57764042018-02-01 Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups Misra, Ravi Faiz, Omar Munkholm, Pia Burisch, Johan Arebi, Naila World J Gastroenterol Systematic Reviews AIM: To summarise the current literature and define patterns of disease in migrant and racial groups. METHODS: A structured key word search in Ovid Medline and EMBASE was undertaken in accordance with PRISMA guidelines. Studies on incidence, prevalence and disease phenotype of migrants and races compared with indigenous groups were eligible for inclusion. RESULTS: Thirty-three studies met the inclusion criteria. Individual studies showed significant differences in incidence, prevalence and disease phenotype between migrants or race and indigenous groups. Pooled analysis could only be undertaken for incidence studies on South Asians where there was significant heterogeneity between the studies [95% for ulcerative colitis (UC), 83% for Crohn’s disease (CD)]. The difference between incidence rates was not significant with a rate ratio South Asian: Caucasian of 0.78 (95%CI: 0.22-2.78) for CD and 1.39 (95%CI: 0.84-2.32) for UC. South Asians showed consistently higher incidence and more extensive UC than the indigenous population in five countries. A similar pattern was observed for Hispanics in the United States. Bangladeshis and African Americans showed an increased risk of CD with perianal disease. CONCLUSION: This review suggests that migration and race influence the risk of developing inflammatory bowel disease. This may be due to different inherent responses upon exposure to an environmental trigger in the adopted country. Further prospective studies on homogenous migrant populations are needed to validate these observations, with a parallel arm for in-depth investigation of putative drivers. Baishideng Publishing Group Inc 2018-01-21 2018-01-21 /pmc/articles/PMC5776404/ /pubmed/29391765 http://dx.doi.org/10.3748/wjg.v24.i3.424 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Systematic Reviews Misra, Ravi Faiz, Omar Munkholm, Pia Burisch, Johan Arebi, Naila Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
title | Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
title_full | Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
title_fullStr | Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
title_full_unstemmed | Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
title_short | Epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
title_sort | epidemiology of inflammatory bowel disease in racial and ethnic migrant groups |
topic | Systematic Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776404/ https://www.ncbi.nlm.nih.gov/pubmed/29391765 http://dx.doi.org/10.3748/wjg.v24.i3.424 |
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