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The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation
Our aim was to identify whether low-grade inflammation, reflected by C-reactive protein (CRP), explains the higher risk for incident type 2 diabetes (T2D) among ethnic minorities. We included 837 Dutch, 712 South-Asian Surinamese, 797 African Surinamese, 804 Ghanaian, 817 Turkish and 778 Moroccan or...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934847/ https://www.ncbi.nlm.nih.gov/pubmed/31882814 http://dx.doi.org/10.1038/s41598-019-56596-4 |
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author | Muilwijk, Mirthe Nieuwdorp, Max Snijder, Marieke B. Hof, Michel H. P. Stronks, Karien van Valkengoed, Irene G. M. |
author_facet | Muilwijk, Mirthe Nieuwdorp, Max Snijder, Marieke B. Hof, Michel H. P. Stronks, Karien van Valkengoed, Irene G. M. |
author_sort | Muilwijk, Mirthe |
collection | PubMed |
description | Our aim was to identify whether low-grade inflammation, reflected by C-reactive protein (CRP), explains the higher risk for incident type 2 diabetes (T2D) among ethnic minorities. We included 837 Dutch, 712 South-Asian Surinamese, 797 African Surinamese, 804 Ghanaian, 817 Turkish and 778 Moroccan origin participants of the HELIUS study (Amsterdam, the Netherlands). We used multiple linear regression to assess ethnic differences in CRP levels. We determined the association of CRP with T2D and the modifying effect of ethnicity by cox regression, and compared hazard ratios for the association between ethnicity and T2D before and after adjustment for CRP. CRP levels were higher in ethnic minority groups than in Dutch origin participants. CRP was associated with a higher T2D incidence, similarly across ethnic groups (overall HR per SD 1.38 [95% CI 1.14; 1.68]). However, the association was attenuated and no longer statistically significant after adjustment for adiposity measures (HR 1.11 [95% CI 0.90; 1.37]). CRP accounted for a very small part of the ethnic differences in T2D, but only in models unadjusted for adiposity. Low-grade inflammation does not substantially contribute to the higher risk of T2D among ethnic minority populations compared to the Dutch. |
format | Online Article Text |
id | pubmed-6934847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69348472019-12-31 The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation Muilwijk, Mirthe Nieuwdorp, Max Snijder, Marieke B. Hof, Michel H. P. Stronks, Karien van Valkengoed, Irene G. M. Sci Rep Article Our aim was to identify whether low-grade inflammation, reflected by C-reactive protein (CRP), explains the higher risk for incident type 2 diabetes (T2D) among ethnic minorities. We included 837 Dutch, 712 South-Asian Surinamese, 797 African Surinamese, 804 Ghanaian, 817 Turkish and 778 Moroccan origin participants of the HELIUS study (Amsterdam, the Netherlands). We used multiple linear regression to assess ethnic differences in CRP levels. We determined the association of CRP with T2D and the modifying effect of ethnicity by cox regression, and compared hazard ratios for the association between ethnicity and T2D before and after adjustment for CRP. CRP levels were higher in ethnic minority groups than in Dutch origin participants. CRP was associated with a higher T2D incidence, similarly across ethnic groups (overall HR per SD 1.38 [95% CI 1.14; 1.68]). However, the association was attenuated and no longer statistically significant after adjustment for adiposity measures (HR 1.11 [95% CI 0.90; 1.37]). CRP accounted for a very small part of the ethnic differences in T2D, but only in models unadjusted for adiposity. Low-grade inflammation does not substantially contribute to the higher risk of T2D among ethnic minority populations compared to the Dutch. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934847/ /pubmed/31882814 http://dx.doi.org/10.1038/s41598-019-56596-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Muilwijk, Mirthe Nieuwdorp, Max Snijder, Marieke B. Hof, Michel H. P. Stronks, Karien van Valkengoed, Irene G. M. The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
title | The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
title_full | The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
title_fullStr | The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
title_full_unstemmed | The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
title_short | The high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
title_sort | high risk for type 2 diabetes among ethnic minority populations is not explained by low-grade inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934847/ https://www.ncbi.nlm.nih.gov/pubmed/31882814 http://dx.doi.org/10.1038/s41598-019-56596-4 |
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