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Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study

BACKGROUND: Higher coffee consumption has been associated with a lower risk of type 2 diabetes in cohort studies, but the physiological pathways through which coffee affects glucose metabolism are not fully understood. The aim of this study was to evaluate the associations between habitual coffee an...

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Autores principales: Rebello, Salome A, Chen, Cynthia H, Naidoo, Nasheen, Xu, Wang, Lee, Jeannette, Chia, Kee Seng, Tai, E Shyong, van Dam, Rob M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130641/
https://www.ncbi.nlm.nih.gov/pubmed/21631956
http://dx.doi.org/10.1186/1475-2891-10-61
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author Rebello, Salome A
Chen, Cynthia H
Naidoo, Nasheen
Xu, Wang
Lee, Jeannette
Chia, Kee Seng
Tai, E Shyong
van Dam, Rob M
author_facet Rebello, Salome A
Chen, Cynthia H
Naidoo, Nasheen
Xu, Wang
Lee, Jeannette
Chia, Kee Seng
Tai, E Shyong
van Dam, Rob M
author_sort Rebello, Salome A
collection PubMed
description BACKGROUND: Higher coffee consumption has been associated with a lower risk of type 2 diabetes in cohort studies, but the physiological pathways through which coffee affects glucose metabolism are not fully understood. The aim of this study was to evaluate the associations between habitual coffee and tea consumption and glucose metabolism in a multi-ethnic Asian population and possible mediation by inflammation. METHODS: We cross-sectionally examined the association between coffee, green tea, black tea and Oolong tea consumption and glycemic (fasting plasma glucose, HOMA-IR, HOMA-beta, plasma HbA1c) and inflammatory (plasma adiponectin and C-reactive protein) markers in a multi-ethnic Asian population (N = 4139). RESULTS: After adjusting for multiple confounders, we observed inverse associations between coffee and HOMA-IR (percent difference: - 8.8% for ≥ 3 cups/day versus rarely or never; P(trend )= 0.007), but no significant associations between coffee and inflammatory markers. Tea consumption was not associated with glycemic markers, but green tea was inversely associated with plasma C-reactive protein concentrations (percent difference: - 12.2% for ≥ 1 cup/day versus < 1 cup/week; P(trend )= 0.042). CONCLUSIONS: These data provide additional evidence for a beneficial effect of habitual caffeinated coffee consumption on insulin sensitivity, and suggest that this effect is unlikely to be mediated by anti-inflammatory mechanisms.
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spelling pubmed-31306412011-07-07 Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study Rebello, Salome A Chen, Cynthia H Naidoo, Nasheen Xu, Wang Lee, Jeannette Chia, Kee Seng Tai, E Shyong van Dam, Rob M Nutr J Research BACKGROUND: Higher coffee consumption has been associated with a lower risk of type 2 diabetes in cohort studies, but the physiological pathways through which coffee affects glucose metabolism are not fully understood. The aim of this study was to evaluate the associations between habitual coffee and tea consumption and glucose metabolism in a multi-ethnic Asian population and possible mediation by inflammation. METHODS: We cross-sectionally examined the association between coffee, green tea, black tea and Oolong tea consumption and glycemic (fasting plasma glucose, HOMA-IR, HOMA-beta, plasma HbA1c) and inflammatory (plasma adiponectin and C-reactive protein) markers in a multi-ethnic Asian population (N = 4139). RESULTS: After adjusting for multiple confounders, we observed inverse associations between coffee and HOMA-IR (percent difference: - 8.8% for ≥ 3 cups/day versus rarely or never; P(trend )= 0.007), but no significant associations between coffee and inflammatory markers. Tea consumption was not associated with glycemic markers, but green tea was inversely associated with plasma C-reactive protein concentrations (percent difference: - 12.2% for ≥ 1 cup/day versus < 1 cup/week; P(trend )= 0.042). CONCLUSIONS: These data provide additional evidence for a beneficial effect of habitual caffeinated coffee consumption on insulin sensitivity, and suggest that this effect is unlikely to be mediated by anti-inflammatory mechanisms. BioMed Central 2011-06-02 /pmc/articles/PMC3130641/ /pubmed/21631956 http://dx.doi.org/10.1186/1475-2891-10-61 Text en Copyright ©2011 Rebello et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Rebello, Salome A
Chen, Cynthia H
Naidoo, Nasheen
Xu, Wang
Lee, Jeannette
Chia, Kee Seng
Tai, E Shyong
van Dam, Rob M
Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study
title Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study
title_full Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study
title_fullStr Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study
title_full_unstemmed Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study
title_short Coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic Asian population: a cross-sectional study
title_sort coffee and tea consumption in relation to inflammation and basal glucose metabolism in a multi-ethnic asian population: a cross-sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130641/
https://www.ncbi.nlm.nih.gov/pubmed/21631956
http://dx.doi.org/10.1186/1475-2891-10-61
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