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Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies
BACKGROUND: The epidemiological evidence for a dose-response relationship between tea consumption and risk of cognitive disorders is sparse. The aim of the study was to summarize the evidence for the association of tea consumption with risk of cognitive disorders and assess the dose-response relatio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522147/ https://www.ncbi.nlm.nih.gov/pubmed/28496007 http://dx.doi.org/10.18632/oncotarget.17429 |
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author | Liu, Xueying Du, Xiaoyuan Han, Guanying Gao, Wenyuan |
author_facet | Liu, Xueying Du, Xiaoyuan Han, Guanying Gao, Wenyuan |
author_sort | Liu, Xueying |
collection | PubMed |
description | BACKGROUND: The epidemiological evidence for a dose-response relationship between tea consumption and risk of cognitive disorders is sparse. The aim of the study was to summarize the evidence for the association of tea consumption with risk of cognitive disorders and assess the dose-response relationship. METHODS: We searched electronic databases of Pubmed, Embase, and Cochrane Library (from 1965 to Jan 19, 2017) for eligible studies that published in the international journals. A random-effects model was used to pool the most adjusted odds ratios (ORs) and the corresponding 95% confidence intervals (CIs). RESULTS: Seventeen studies involving 48,435 participants were included in our study. The meta-analysis showed that a higher tea consumption was associated with a significant reduction in the risk of cognitive disorders (OR=0.73, 95% CI: 0.65-0.82). When considering the specific types of tea consumption, the significantly inverse association is only found in green tea consumption (OR=0.64, 95% CI: 0.53-0.77) but not in black/oolong tea consumption (OR=0.75, 95% CI: 0.55-1.01). Dose-response meta-analysis indicated that tea consumption is linearly associated with a reduced risk of cognitive disorders. An increment of 100 ml/day, 300 ml/day, and 500 ml/day of tea consumption was associated with a 6% (OR=0.94, 95% CI: 0.92-0.96), 19% (OR=0.81, 95% CI: 0.74-0.88), and 29% (OR=0.71, 95% CI: 0.62-0.82) lower risk of cognitive disorders. CONCLUSIONS: Tea consumption is inversely and linearly related to the risk of cognitive disorders. More studies are needed to further confirm our findings. |
format | Online Article Text |
id | pubmed-5522147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55221472017-08-08 Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies Liu, Xueying Du, Xiaoyuan Han, Guanying Gao, Wenyuan Oncotarget Meta-Analysis BACKGROUND: The epidemiological evidence for a dose-response relationship between tea consumption and risk of cognitive disorders is sparse. The aim of the study was to summarize the evidence for the association of tea consumption with risk of cognitive disorders and assess the dose-response relationship. METHODS: We searched electronic databases of Pubmed, Embase, and Cochrane Library (from 1965 to Jan 19, 2017) for eligible studies that published in the international journals. A random-effects model was used to pool the most adjusted odds ratios (ORs) and the corresponding 95% confidence intervals (CIs). RESULTS: Seventeen studies involving 48,435 participants were included in our study. The meta-analysis showed that a higher tea consumption was associated with a significant reduction in the risk of cognitive disorders (OR=0.73, 95% CI: 0.65-0.82). When considering the specific types of tea consumption, the significantly inverse association is only found in green tea consumption (OR=0.64, 95% CI: 0.53-0.77) but not in black/oolong tea consumption (OR=0.75, 95% CI: 0.55-1.01). Dose-response meta-analysis indicated that tea consumption is linearly associated with a reduced risk of cognitive disorders. An increment of 100 ml/day, 300 ml/day, and 500 ml/day of tea consumption was associated with a 6% (OR=0.94, 95% CI: 0.92-0.96), 19% (OR=0.81, 95% CI: 0.74-0.88), and 29% (OR=0.71, 95% CI: 0.62-0.82) lower risk of cognitive disorders. CONCLUSIONS: Tea consumption is inversely and linearly related to the risk of cognitive disorders. More studies are needed to further confirm our findings. Impact Journals LLC 2017-04-26 /pmc/articles/PMC5522147/ /pubmed/28496007 http://dx.doi.org/10.18632/oncotarget.17429 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Meta-Analysis Liu, Xueying Du, Xiaoyuan Han, Guanying Gao, Wenyuan Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies |
title | Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies |
title_full | Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies |
title_fullStr | Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies |
title_full_unstemmed | Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies |
title_short | Association between tea consumption and risk of cognitive disorders: A dose-response meta-analysis of observational studies |
title_sort | association between tea consumption and risk of cognitive disorders: a dose-response meta-analysis of observational studies |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522147/ https://www.ncbi.nlm.nih.gov/pubmed/28496007 http://dx.doi.org/10.18632/oncotarget.17429 |
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