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Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants

The present study examines how alcohol intake from wine and non-wine alcoholic beverages (non-wine) in g/d, as well as cups of coffee and tea included as continuous covariates and mutually adjusted are associated with all-cause, cancer, non-cancer and CVD mortality. Consumption was assessed in 354 3...

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Autores principales: Schaefer, Sylva M., Kaiser, Anna, Behrendt, Inken, Eichner, Gerrit, Fasshauer, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816653/
https://www.ncbi.nlm.nih.gov/pubmed/35109963
http://dx.doi.org/10.1017/S000711452200040X
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author Schaefer, Sylva M.
Kaiser, Anna
Behrendt, Inken
Eichner, Gerrit
Fasshauer, Mathias
author_facet Schaefer, Sylva M.
Kaiser, Anna
Behrendt, Inken
Eichner, Gerrit
Fasshauer, Mathias
author_sort Schaefer, Sylva M.
collection PubMed
description The present study examines how alcohol intake from wine and non-wine alcoholic beverages (non-wine) in g/d, as well as cups of coffee and tea included as continuous covariates and mutually adjusted are associated with all-cause, cancer, non-cancer and CVD mortality. Consumption was assessed in 354 386 participants of the UK Biobank cohort who drank alcohol at least occasionally and survived at least 2 years after baseline with 20 201 deaths occurring over 4·2 million person-years. Hazard ratios (HR) for mortality were assessed with Cox proportional hazard regression models and beverage intake fitted as penalised cubic splines. A significant U-shaped association was detected between wine consumption and all-cause, non-cancer and CVD mortality. Wine consumption with lowest risk of death (nadir) ranged from 19 to 23 g alcohol/d in all participants and both sexes separately. In contrast, non-wine intake was significantly and positively associated in a dose-dependent manner with all mortality types studied except for CVD in females and with the nadir between 0 and 12 g alcohol/d. In all participants, the nadir for all-cause mortality was 2 cups coffee/d with non-coffee drinkers showing a slightly increased risk of death. Tea consumption was significantly and negatively associated with all mortality types in both sexes. Taken together, light to moderate consumption of wine but not non-wine is associated with decreased all-cause and non-cancer mortality. A minor negative association of coffee consumption with mortality cannot be excluded whereas tea intake is associated with a consistently decreased risk of all mortality types studied.
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spelling pubmed-98166532023-01-18 Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants Schaefer, Sylva M. Kaiser, Anna Behrendt, Inken Eichner, Gerrit Fasshauer, Mathias Br J Nutr Research Article The present study examines how alcohol intake from wine and non-wine alcoholic beverages (non-wine) in g/d, as well as cups of coffee and tea included as continuous covariates and mutually adjusted are associated with all-cause, cancer, non-cancer and CVD mortality. Consumption was assessed in 354 386 participants of the UK Biobank cohort who drank alcohol at least occasionally and survived at least 2 years after baseline with 20 201 deaths occurring over 4·2 million person-years. Hazard ratios (HR) for mortality were assessed with Cox proportional hazard regression models and beverage intake fitted as penalised cubic splines. A significant U-shaped association was detected between wine consumption and all-cause, non-cancer and CVD mortality. Wine consumption with lowest risk of death (nadir) ranged from 19 to 23 g alcohol/d in all participants and both sexes separately. In contrast, non-wine intake was significantly and positively associated in a dose-dependent manner with all mortality types studied except for CVD in females and with the nadir between 0 and 12 g alcohol/d. In all participants, the nadir for all-cause mortality was 2 cups coffee/d with non-coffee drinkers showing a slightly increased risk of death. Tea consumption was significantly and negatively associated with all mortality types in both sexes. Taken together, light to moderate consumption of wine but not non-wine is associated with decreased all-cause and non-cancer mortality. A minor negative association of coffee consumption with mortality cannot be excluded whereas tea intake is associated with a consistently decreased risk of all mortality types studied. Cambridge University Press 2023-01-14 2022-02-03 /pmc/articles/PMC9816653/ /pubmed/35109963 http://dx.doi.org/10.1017/S000711452200040X Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Research Article
Schaefer, Sylva M.
Kaiser, Anna
Behrendt, Inken
Eichner, Gerrit
Fasshauer, Mathias
Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants
title Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants
title_full Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants
title_fullStr Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants
title_full_unstemmed Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants
title_short Association of alcohol types, coffee and tea intake with mortality: prospective cohort study of UK Biobank participants
title_sort association of alcohol types, coffee and tea intake with mortality: prospective cohort study of uk biobank participants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816653/
https://www.ncbi.nlm.nih.gov/pubmed/35109963
http://dx.doi.org/10.1017/S000711452200040X
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