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The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study
CONTEXT: The role of alcohol intake in influencing longitudinal trajectories of adiponectin is unclear. OBJECTIVE: The objective of the study was to examine the association between alcohol intake and changes in the circulating levels of adiponectin over repeat measures. DESIGN, SETTING, AND PARTICIP...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490299/ https://www.ncbi.nlm.nih.gov/pubmed/26000546 http://dx.doi.org/10.1210/jc.2015-1845 |
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author | Bell, Steven Britton, Annie |
author_facet | Bell, Steven Britton, Annie |
author_sort | Bell, Steven |
collection | PubMed |
description | CONTEXT: The role of alcohol intake in influencing longitudinal trajectories of adiponectin is unclear. OBJECTIVE: The objective of the study was to examine the association between alcohol intake and changes in the circulating levels of adiponectin over repeat measures. DESIGN, SETTING, AND PARTICIPANTS: A prospective cohort study of 2855 men and women (74% men with a mean age of 50 y at baseline) drawn from the Whitehall II study. Data from study phases 3 (1991–1993), 5 (1997–1999), and 7 (2002–2004) were used. MAIN OUTCOME MEASURE: Adiponectin serum concentrations (nanograms per milliliter) were measured, and alcohol intake was defined in terms of number of UK units (1 U = 8 g ethanol) consumed in the previous 7 days on three occasions. Cross-sectional associations between alcohol and adiponectin levels were calculated using linear regression. A bivariate dual-change score model was used to estimate the effect of alcohol intake on upcoming change in adiponectin. Models were adjusted for age, sex, ethnicity, and smoking status. RESULTS: Alcohol consumption was cross-sectionally associated with (log transformed) adiponectin levels (β ranging from .001 to .004, depending on phase and level of adjustment) but was not associated with changes in adiponectin levels over time [γ = −0.002 (SE 0.002), P = 0.246]. CONCLUSION: Alcohol intake is not associated with changes in circulating adiponectin levels in this cohort. This finding provides evidence that adiponectin levels are unlikely to mediate the relationship between moderate alcohol consumption and reduced risk of type 2 diabetes. It is important to consider dynamic longitudinal relationships rather than cross-sectional associations. |
format | Online Article Text |
id | pubmed-4490299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44902992015-07-28 The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study Bell, Steven Britton, Annie J Clin Endocrinol Metab Original Articles CONTEXT: The role of alcohol intake in influencing longitudinal trajectories of adiponectin is unclear. OBJECTIVE: The objective of the study was to examine the association between alcohol intake and changes in the circulating levels of adiponectin over repeat measures. DESIGN, SETTING, AND PARTICIPANTS: A prospective cohort study of 2855 men and women (74% men with a mean age of 50 y at baseline) drawn from the Whitehall II study. Data from study phases 3 (1991–1993), 5 (1997–1999), and 7 (2002–2004) were used. MAIN OUTCOME MEASURE: Adiponectin serum concentrations (nanograms per milliliter) were measured, and alcohol intake was defined in terms of number of UK units (1 U = 8 g ethanol) consumed in the previous 7 days on three occasions. Cross-sectional associations between alcohol and adiponectin levels were calculated using linear regression. A bivariate dual-change score model was used to estimate the effect of alcohol intake on upcoming change in adiponectin. Models were adjusted for age, sex, ethnicity, and smoking status. RESULTS: Alcohol consumption was cross-sectionally associated with (log transformed) adiponectin levels (β ranging from .001 to .004, depending on phase and level of adjustment) but was not associated with changes in adiponectin levels over time [γ = −0.002 (SE 0.002), P = 0.246]. CONCLUSION: Alcohol intake is not associated with changes in circulating adiponectin levels in this cohort. This finding provides evidence that adiponectin levels are unlikely to mediate the relationship between moderate alcohol consumption and reduced risk of type 2 diabetes. It is important to consider dynamic longitudinal relationships rather than cross-sectional associations. Endocrine Society 2015-07 2015-05-22 /pmc/articles/PMC4490299/ /pubmed/26000546 http://dx.doi.org/10.1210/jc.2015-1845 Text en This article has been published under the terms of the Creative Commons Attribution License (CC-BY; https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s). |
spellingShingle | Original Articles Bell, Steven Britton, Annie The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study |
title | The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study |
title_full | The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study |
title_fullStr | The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study |
title_full_unstemmed | The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study |
title_short | The Role of Alcohol Consumption in Regulating Circulating Levels of Adiponectin: A Prospective Cohort Study |
title_sort | role of alcohol consumption in regulating circulating levels of adiponectin: a prospective cohort study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490299/ https://www.ncbi.nlm.nih.gov/pubmed/26000546 http://dx.doi.org/10.1210/jc.2015-1845 |
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