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Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans
Previous studies have indicated an association of higher alcohol intake with cardiovascular disease and related traits, but causation has not been definitively established. In this study, the causal effect of alcohol intake on hypertension in 2,011 men and women from the Ansan-Ansung cohort was esti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765011/ https://www.ncbi.nlm.nih.gov/pubmed/29323248 http://dx.doi.org/10.1038/s41598-017-18856-z |
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author | Cho, Yoonsu Kwak, Soyoung Lewis, Sarah J. Wade, Kaitlin H. Relton, Caroline L. Smith, George Davey Shin, Min-Jeong |
author_facet | Cho, Yoonsu Kwak, Soyoung Lewis, Sarah J. Wade, Kaitlin H. Relton, Caroline L. Smith, George Davey Shin, Min-Jeong |
author_sort | Cho, Yoonsu |
collection | PubMed |
description | Previous studies have indicated an association of higher alcohol intake with cardiovascular disease and related traits, but causation has not been definitively established. In this study, the causal effect of alcohol intake on hypertension in 2,011 men and women from the Ansan-Ansung cohort was estimated using an instrumental variable (IV) approach, with both a phenotypic and genotypic instrument for alcohol intake: alcohol flushing and the rs671 genotype (in the alcohol dehydrogenase 2 [ALDH2] gene), respectively. Both alcohol flushing and the rs671 genotype were associated with alcohol intake (difference in alcohol intake with alcohol flushers vs. non-flushers: −9.07 g/day; 95% confidence interval [CI]: −11.12, −7.02; P-value: 8.3 × 10(−18) and with the rs671 GA + AA vs. GG genotype: −7.94 g/day; 95% CI: −10.20, −5.69; P-value: 6.1 × 10(−12)). An increase in alcohol intake, as predicted by both the absence of alcohol flushing and the presence of the rs671 GG genotype in the IV analyses, was associated with an increase in blood pressure in men from this Korean population. In conclusion, this study supports a causal effect of alcohol intake on hypertension and indicated that alcohol flushing may be a valid proxy for the ALDH2 rs671 polymorphism, which influences alcohol intake in this Korean population. |
format | Online Article Text |
id | pubmed-5765011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57650112018-01-17 Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans Cho, Yoonsu Kwak, Soyoung Lewis, Sarah J. Wade, Kaitlin H. Relton, Caroline L. Smith, George Davey Shin, Min-Jeong Sci Rep Article Previous studies have indicated an association of higher alcohol intake with cardiovascular disease and related traits, but causation has not been definitively established. In this study, the causal effect of alcohol intake on hypertension in 2,011 men and women from the Ansan-Ansung cohort was estimated using an instrumental variable (IV) approach, with both a phenotypic and genotypic instrument for alcohol intake: alcohol flushing and the rs671 genotype (in the alcohol dehydrogenase 2 [ALDH2] gene), respectively. Both alcohol flushing and the rs671 genotype were associated with alcohol intake (difference in alcohol intake with alcohol flushers vs. non-flushers: −9.07 g/day; 95% confidence interval [CI]: −11.12, −7.02; P-value: 8.3 × 10(−18) and with the rs671 GA + AA vs. GG genotype: −7.94 g/day; 95% CI: −10.20, −5.69; P-value: 6.1 × 10(−12)). An increase in alcohol intake, as predicted by both the absence of alcohol flushing and the presence of the rs671 GG genotype in the IV analyses, was associated with an increase in blood pressure in men from this Korean population. In conclusion, this study supports a causal effect of alcohol intake on hypertension and indicated that alcohol flushing may be a valid proxy for the ALDH2 rs671 polymorphism, which influences alcohol intake in this Korean population. Nature Publishing Group UK 2018-01-11 /pmc/articles/PMC5765011/ /pubmed/29323248 http://dx.doi.org/10.1038/s41598-017-18856-z Text en © The Author(s) 2017 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 Cho, Yoonsu Kwak, Soyoung Lewis, Sarah J. Wade, Kaitlin H. Relton, Caroline L. Smith, George Davey Shin, Min-Jeong Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans |
title | Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans |
title_full | Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans |
title_fullStr | Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans |
title_full_unstemmed | Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans |
title_short | Exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in Koreans |
title_sort | exploring the utility of alcohol flushing as an instrumental variable for alcohol intake in koreans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765011/ https://www.ncbi.nlm.nih.gov/pubmed/29323248 http://dx.doi.org/10.1038/s41598-017-18856-z |
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