Moderate alcohol use and cardiovascular disease from Mendelian randomization.
Observational studies show moderate alcohol use negatively associated with ischemic heart disease (IHD) and cardiovascular disease (CVD). However, healthier attributes among moderate users compared to never users may confound the apparent association. A potentially less biased way to examine the ass...
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doaj-1e4b8fb0abc04d5eaf106df274bac6322020-11-25T00:44:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6805410.1371/journal.pone.0068054Moderate alcohol use and cardiovascular disease from Mendelian randomization.Shiu Lun Au YeungChaoqiang JiangKar Keung ChengBenjamin J CowlingBin LiuWeisen ZhangTai Hing LamGabriel M LeungC Mary SchoolingObservational studies show moderate alcohol use negatively associated with ischemic heart disease (IHD) and cardiovascular disease (CVD). However, healthier attributes among moderate users compared to never users may confound the apparent association. A potentially less biased way to examine the association is Mendelian randomization, using alcohol metabolizing genes which influence alcohol use.We used instrumental variable analysis with aldehyde dehydrogenase 2 (ALDH2) genotypes (AA/GA/GG) as instrumental variables for alcohol use to examine the association of alcohol use (10 g ethanol/day) with CVD risk factors (blood pressure, lipids and glucose) and morbidity (self-reported IHD and CVD) among men in the Guangzhou Biobank Cohort Study.ALDH2 genotypes were a credible instrument for alcohol use (F-statistic 74.6). Alcohol was positively associated with HDL-cholesterol (0.05 mmol/L per alcohol unit, 95% confidence interval (CI) 0.02 to 0.08) and diastolic blood pressure (1.15 mmHg, 95% CI 0.23 to 2.07) but not with systolic blood pressure (1.00 mmHg, 95% CI -0.74 to 2.74), LDL-cholesterol (0.03 mmol/L, 95% CI -0.03 to 0.08), log transformed triglycerides (0.03 mmol/L, 95% CI -0.01 to 0.08) or log transformed fasting glucose (0.01 mmol/L, 95% CI -0.006 to 0.03), self-reported CVD (odds ratio (OR) 0.98, 95% CI 0.76 to 1.27) or self-reported IHD (OR 1.10, 95% CI 0.83 to 1.45).Low to moderate alcohol use among men had the expected effects on most CVD risk factors but not fasting glucose. Larger studies are needed to confirm the null associations with IHD, CVD and fasting glucose.http://europepmc.org/articles/PMC3712994?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shiu Lun Au Yeung Chaoqiang Jiang Kar Keung Cheng Benjamin J Cowling Bin Liu Weisen Zhang Tai Hing Lam Gabriel M Leung C Mary Schooling |
spellingShingle |
Shiu Lun Au Yeung Chaoqiang Jiang Kar Keung Cheng Benjamin J Cowling Bin Liu Weisen Zhang Tai Hing Lam Gabriel M Leung C Mary Schooling Moderate alcohol use and cardiovascular disease from Mendelian randomization. PLoS ONE |
author_facet |
Shiu Lun Au Yeung Chaoqiang Jiang Kar Keung Cheng Benjamin J Cowling Bin Liu Weisen Zhang Tai Hing Lam Gabriel M Leung C Mary Schooling |
author_sort |
Shiu Lun Au Yeung |
title |
Moderate alcohol use and cardiovascular disease from Mendelian randomization. |
title_short |
Moderate alcohol use and cardiovascular disease from Mendelian randomization. |
title_full |
Moderate alcohol use and cardiovascular disease from Mendelian randomization. |
title_fullStr |
Moderate alcohol use and cardiovascular disease from Mendelian randomization. |
title_full_unstemmed |
Moderate alcohol use and cardiovascular disease from Mendelian randomization. |
title_sort |
moderate alcohol use and cardiovascular disease from mendelian randomization. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
Observational studies show moderate alcohol use negatively associated with ischemic heart disease (IHD) and cardiovascular disease (CVD). However, healthier attributes among moderate users compared to never users may confound the apparent association. A potentially less biased way to examine the association is Mendelian randomization, using alcohol metabolizing genes which influence alcohol use.We used instrumental variable analysis with aldehyde dehydrogenase 2 (ALDH2) genotypes (AA/GA/GG) as instrumental variables for alcohol use to examine the association of alcohol use (10 g ethanol/day) with CVD risk factors (blood pressure, lipids and glucose) and morbidity (self-reported IHD and CVD) among men in the Guangzhou Biobank Cohort Study.ALDH2 genotypes were a credible instrument for alcohol use (F-statistic 74.6). Alcohol was positively associated with HDL-cholesterol (0.05 mmol/L per alcohol unit, 95% confidence interval (CI) 0.02 to 0.08) and diastolic blood pressure (1.15 mmHg, 95% CI 0.23 to 2.07) but not with systolic blood pressure (1.00 mmHg, 95% CI -0.74 to 2.74), LDL-cholesterol (0.03 mmol/L, 95% CI -0.03 to 0.08), log transformed triglycerides (0.03 mmol/L, 95% CI -0.01 to 0.08) or log transformed fasting glucose (0.01 mmol/L, 95% CI -0.006 to 0.03), self-reported CVD (odds ratio (OR) 0.98, 95% CI 0.76 to 1.27) or self-reported IHD (OR 1.10, 95% CI 0.83 to 1.45).Low to moderate alcohol use among men had the expected effects on most CVD risk factors but not fasting glucose. Larger studies are needed to confirm the null associations with IHD, CVD and fasting glucose. |
url |
http://europepmc.org/articles/PMC3712994?pdf=render |
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