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Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response

BACKGROUND: This study examined the relationship between alcohol consumption and hyperhomocysteinemia based on facial flushing caused by drinking. METHODS: Among male patients aged ≥ 18 years who visited Health Promotion Center of Chungnam National University Hospital in Daejeon from January 2008 to...

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Autores principales: Kim, Eo-Chin, Kim, Jong Sung, Jung, Jin-Gyu, Kim, Sung-Soo, Yoon, Seok-Joon, Ryu, Jung-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Family Medicine 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726792/
https://www.ncbi.nlm.nih.gov/pubmed/23904954
http://dx.doi.org/10.4082/kjfm.2013.34.4.250
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author Kim, Eo-Chin
Kim, Jong Sung
Jung, Jin-Gyu
Kim, Sung-Soo
Yoon, Seok-Joon
Ryu, Jung-Sun
author_facet Kim, Eo-Chin
Kim, Jong Sung
Jung, Jin-Gyu
Kim, Sung-Soo
Yoon, Seok-Joon
Ryu, Jung-Sun
author_sort Kim, Eo-Chin
collection PubMed
description BACKGROUND: This study examined the relationship between alcohol consumption and hyperhomocysteinemia based on facial flushing caused by drinking. METHODS: Among male patients aged ≥ 18 years who visited Health Promotion Center of Chungnam National University Hospital in Daejeon from January 2008 to December 2010, 948 males (182 nondrinkers, 348 subjects with drinking-related facial flushing, and 418 subjects without drinking-related facial flushing) were selected. After adjusting for confounding factors such as age, body mass index, hypertension, diabetes, smoking, triglycerides, high density lipoprotein cholesterol, and gamma-glutamyl transpeptidase, a multiple logistic regression analysis was performed to assess the risk of hyperhomocysteinemia in the nonfacial flushing and facial flushing groups compared with the nondrinkers. RESULTS: After adjusting for confounding factors, risk of hyperhomocysteinemia was significantly lower in the group with a weekly alcohol consumption of < 8 standard drinks (1 drink = 14 g alcohol) in the nonfacial flushing group (<4 drinks: odds ratio [OR], 0.27; 95% confidence interval [CI], 0.10 to 0.74; 4≤, <8 drinks: OR, 0.21; 95% CI, 0.06 to 0.73). Risk of hyperhomocysteinemia was significantly lower in the group with a weekly alcohol consumption < 4 drinks in the facial flushing group (OR, 0.30; 95% CI, 0.13 to 0.68). CONCLUSION: Our results suggest that the risk of hyperhomocysteinemia is likely lowered by alcohol consumption based on drinking quantity, as lowering the risk of hyperhomocysteinemia differs depending on vulnerability associated with facial flushing.
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spelling pubmed-37267922013-07-31 Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response Kim, Eo-Chin Kim, Jong Sung Jung, Jin-Gyu Kim, Sung-Soo Yoon, Seok-Joon Ryu, Jung-Sun Korean J Fam Med Original Article BACKGROUND: This study examined the relationship between alcohol consumption and hyperhomocysteinemia based on facial flushing caused by drinking. METHODS: Among male patients aged ≥ 18 years who visited Health Promotion Center of Chungnam National University Hospital in Daejeon from January 2008 to December 2010, 948 males (182 nondrinkers, 348 subjects with drinking-related facial flushing, and 418 subjects without drinking-related facial flushing) were selected. After adjusting for confounding factors such as age, body mass index, hypertension, diabetes, smoking, triglycerides, high density lipoprotein cholesterol, and gamma-glutamyl transpeptidase, a multiple logistic regression analysis was performed to assess the risk of hyperhomocysteinemia in the nonfacial flushing and facial flushing groups compared with the nondrinkers. RESULTS: After adjusting for confounding factors, risk of hyperhomocysteinemia was significantly lower in the group with a weekly alcohol consumption of < 8 standard drinks (1 drink = 14 g alcohol) in the nonfacial flushing group (<4 drinks: odds ratio [OR], 0.27; 95% confidence interval [CI], 0.10 to 0.74; 4≤, <8 drinks: OR, 0.21; 95% CI, 0.06 to 0.73). Risk of hyperhomocysteinemia was significantly lower in the group with a weekly alcohol consumption < 4 drinks in the facial flushing group (OR, 0.30; 95% CI, 0.13 to 0.68). CONCLUSION: Our results suggest that the risk of hyperhomocysteinemia is likely lowered by alcohol consumption based on drinking quantity, as lowering the risk of hyperhomocysteinemia differs depending on vulnerability associated with facial flushing. The Korean Academy of Family Medicine 2013-07 2013-07-24 /pmc/articles/PMC3726792/ /pubmed/23904954 http://dx.doi.org/10.4082/kjfm.2013.34.4.250 Text en Copyright © 2013 The Korean Academy of Family Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Eo-Chin
Kim, Jong Sung
Jung, Jin-Gyu
Kim, Sung-Soo
Yoon, Seok-Joon
Ryu, Jung-Sun
Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response
title Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response
title_full Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response
title_fullStr Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response
title_full_unstemmed Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response
title_short Effect of Alcohol Consumption on Risk of Hyperhomocysteinemia Based on Alcohol-Related Facial Flushing Response
title_sort effect of alcohol consumption on risk of hyperhomocysteinemia based on alcohol-related facial flushing response
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726792/
https://www.ncbi.nlm.nih.gov/pubmed/23904954
http://dx.doi.org/10.4082/kjfm.2013.34.4.250
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