<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hung CL</submitter><funding>Mackay Memorial Hospital</funding><funding>Ministry of Science and Technology</funding><funding>NIAAA NIH HHS</funding><pagination>638-646</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6246566</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>52(6)</volume><pubmed_abstract>&lt;h4>Aims&lt;/h4>Excessive consumption of alcoholic beverages is associated with cardiac remodeling and cardiomyopathy. We examined the possible association of alcohol use, common Asian genetic variants in genes involved in alcohol metabolism, and cardiac structures/functions alterations.&lt;h4>Methods&lt;/h4>A prospective, community-dwelling survey among individuals with available complete echocardiography examined the associations of alcohol use, cardiac structure/functions, and three common alcohol metabolizing genetic variants, including aldehyde dehydrogenase 2 (ALDH2), alcohol dehydrogenase 1B (ADH1B) and cytochrome P450 (CYP) isoform 2E1 (CYP2E1).&lt;h4>Results&lt;/h4>Among 1577 participants (mean age: 53 ± 9, 59.7% female), we observed that in subjects with more frequent weekly ethanol intake show</pubmed_abstract><journal>Alcohol and alcoholism (Oxford, Oxfordshire)</journal><pubmed_title>Genetic Polymorphisms of Alcohol Metabolizing Enzymes and Alcohol Consumption are Associated With Asymptomatic Cardiac Remodeling and Subclinical Systolic Dysfunction in Large Community-Dwelling Asians.</pubmed_title><pmcid>PMC6246566</pmcid><funding_grant_id>NSC-101-2314-B-195-020</funding_grant_id><funding_grant_id>10271</funding_grant_id><funding_grant_id>101-2314-B-195 -020 –MY1</funding_grant_id><funding_grant_id>E-102003</funding_grant_id><funding_grant_id>MOST 103-2314-B-195-006-MY3</funding_grant_id><funding_grant_id>R37 AA011147</funding_grant_id><funding_grant_id>103-2314-B-195-001-MY3</funding_grant_id><funding_grant_id>10220</funding_grant_id><funding_grant_id>10253</funding_grant_id><funding_grant_id>10375</funding_grant_id><funding_grant_id>NSC102-2314-B-002-046-MY3</funding_grant_id><funding_grant_id>NSC103-2314-B-010-005-MY3</funding_grant_id><funding_grant_id>10358</funding_grant_id><funding_grant_id>10248</funding_grant_id><pubmed_authors>Wang SW</pubmed_authors><pubmed_authors>Chang SC</pubmed_authors><pubmed_authors>Hung CL</pubmed_authors><pubmed_authors>Lai YJ</pubmed_authors><pubmed_authors>Wang LY</pubmed_authors><pubmed_authors>Wu YJ</pubmed_authors><pubmed_authors>Lin SJ</pubmed_authors><pubmed_authors>Chen CH</pubmed_authors><pubmed_authors>Chi PC</pubmed_authors><pubmed_authors>MAGNET Study Investigator</pubmed_authors><pubmed_authors>Chang SH</pubmed_authors><pubmed_authors>Yeh HI</pubmed_authors><pubmed_authors>Mochly-Rosen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic Polymorphisms of Alcohol Metabolizing Enzymes and Alcohol Consumption are Associated With Asymptomatic Cardiac Remodeling and Subclinical Systolic Dysfunction in Large Community-Dwelling Asians.</name><description>&lt;h4>Aims&lt;/h4>Excessive consumption of alcoholic beverages is associated with cardiac remodeling and cardiomyopathy. We examined the possible association of alcohol use, common Asian genetic variants in genes involved in alcohol metabolism, and cardiac structures/functions alterations.&lt;h4>Methods&lt;/h4>A prospective, community-dwelling survey among individuals with available complete echocardiography examined the associations of alcohol use, cardiac structure/functions, and three common alcohol metabolizing genetic variants, including aldehyde dehydrogenase 2 (ALDH2), alcohol dehydrogenase 1B (ADH1B) and cytochrome P450 (CYP) isoform 2E1 (CYP2E1).&lt;h4>Results&lt;/h4>Among 1577 participants (mean age: 53 ± 9, 59.7% female), we observed that in subjects with more frequent weekly ethanol intake show</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Nov</publication><modification>2026-05-06T01:43:51.347Z</modification><creation>2019-03-27T00:10:17Z</creation></dates><accession>S-EPMC6246566</accession><cross_references><pubmed>29016726</pubmed><doi>10.1093/alcalc/agx049</doi></cross_references></HashMap>