{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,25]],"date-time":"2026-03-25T20:44:28Z","timestamp":1774471468334,"version":"3.50.1"},"reference-count":44,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["Circ: Genomic and Precision Medicine"],"published-print":{"date-parts":[[2025,4]]},"abstract":"<jats:sec>\n            <jats:title>BACKGROUND:<\/jats:title>\n            <jats:p>Whether prolonged and excessive alcohol consumption contributes to dilated cardiomyopathy (DCM) remains uncertain. This study aimed to describe the prevalence of alcohol use in patients with DCM and their first-degree relatives (FDRs) and determine if cumulative alcohol exposure associates with DCM\/partial DCM or modifies the association of DCM with DCM-relevant rare variants.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>METHODS:<\/jats:title>\n            <jats:p>All probands had DCM; FDRs were classified as with or without DCM or partial DCM. Alcohol exposure was measured with the Alcohol Use Disorder Identification Test-Consumption questionnaire and years of drinking. Rare variants in 36 DCM genes were classified as pathogenic, likely pathogenic, or variants of uncertain significance (pathogenic, likely pathogenic, variant of uncertain significance). Generalized linear mixed models were used to assess the association of DCM\/partial DCM with alcohol use among FDRs.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>RESULTS:<\/jats:title>\n            <jats:p>\n              DCM\/partial DCM was found in 21.8% of 1373 FDRs of 1148 DCM probands. The prevalence of former or current alcohol use was 68% for probands and 70% for FDRs. About 30% of probands and 37% of FDRs had positive Alcohol Use Disorder Identification Test-Consumption scores, indicating moderate or heavy drinking. Among FDRs, DCM\/partial DCM was associated with the presence of pathogenic\/likely pathogenic variants in DCM genes (odds ratio, 3.51 [95% CI, 2.33\u20135.29]) but not with alcohol exposure. Cumulative alcohol exposure was not found to modify the association between DCM\/partial DCM and these variants (\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.55).\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>CONCLUSIONS:<\/jats:title>\n            <jats:p>Alcohol use was frequent among probands and FDRs. This study did not provide evidence supporting an association of cumulative alcohol exposure with DCM\/partial DCM or a modifying effect of alcohol use on the association of DCM with DCM-relevant rare variants.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>REGISTRATION:<\/jats:title>\n            <jats:p>\n              URL:\n              <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/www.clinicaltrials.gov\">https:\/\/www.clinicaltrials.gov<\/jats:ext-link>\n              ; Unique identifier: NCT03037632.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/circgen.124.004946","type":"journal-article","created":{"date-parts":[[2025,3,28]],"date-time":"2025-03-28T09:01:23Z","timestamp":1743152483000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Alcohol Exposure Among Patients With Dilated Cardiomyopathy and Their First-Degree Relatives: The DCM Precision Medicine Study"],"prefix":"10.1161","volume":"18","clinical-trial-number":[{"clinical-trial-number":"nct03037632","registry":"10.18810\/clinical-trials-gov"}],"author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8788-9479","authenticated-orcid":true,"given":"Javier","family":"Jimenez","sequence":"first","affiliation":[{"name":"Miami Cardiac and Vascular Institute, FL (J.J., S.C.)."},{"name":"Herbert Wertheim College of Medicine, Florida International University, Miami (J.J., M.R., S.C., A.S.)."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0175-5718","authenticated-orcid":true,"given":"Hanyu","family":"Ni","sequence":"additional","affiliation":[{"name":"The Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus (H.N., J.C., J.O.M., N.H., P.K.P., E.J., D.D.K., R.E.H.)."},{"name":"The Davis Heart and Lung Research Institute, The Ohio State University, Columbus (H.N., G.J.H., J.C., J.O.M., N.H., P.K.P., E.J., D.D.K., R.E.H.)."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2340-2021","authenticated-orcid":true,"given":"Stuart D.","family":"Katz","sequence":"additional","affiliation":[{"name":"NYU Langone Health, Leon H. 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