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Shared Genetic Factors Influence Risk for Bipolar Disorder and Alcoholism

dc.creatorPeralta Fernández, Juan Manuel
dc.creatorAlmasy, Laura
dc.creatorContreras Rojas, Javier
dc.creatorPacheco Arce, Adriana
dc.creatorEscamilla, Michael A.
dc.creatorRaventós Vorst, Henriette
dc.creatorGlahn, David C.
dc.creatorCarmiol Del Valle, Nasdia
dc.date.accessioned2019-03-04T20:54:20Z
dc.date.available2019-03-04T20:54:20Z
dc.date.issued2014-06
dc.description.abstractBipolar disorder and alcoholism have high rate comorbidity, with more than 50% of alcoholism occurrence in bipolar disorder. While there is evidence that both disorders are heritable, it is unclear if the same genetic factors predispose them. The aim of this study is to determine if common genetic factors influence risk for bipolar disorder and alcoholism. A total of 733 Costa Rican individuals from 61 extended pedigrees, selected for sibling pairs with a diagnosis of bipolar disorder, participated in the study. All subjects completed a diagnostic interview, the Barratt Impulsiveness Scale (BIS-11) and Fagerström questionnaire for Nicotine Dependence. Heritability and bivariate correlations were estimated using SOLAR. Based on a best-estimate process, twenty-nine percent of the sample met criteria for broad bipolar phenotype, 23% bipolar I disorder, 15% alcoholism, 32% smoking, only 2% drug abuse, and 20% for an anxiety disorder. Thirty-three present did not meet criteria for a lifetime diagnosis. In the broad bipolar phenotype group, 28% had a lifetime diagnosis of alcoholism. The heritability estimated for broad bipolar phenotype was h2=0.559 (p=7.0x10-6) and for alcoholism was h2=0.752 (p=3.0x10-7). Only alcoholism (ρg=0.600, p=0.002) and habitual smoking (ρg=0.717, p=2.1x10-4) were significantly genetically correlated with the broad bipolar phenotype. A similar pattern of results was observed for the bipolar I disorder phenotype. The current findings strongly imply that shared genetic factors increase risk for bipolar disorder and addictive disorders. A better understanding of this comorbidity could improve clinical outcomes and potentially facilitate novel treatments.es
dc.description.procedenceUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Biología Celular y Molecular (CIBCM)es
dc.description.procedenceUCR::Vicerrectoría de Docencia::Ciencias Básicas::Facultad de Ciencias::Escuela de Biologíaes
dc.description.sponsorshipNational Institutes of Health/[MH080912]/NIH/Estados Unidoses
dc.description.sponsorshipNational Institutes of Health/[MH059490]/NIH/Estados Unidoses
dc.identifier.citationhttps://www.europsy-journal.com/article/S0924-9338(13)00424-0/fulltext
dc.identifier.doihttps://doi.org/10.1016/j.eurpsy.2013.10.001
dc.identifier.issn0924-9338
dc.identifier.urihttps://hdl.handle.net/10669/76647
dc.language.isoen_US
dc.rightsacceso embargado
dc.rightsacceso abierto
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceEuropean Psychiatry, vol. 29(5), pp. 282–287es
dc.subjectBipolar disorderes
dc.subjectAlcohol use disorderes
dc.subjectFamily studieses
dc.subjectHeritabilityes
dc.subjectGenetic correlationes
dc.subjectCentral Valley of Costa Ricaes
dc.subject616.895 Psicosis maníacodepresiva (Trastornos bipolares)es
dc.titleShared Genetic Factors Influence Risk for Bipolar Disorder and Alcoholismes
dc.typeartículo original

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