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Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Munn-Chernoff, Melissa A; Johnson, Emma C; Chou, Yi-Ling; Coleman, Jonathan R I; Thornton, Laura M; Walters, Raymond K; Yilmaz, Zeynep; Baker, Jessica H; Hübel, Christopher; Gordon, Scott; Medland, Sarah E; Watson, Hunna J; Gaspar, Héléna A; Bryois, Julien; Hinney, Anke; Leppä, Virpi M; Mattheisen, Manuel; Ripke, Stephan; Yao, Shuyang; Giusti-Rodríguez, Paola; Hanscombe, Ken B; Adan, Roger A H; Alfredsson, Lars; Ando, Tetsuya; Andreassen, Ole A; Berrettini, Wade H; Boehm, Ilka; Boni, Claudette; Boraska Perica, Vesna; Buehren, Katharina; Burghardt, Roland; Cassina, Matteo; Cichon, Sven; Clementi, Maurizio; Cone, Roger D; Courtet, Philippe; Crow, Scott; Crowley, James J; Danner, Unna N; Davis, Oliver S P; de Zwaan, Martina; Dedoussis, George; Degortes, Daniela; DeSocio, Janiece E; Dick, Danielle M; Dikeos, Dimitris; Dina, Christian; Dmitrzak-Weglarz, Monika; Docampo, Elisa; Duncan, Laramie E.
Afiliação
  • Munn-Chernoff MA; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Johnson EC; Department of Psychiatry, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Chou YL; Department of Psychiatry, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Coleman JRI; Social, Genetic and Developmental Psychiatry (SGDP) Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Thornton LM; National Institute for Health Research Biomedical Research Centre, King's College London and South London and Maudsley National Health Service Trust, London, UK.
  • Walters RK; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Yilmaz Z; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Baker JH; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Hübel C; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Gordon S; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Medland SE; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Watson HJ; Social, Genetic and Developmental Psychiatry (SGDP) Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Gaspar HA; National Institute for Health Research Biomedical Research Centre, King's College London and South London and Maudsley National Health Service Trust, London, UK.
  • Bryois J; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Hinney A; QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Leppä VM; QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Mattheisen M; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Ripke S; School of Psychology, Curtin University, Perth, Western Australia, Australia.
  • Yao S; School of Paediatrics and Child Health, University of Western Australia, Perth, Western Australia, Australia.
  • Giusti-Rodríguez P; Social, Genetic and Developmental Psychiatry (SGDP) Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Hanscombe KB; National Institute for Health Research Biomedical Research Centre, King's College London and South London and Maudsley National Health Service Trust, London, UK.
  • Adan RAH; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Alfredsson L; Department of Child and Adolescent Psychiatry, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Ando T; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Andreassen OA; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Berrettini WH; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Boehm I; Center for Psychiatry Research, Stockholm Health Care Services, Stockholm County Council, Stockholm, Sweden.
  • Boni C; Department of Psychiatry, Psychosomatics and Psychotherapy, University of Würzburg, Germany.
  • Boraska Perica V; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Buehren K; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Burghardt R; Department of Psychiatry and Psychotherapy, Charité - Universitätsmedizin, Berlin, Germany.
  • Cassina M; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Cichon S; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Clementi M; Department of Medical and Molecular Genetics, King's College London, Guy's Hospital, London, UK.
  • Cone RD; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Courtet P; Center for Eating Disorders Rintveld, Altrecht Mental Health Institute, Zeist, The Netherlands.
  • Crow S; Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Crowley JJ; Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Danner UN; Department of Behavioral Medicine, National Institute of Mental Health, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.
  • Davis OSP; NORMENT Centre, Division of Mental Health and Addiction, NORMENT Centre, University of Oslo, Oslo University Hospital, Oslo, Norway.
  • de Zwaan M; Department of Psychiatry, Center for Neurobiology and Behavior, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Dedoussis G; Division of Psychological and Social Medicine and Developmental Neurosciences, Faculty of Medicine, Technische Universität Dresden, Dresden, Germany.
  • Degortes D; Centre of Psychiatry and Neuroscience, INSERM U894, Paris, France.
  • DeSocio JE; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • Dick DM; Department of Medical Biology, School of Medicine, University of Split, Split, Croatia.
  • Dikeos D; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, RWTH Aachen University, Aachen, Germany.
  • Dina C; Klinikum Frankfurt/Oder, Frankfurt, Germany.
  • Dmitrzak-Weglarz M; Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, Italy.
  • Docampo E; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
  • Duncan LE; Department of Biomedicine, University of Basel, Basel, Switzerland.
Addict Biol ; 26(1): e12880, 2021 01.
Article em En | MEDLINE | ID: mdl-32064741
ABSTRACT
Eating disorders and substance use disorders frequently co-occur. Twin studies reveal shared genetic variance between liabilities to eating disorders and substance use, with the strongest associations between symptoms of bulimia nervosa and problem alcohol use (genetic correlation [rg ], twin-based = 0.23-0.53). We estimated the genetic correlation between eating disorder and substance use and disorder phenotypes using data from genome-wide association studies (GWAS). Four eating disorder phenotypes (anorexia nervosa [AN], AN with binge eating, AN without binge eating, and a bulimia nervosa factor score), and eight substance-use-related phenotypes (drinks per week, alcohol use disorder [AUD], smoking initiation, current smoking, cigarettes per day, nicotine dependence, cannabis initiation, and cannabis use disorder) from eight studies were included. Significant genetic correlations were adjusted for variants associated with major depressive disorder and schizophrenia. Total study sample sizes per phenotype ranged from ~2400 to ~537 000 individuals. We used linkage disequilibrium score regression to calculate single nucleotide polymorphism-based genetic correlations between eating disorder- and substance-use-related phenotypes. Significant positive genetic associations emerged between AUD and AN (rg = 0.18; false discovery rate q = 0.0006), cannabis initiation and AN (rg = 0.23; q < 0.0001), and cannabis initiation and AN with binge eating (rg = 0.27; q = 0.0016). Conversely, significant negative genetic correlations were observed between three nondiagnostic smoking phenotypes (smoking initiation, current smoking, and cigarettes per day) and AN without binge eating (rgs = -0.19 to -0.23; qs < 0.04). The genetic correlation between AUD and AN was no longer significant after co-varying for major depressive disorder loci. The patterns of association between eating disorder- and substance-use-related phenotypes highlights the potentially complex and substance-specific relationships among these behaviors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Alimentação e da Ingestão de Alimentos / Transtornos Relacionados ao Uso de Substâncias Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Addict Biol Assunto da revista: TRANSTORNOS RELACIONADOS COM SUBSTANCIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Alimentação e da Ingestão de Alimentos / Transtornos Relacionados ao Uso de Substâncias Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Addict Biol Assunto da revista: TRANSTORNOS RELACIONADOS COM SUBSTANCIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos