ADGRL3 (LPHN3) variants predict substance use disorder

ABSTRACT: Genetic factors are strongly implicated in the susceptibility to develop externalizing syndromes such as attentiondeficit/hyperactivity disorder (ADHD), oppositional defiant disorder, conduct disorder, and substance use disorder (SUD). Variants in the ADGRL3 (LPHN3) gene predispose to ADHD...

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Autores:
Arcos Burgos, Oscar Mauricio
Vélez, Jorge I.
Martínez, Ariel F.
Ribasés, Marta
Ramos Quiroga, Josep A.
Sánchez Mora, Cristina
Richarte, Vanesa
Roncero, Carlos
Cormand, Bru
Fernández Castillo, Noelia
Casas, Miguel
Lopera Restrepo, Francisco Javier
Pineda Salazar, David Antonio
Palacio Ortiz, Juan David
Acosta López, Johan E.
Cervantes Henriquez, Martha
Sánchez Rojas, Manuel G.
Puentes Rozo, Pedro J.
Molina, Brooke S. G
Boden, Margaret T.
Wallis, Deeann
Lidbury, Brett
Newman, Saul
Easteal, Simon
Swanson, James
Patel, Hardip
Volkow, Nora
Acosta, Maria T.
Castellanos, Francisco X.
de Leon, Jose
Mastronardi, Claudio A.
Muenke, Maximilian
Tipo de recurso:
Article of investigation
Fecha de publicación:
2019
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/32753
Acceso en línea:
https://hdl.handle.net/10495/32753
Palabra clave:
Attention Deficit Disorder with Hyperactivity
Trastorno por Déficit de Atención con Hiperactividad
Attention Deficit and Disruptive Behavior Disorders
Déficit de la Atención y Trastornos de Conducta Disruptiva
Substance-Related Disorders
Trastornos Relacionados con Sustancias
Conduct Disorder
Trastorno de la Conducta
Genetics
Genética
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABSTRACT: Genetic factors are strongly implicated in the susceptibility to develop externalizing syndromes such as attentiondeficit/hyperactivity disorder (ADHD), oppositional defiant disorder, conduct disorder, and substance use disorder (SUD). Variants in the ADGRL3 (LPHN3) gene predispose to ADHD and predict ADHD severity, disruptive behaviors comorbidity, long-term outcome, and response to treatment. In this study, we investigated whether variants within. ADGRL3 are associated with SUD, a disorder that is frequently co-morbid with ADHD. Using family-based, case-control, and longitudinal samples from disparate regions of the world (n = 2698), recruited either for clinical, genetic epidemiological or pharmacogenomic studies of ADHD, we assembled recursive-partitioning frameworks (classification tree analyses) with clinical, demographic, and ADGRL3 genetic information to predict SUD susceptibility. Our results indicate that SUD can be efficiently and robustly predicted in ADHD participants. The genetic models used remained highly efficient in predicting SUD in a large sample of individuals with severe SUD from a psychiatric institution that were not ascertained on the basis of ADHD diagnosis, thus identifying ADGRL3 as a risk gene for SUD. Recursive-partitioning analyses revealed that rs4860437 was the predominant predictive variant. This new methodological approach offers novel insights into higher order predictive interactions and offers a unique opportunity for translational application in the clinical assessment of patients at high risk for SUD.