Literature DB >> 22531292

Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort.

Emma S Nyman1, Anu Loukola, Teppo Varilo, Anja Taanila, Tuula Hurtig, Irma Moilanen, Sandra Loo, James J McGough, Marjo-Riitta Järvelin, Susan L Smalley, Stanley F Nelson, Leena Peltonen.   

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a childhood-onset neurodevelopmental disorder with a significant public-health impact. Previously, we described a candidate gene study in a population-based birth cohort that demonstrated an association with ADHD-affected males and the dopamine receptor D2 (DRD2). The current study evaluates potential associations of dopamine receptor genes and Cloninger temperament traits within this same sample. Participants with stringent lifetime ADHD diagnoses were ascertained systematically from the genetically isolated Northern Finland 1986 Birth Cohort (n=9432), resulting in 178 cases and 157 controls. Markers in all known dopamine receptor genes were genotyped. We report an association of DRD2 with low Persistence in females (rs1079727 P=0.02, rs1124491 P=0.02, rs1800497 P=0.03). The associated DRD2 minor allelic haplotype (CAA, P=0.03) is the same haplotype we previously associated with ADHD in males in this birth cohort. The current study further supports previous results on the role of DRD2 in individuals with ADHD. Investigations suggest that DRD2 may have an impact on both males and females, but the particular outcome appears sex-specific, manifesting as ADHD in males and low Persistence in females. Furthermore, these findings suggest that the putative role of low Persistence as an endophenotype for ADHD deserves further investigation.

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Year:  2012        PMID: 22531292     DOI: 10.1097/YPG.0b013e32834c0cc8

Source DB:  PubMed          Journal:  Psychiatr Genet        ISSN: 0955-8829            Impact factor:   2.458


  8 in total

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2.  Predicting substance use in emerging adulthood: A genetically informed study of developmental transactions between impulsivity and family conflict.

Authors:  Kit K Elam; Frances L Wang; Kaitlin Bountress; Laurie Chassin; Danielle Pandika; Kathryn Lemery-Chalfant
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4.  Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins.

Authors:  Fang-Fen Yuan; Xue Gu; Xin Huang; Yu-Wei Hou; Yan Zhong; Jun Lin; Jing Wu
Journal:  PLoS One       Date:  2017-11-27       Impact factor: 3.240

5.  Temperament Traits Mark Liability for Coexisting Psychiatric Symptoms in Children With Elevated ADHD Symptoms.

Authors:  Tara M Rutter; Anne B Arnett
Journal:  J Atten Disord       Date:  2020-07-22       Impact factor: 3.256

6.  Genetic variation in the human brain dopamine system influences motor learning and its modulation by L-Dopa.

Authors:  Kristin M Pearson-Fuhrhop; Brian Minton; Daniel Acevedo; Babak Shahbaba; Steven C Cramer
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7.  The Molecular Neurobiology of Twelve Steps Program & Fellowship: Connecting the Dots for Recovery.

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Journal:  J Reward Defic Syndr       Date:  2015

8.  Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population.

Authors:  Huan Chen; Guoqing Wang; Jiguang Xia; Yuxi Zhou; Yong Gao; Junquan Xu; Michael Sy Huen; Wai Ting Siok; Yuyang Jiang; Li Hai Tan; Yimin Sun
Journal:  Behav Brain Funct       Date:  2014-09-01       Impact factor: 3.759

  8 in total

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