4.1 Article

Dopamine Transporter Gene Polymorphism Moderates the Effects of Severe Deprivation on ADHD Symptoms: Developmental Continuities in Gene-Environment Interplay

出版社

WILEY
DOI: 10.1002/ajmg.b.31010

关键词

gene-environment interaction; DAT1 gene; longitudinal study; attention-deficit/hyperactivity disorder

资金

  1. Economic and Social Research Council (ESRC)
  2. UCB Pharma [PTA-033-2004-00014]
  3. Helmut Horten Foundation
  4. UK Department of Health
  5. Department of Health
  6. Nuffield Foundation
  7. Jacobs Foundation
  8. Economic and Social Research Council
  9. UCB Pharma Ltd
  10. Janssen-Cilag
  11. German Academy of Sciences Leopoldina [BMBF-LPD 99081/8168]
  12. Janssen Cilag
  13. Flynn Pharma

向作者/读者索取更多资源

Early institutional deprivation is a risk factor for Attention-Deficit/Hyperactivity Disorder (ADHD) symptoms. However not all individuals are affected. We tested the hypothesis that this heterogeneity is influenced by gene x environment (GxE) interaction and that genetic polymorphisms involved in dopamine neurotransmission moderate the effects of severe early institutional deprivation on symptoms of ADHD (sADHD). Using a prospective-longitudinal design sADHD were measured at ages 6, 11, and 15 years in a sample of individuals who experienced severe institutional deprivation (up to 42 months of age) in Romanian orphanages and a non-institutionalized comparison group. Individuals were genotyped for polymorphisms in the dopamine D4 receptor (DRD448-bp VNTR in exon 3) and dopamine transporter gene (DAT1 haplotypes combining a 40-bp VNTR in 3'UTR and a 30-bp VNTR in intron 8). The risk for sADHD associated with early institutional deprivation was moderated by the DAT1 but not the DRD4 genotypes; an effect that was first apparent in early-, and persisted to mid-adolescence. The results (i) provide evidence for developmental continuities in G x E interaction, (ii) explain some of the heterogeneity in ADHD outcomes following institutional deprivation and, (iii) add to our understanding of environmental determinants of sADHD. (C) 2009 Wiley-Liss, Inc.

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