Increased fMRI activation during response inhibition, and decreased activation during error processing is associated with possession of the 10-repeat allele of the DAT1 gene: a genetic imaging study investigating the role of the DAT1 gene in Attention Deficit Hyperactivity disorder

NeuroImage ◽  
2009 ◽  
Vol 47 ◽  
pp. S161
Author(s):  
W Braet ◽  
KA Johnson ◽  
CT Tobin ◽  
R Acheson ◽  
C McDonnell ◽  
...  
2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Cempaka Thursina ◽  
Dian Kesumapramudya Nurputra ◽  
Indra Sari Kusuma Harahap ◽  
Nur Imma Fatimah Harahap ◽  
Nihayatus Sa’adah ◽  
...  

Attention deficit hyperactivity disorder (ADHD) is one of the most common neurobehavioural in the children. Genetic factor is known one of the factors which contributed in ADHD development. VNTR polymorphism in 3’UTR exon 15 of DAT1 gene and exon 3 of DRD4 gene are reported to be associated in ADHD. In this study we examine the association of ADHD with VNTR polymorphism of DAT1 and DRD4 gene in Indonesian children. Sixty-five ADHD children and 70 normal children (6- 13 years of age), were included in the study, we matched by age and gender. ADHD was diagnosed by DSM-IV. We performed a casecontrol study to found the association between ADHD and VNTR polymorphism of DAT1 and DRD4 genes. The 10-repeat allele of DAT1 and 2-repeat allele of DRD4 were higher in Indonesian children. Although the frequency of these allele was higher, but it was similar both in ADHD and control groups. Neither DAT1 nor DRD4 gene showed showed significant difference in genotype distribution and frequency allele between both groups (p > 0.05). No association between ADHD and VNTR polymorphism of DAT1 and DRD4 genes found in Indonesian children. This data suggest that DAT1 and DRD4 do not contribute to etiology of ADHD in Indonesian children. Further studies are needed to clarify association between VNTR polymorphism of DAT1 and DRD4 genetic with ADHD of Indonesian children in larger sample size and family based study.


2007 ◽  
Vol 151 (3) ◽  
pp. 211-220 ◽  
Author(s):  
Catharina S. van Meel ◽  
Dirk J. Heslenfeld ◽  
Jaap Oosterlaan ◽  
Joseph A. Sergeant

2021 ◽  
pp. 1-9 ◽  
Author(s):  
Isabella Vainieri ◽  
Joanna Martin ◽  
Anna-Sophie Rommel ◽  
Philip Asherson ◽  
Tobias Banaschewski ◽  
...  

Abstract Background A recent genome-wide association study (GWAS) identified 12 independent loci significantly associated with attention-deficit/hyperactivity disorder (ADHD). Polygenic risk scores (PRS), derived from the GWAS, can be used to assess genetic overlap between ADHD and other traits. Using ADHD samples from several international sites, we derived PRS for ADHD from the recent GWAS to test whether genetic variants that contribute to ADHD also influence two cognitive functions that show strong association with ADHD: attention regulation and response inhibition, captured by reaction time variability (RTV) and commission errors (CE). Methods The discovery GWAS included 19 099 ADHD cases and 34 194 control participants. The combined target sample included 845 people with ADHD (age: 8–40 years). RTV and CE were available from reaction time and response inhibition tasks. ADHD PRS were calculated from the GWAS using a leave-one-study-out approach. Regression analyses were run to investigate whether ADHD PRS were associated with CE and RTV. Results across sites were combined via random effect meta-analyses. Results When combining the studies in meta-analyses, results were significant for RTV (R2 = 0.011, β = 0.088, p = 0.02) but not for CE (R2 = 0.011, β = 0.013, p = 0.732). No significant association was found between ADHD PRS and RTV or CE in any sample individually (p > 0.10). Conclusions We detected a significant association between PRS for ADHD and RTV (but not CE) in individuals with ADHD, suggesting that common genetic risk variants for ADHD influence attention regulation.


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