Study Report

Study Information

Basic Info
Reference |
Drury, S. S.,2013 PMID: 23647133
|
Citation |
Drury, S. S., et al. (2013). "The association of a novel haplotype in the dopamine transporter with preschool age posttraumatic stress disorder." J Child Adolesc Psychopharmacol 23(4): 236-243. |
Phenotype |
PTSD diagnosis, PTSD symptoms, PTSD category B symptom score, PTSD category C symptom score, PTSD category D symptom score |
Trauma |
Various |
Study Design |
Cross-sectional study |
Study Type |
Candidate gene association study |
Sample Size |
143 samples |
SNP/Marker Size |
1 SNP,1 Variant |
Predominant Ethnicity |
Black, Caucasian |
Population |
87 Black, 41 White, 15 other |
Gender |
86 males, 57 females |
Age |
2 hapolotypes: mean age=5.39 years, SD=1.21, 1 haplotype: mean age=5.20 years, SD=1.15, 0 haplotype: mean age=5.16 years, SD=1.03 |

Detail Info
Sample Diagnosis |
DSM-IV |
Related Diagnostic Tools |
the Preschool Age Psychiatric Assessment (PAPA). The PAPA interview was performed by trained research assistants who were blind to genotyping information. |
Sample Status |
Exclusion criteria were: 1) Head trauma with Glasgow Coma Scale score <7 in the emergency room. 2) Mental retardation, autistic disorder, blindness, deafness, and coming from foreign language-speaking families. |
Controls Exposed |
NA |
Replication Size |
None |
Result Summary |
The number of haplotypes (0, 1, or 2) defined by the presence of the nine repeat allele of rs28363170 (VNTR in the 3'UTR)and the C allele of rs27072 (SNP in the 3'UTR)was significantly associated with both the diagnosis ofPTSDand total PTSD symptoms. Specifically, children with one or two copies of the haplotype had significantly more PTSD symptoms and were more likely to be diagnosed with PTSD than were children without this haplotype. |
Potential Biomarker |
None |

Genetic result reported by this study

Normal genetic result reported by this study (count: 5)
Marker |
Phenotype |
Related Gene |
Statistical Values |
Author Comments |
Marker's Category |
DAT_3'UTR_VNTR-rs27072, nine repeat-C
|
PTSD category D symptom score |
SLC6A3 |
R2=0.09, f=3.6, P-value<0.08, in white subgroup: r2=0.15, P-value<0.04, in black subgroup: r2=0.07, P-value<0.06. |
Haplotype was also significantly associated with Criterion D......
Haplotype was also significantly associated with Criterion D. Haplotype was significantly associated with the number of criterion D symptoms within the white subgroup and approached significance within the black subgroup.
More...
|
Significant |
DAT_3'UTR_VNTR-rs27072, nine repeat-C
|
PTSD category C symptom score |
SLC6A3 |
R2=0.07, f=2.56, P-value<0.05 |
Haplotype was also significantly associated with Criterion C......
Haplotype was also significantly associated with Criterion C.
More...
|
Significant |
DAT_3'UTR_VNTR-rs27072, nine repeat-C
|
PTSD symptoms |
SLC6A3 |
R2=0.1, f=3.81, P-value<0.06, in white subgroup: r2=0.13, P-value<0.07, in black subgroup: r2=0.09, P-value<0.01. |
Haplotype was also significantly associated with total PTSD ......
Haplotype was also significantly associated with total PTSD symptoms. PTSD symptoms within the black subgroup and approached significance with the total number of PTSD symptoms within the white subgroup.
More...
|
Significant |
DAT_3'UTR_VNTR-rs27072, nine repeat-C
|
PTSD diagnosis |
SLC6A3 |
X2=10.47, P-value= 0.005 |
Haplotype status significantly predicted PTSD diagnosis.
Haplotype status significantly predicted PTSD diagnosis.
|
Significant |
DAT_3'UTR_VNTR-rs27072, nine repeat-C
|
PTSD category B symptom score |
SLC6A3 |
No detail information |
None
None
|
Non-significant |