Study Report

Study Information

Basic Info
Reference |
Kolassa, I. T.,2010 PMID: 19944409
|
Citation |
Kolassa, I. T., et al. (2010). "The risk of posttraumatic stress disorder after trauma depends on traumatic load and the catechol-o-methyltransferase Val(158)Met polymorphism." Biol Psychiatry 67(4): 304-308. |
Phenotype |
Lifetime PTSD, Probability of developing lifetime PTSD, Probability of suffering from lifetime PTSD |
Trauma |
1994 Rwandan civil war |
Study Design |
Case-control |
Study Type |
Candidate gene association study, Gene-environment interaction study |
Sample Size |
424 survivors |
SNP/Marker Size |
1 SNP |
Predominant Ethnicity |
Black |
Population |
Uganda |
Gender |
226 male, 198 female |
Age |
Mean age=34.8 years, SD=5.8, age range 17-68. |

Detail Info
Sample Diagnosis |
DSM-IV |
Related Diagnostic Tools |
Posttraumatic Diagnostic Scale (PDS), Depressive symptoms were assessed with the depression section of the Hopkins Symptom Checklist (HSCL-D). Traumatic events were assessed with a checklist of 36 war- and non-war-related traumatic event types (e.g., injury by weapon, rape, accident). Traumatic load was estimated by assessing the number of different traumatic event types experienced or witnessed. |
Sample Status |
Four hundred twenty-four Rwandese refugees from the 1994 Rwandan civil war who were living in the Nakivale refugee camp in southwestern Uganda were investigated. |
Controls Exposed |
Yes |
Replication Size |
None |
Result Summary |
Higher numbers of different lifetime traumatic event types led to a higher prevalence of lifetime PTSD in a dose-response relationship. However, this effect was modulated by the COMT genotype: whereas Val allele carriers showed the typical dose-response relationship, Met/Met homozygotes exhibited a high risk for PTSD independently of the severity of traumatic load. The present findings indicate a gene-environment interaction between the human COMT Val158Met polymorphism and the number of traumatic event types experienced in the risk of developing PTSD. |
Potential Biomarker |
None |

Genetic result reported by this study