Dopamine transporter (DAT1) gene in combat veterans with PTSD: A case-control study

被引:8
作者
Zuschlag, Zachary D. [1 ,2 ]
Compean, Ebele [3 ]
Nietert, Paul [4 ]
Lauzon, Steven [4 ]
Hamner, Mark [3 ,5 ]
Wang, Zhewu [3 ,5 ]
机构
[1] James A Haley Vet Hosp, Mental Hlth & Behav Sci Serv, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Psychiat & Behav Neurosci, Tampa, FL 33620 USA
[3] Med Univ South Carolina, Dept Psychiat & Behav Sci, 109 Bee St, Charleston, SC 29401 USA
[4] Med Univ South Carolina, Dept Publ Hlth Sci, Charleston, SC 29401 USA
[5] Ralph H Johnson Vet Affairs Med Ctr, Mental Hlth Serv, Charleston, SC USA
关键词
PTSD; Genetics; Veterans; DAT1; CAPS; Combat; Trauma; POSTTRAUMATIC-STRESS-DISORDER; SEROTONIN TRANSPORTER; RACIAL-DIFFERENCES; VIETNAM VETERANS; BETA-HYDROXYLASE; PLASMA DOPAMINE; VNTR; AVAILABILITY; ASSOCIATION; SYMPTOMS;
D O I
10.1016/j.psychres.2021.113801
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The dopamine transporter (DAT1) gene has been postulated to be involved in PTSD; however, existing studies have shown inconsistencies when examining genotypic and allelic associations. The primary objective of this study was to examine whether DAT1?40bp-VNTR (DAT1) 9R polymorphism might increase the risk of PTSD development in combat veterans, utilizing a case-control gene association study with both control and PTSD cases having previous exposure to combat traumas. Participants with PTSD (N = 365) and combat-exposed controls without PTSD (N = 298) were included in analysis. After controlling for race, sex and age, when dichotomized, absence of DAT1 10R/10R genotypes was associated with PTSD diagnosis compared to no PTSD diagnosis; these results were not statistically significant when trichotomized 10R/10R, 10R/X, 9R/9R. Similarly, odds ratio for absence of 10R/10R genotype showed a statistically significant increase in the risk of developing PTSD. DAT1 genotype was also associated with statistically significant mean total CAPS scores, both when dichotomized and trichotomized. In conclusion, our results indicate that the absence of 10R/10R is associated with an increased risk of PTSD and higher CAPS total scores.
引用
收藏
页数:6
相关论文
共 41 条
[1]  
Abdolmaleky Hamid Mostafavi, 2008, V448, P187, DOI 10.1007/978-1-59745-205-2_9
[2]  
Adler L A, 2004, J Atten Disord, V8, P11, DOI 10.1177/108705470400800102
[3]   Atomoxetine treatment may decrease striatal dopaminergic transporter availability after 8 weeks: pilot SPECT report of three cases [J].
Akay, Aynur Pekcanlar ;
Kaya, Gamze Capa ;
Baykara, Burak ;
Demir, Yusuf ;
Ozek, Handan ;
Alsen, Sevay ;
Eren, Mine Sencan ;
Emiroglu, Neslihan Inal ;
Ertay, Turkan ;
Ozturk, Yesim ;
Miral, Suha ;
Durak, Hatice ;
Tufan, Evren .
NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2015, 11 :2909-2911
[4]  
[Anonymous], 2007, STRUCTURED CLIN INTE
[5]   PTSD and dopaminergic genes, DRD2 and DAT, in multigenerational families exposed to the Spitak earthquake [J].
Bailey, Julia N. ;
Goenjian, Armen K. ;
Noble, Ernest P. ;
Walling, David P. ;
Ritchie, Terry ;
Goenjian, Haig A. .
PSYCHIATRY RESEARCH, 2010, 178 (03) :507-510
[6]   The genetic background to PTSD [J].
Broekman, B. F. P. ;
Olff, M. ;
Boer, F. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2007, 31 (03) :348-362
[7]   Molecular Variation at the SLC6A3 Locus Predicts Lifetime Risk of PTSD in the Detroit Neighborhood Health Study [J].
Chang, Shun-Chiao ;
Koenen, Karestan C. ;
Galea, Sandro ;
Aiello, Allison E. ;
Soliven, Richelo ;
Wildman, Derek E. ;
Uddin, Monica .
PLOS ONE, 2012, 7 (06)
[8]   DNA Methylation at the DAT Promoter and Risk for Psychopathology: Intergenerational Transmission between School-Age Youths and Their Parents in a Community Sample [J].
Cimino, Silvia ;
Cerniglia, Luca ;
Ballarotto, Giulia ;
Marzilli, Eleonora ;
Pascale, Esterina ;
D'Addario, Claudio ;
Adriani, Walter ;
Tambelli, Renata .
FRONTIERS IN PSYCHIATRY, 2018, 8
[9]  
Courois C., 2017, CLIN PRACTICE GUIDEL
[10]   Comorbidity/Overlapping Between ADHD and PTSD in Relation to IQ Among Children of Traumatized/Non-Traumatized Parents [J].
Daud, Atia ;
Rydelius, Per-Anders .
JOURNAL OF ATTENTION DISORDERS, 2009, 13 (02) :188-196