Associations between Polymorphisms in the Solute Carrier Family 6 Member 3 and the Myelin Basic Protein Gene and Posttraumatic Stress Disorder.

基因 临床心理学 生物 单倍型 遗传学 遗传关联 全基因组关联研究 内科学 创伤后应激 候选基因 心理学
作者
Muminovic Umihanic M,Romana Babić,N. Kravić,Esmina Avdibegović,Dzubur Kulenovic A,Ferid Agani,Miro Jakovljević,Dragan Babić,Abdulah Kucukalic,Sabina Kucukalic,Sabic Dzananovic E,Bravo Mehmedbasic A,Goci Uka A,Shpend Haxhibeqiri,Blerina Hoxha,Haxhibeqiri,Aukst Margetic B,Nenad Jakšić,Cima Franc A,Dusko Rudan,Marko Pavlović,Feric Bojic E,Damir Marjanović,Nada Bozina,Christiane Ziegler,Christiane Wolf,Bodo Warrings,Katharina Domschke,Juergen Deckert,Osman Sinanović
出处
期刊:Psychiatria Danubina [Medicinska Naklada d.o.o.]
卷期号:31 (2): 235-240 被引量:3
标识
DOI:10.24869/psyd.2019.235
摘要

BACKGROUND Previous research showed inconsistent results concerning a possible association between solute carrier family 6 member 3 (SLC6A3) gene polymorphisms and dopamine symptoms of posttraumatic stress disorder (PTSD). Several studies also indicate that the myelin basic protein (MBP) gene is of importance in the etiology of several psychiatric disorders. The aim of this study was to investigate the relation of distinct SLC6A3 and MBP gene polymorphisms with PTSD and whether SLC6A3 and MBP genotypes contribute to PTSD symptom severity. SUBJECTS AND METHODS The study included 719 individuals who had experienced war trauma in the South Eastern Europe (SEE). Genotypes of variable number tandem repeat (VNTR) polymorphism within the SLC6A3 gene were assessed in 696 participants, and the single nucleotide polymorphism (SNP) rs12458282 located within the MBP gene region was genotyped in a total of 703 subjects. The Mini International Neuropsychiatric Interview, the Clinical Administrated PTSD Scale (CAPS) and Brief Symptom Inventory (BSI), were used for data collection. RESULTS No significant differences concerning the investigated SLC6A3 and MBP polymorphisms was identifiable between PTSD and non PTSD participants. Also we could not detect significant influence of these distinct SLC6A3 and MBP alleles on the severity of PTSD symptoms (CAPS) or BSI scores. However, the results of MBP rs12458282 within the patients with lifetime PTSD may point to a possible correlation of the major allele (T) with elevated CAPS scores. CONCLUSIONS Our results do not support an association of the analysed SLC6A3 and MBP gene polymorphisms with PTSD in war traumatized individuals. We found that there is a possibility for a correlation of the T allele rs12458282 within the MBP gene with higher CAPS scores in lifetime PTSD patients which would need to be tested in a sample providing more statistical power.

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