Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, China.
Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jul 1;44:296-300. doi: 10.1016/j.pnpbp.2013.04.004. Epub 2013 Apr 10.
Stathmin (STMN1) has been demonstrated as a regulator of fear processing across species, which implicates that it may be important in the etiopathogenesis of fear-related psychiatric disorders such as posttraumatic stress disorder (PTSD). This study examined the association between STMN1 rs182455 genotype, a single nucleotide polymorphism (SNP) located within or close to the putative transcriptional control region of STMN1 gene, and PTSD symptoms. A total of 326 Chinese adults who suffered from a deadly 2008 Wenchuan earthquake and unexpectedly lost their children during the disaster participated in this study. PTSD symptoms were measured with the PTSD Checklist (PCL). The Sequenom iPlex chemistries and the MassARRAY system were used to genotype the STMN1 rs182455 SNP. Our results indicated that the STMN1rs182455 genotype was not associated with severity of total PTSD symptoms in either females or males; however, it could significantly predict severity of PTSD's reexperiencing symptoms in females. The findings provide preliminary evidence supporting the important role of STMN1 in the development of PTSD, and expand extant knowledge on the genetic underpinnings of PTSD and the sex-specific expression of PTSD's symptoms.
Stathmin(STMN1)已被证明是跨物种恐惧处理的调节剂,这表明它可能在创伤后应激障碍(PTSD)等与恐惧相关的精神疾病的发病机制中很重要。本研究探讨了 STMN1 rs182455 基因型(位于 STMN1 基因的假定转录调控区域内或附近的单核苷酸多态性(SNP))与 PTSD 症状之间的关联。共有 326 名中国成年人在 2008 年汶川地震中遭受了致命打击,并在灾难中意外失去了孩子,他们参加了这项研究。使用 PTSD 检查表(PCL)测量 PTSD 症状。使用 Sequenom iPlex 化学和 MassARRAY 系统对 STMN1 rs182455 SNP 进行基因分型。我们的研究结果表明,STMN1rs182455 基因型与女性或男性 PTSD 总症状的严重程度均无关;然而,它可以显著预测女性 PTSD 再体验症状的严重程度。这些发现提供了初步证据,支持 STMN1 在 PTSD 发展中的重要作用,并扩展了 PTSD 的遗传基础以及 PTSD 症状的性别特异性表达的现有知识。