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首页> 外文期刊>Biological psychiatry >Preliminary evidence of the short allele of the serotonin transporter gene predicting poor response to cognitive behavior therapy in posttraumatic stress disorder.
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Preliminary evidence of the short allele of the serotonin transporter gene predicting poor response to cognitive behavior therapy in posttraumatic stress disorder.

机译:5-羟色胺转运蛋白基因短等位基因的初步证据预示了创伤后应激障碍对认知行为疗法的不良反应。

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OBJECTIVE: This study was intended to assess the extent to which the low-expression alleles of the serotonin transporter gene promoter predict poor response to cognitive behavior therapy in patients with posttraumatic stress disorder (PTSD). METHOD: Forty-five patients with PTSD underwent an 8-week exposure-based cognitive behavior therapy program and provided mouth swabs or saliva samples to extract genomic DNA and classify individuals according to four allelic forms (S(A), S(G), L(A), L(G)) of the 5-HTT-linked polymorphic region (5-HTTLPR). We determined whether the 5-HTTLPR genotype predicted change in PTSD severity following treatment (n = 45) and 6 months later (n = 42). RESULTS: After controlling for pretreatment PTSD severity and number of treatment sessions, the 5-HTTLPR low-expression genotype group (S or L(G) allele carriers) displayed more severe PTSD 6 months following treatment relative to other patients. CONCLUSIONS: This study suggests a genetic contribution to treatment outcome following cognitive behavior therapy and implicates the serotonergic system in response to exposure-based treatments in PTSD.
机译:目的:本研究旨在评估5-羟色胺转运蛋白基因启动子的低表达等位基因预测创伤后应激障碍(PTSD)患者对认知行为疗法的不良反应的程度。方法:45名创伤后应激障碍患者接受了为期8周的基于暴露的认知行为治疗计划,并提供了拭子或唾液样本以提取基因组DNA并根据四种等位基因形式对个体进行分类(S(A),S(G), 5-HTT连接的多态性区域(5-HTTLPR)的L(A),L(G))。我们确定5-HTTLPR基因型是否可以预测治疗后(n = 45)和6个月后(n = 42)的PTSD严重性变化。结果:在控制了治疗前PTSD的严重程度和治疗次数之后,相对于其他患者,治疗后6个月的5-HTTLPR低表达基因型组(S或L(G)等位基因携带者)表现出更严重的PTSD。结论:这项研究提示认知行为疗法后遗传对治疗结果的贡献,并暗示对PTSD中基于暴露的疗法有反应的血清素能系统。

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