Yehuda Rachel, Blair William, Labinsky Ellen, Bierer Linda M
Department of Psychiatry, Mount Sinai School of Medicine and Bronx Veterans Affairs, 130 West Kingsbridge Rd., Bronx, NY 10468, USA.
Am J Psychiatry. 2007 Jan;164(1):163-6. doi: 10.1176/ajp.2007.164.1.163.
The authors used a low-dose dexamethasone suppression test to examine the effect of a PTSD risk factor, parental PTSD, on cortisol negative feedback inhibition in adult offspring of Holocaust survivors with PTSD (N=13) versus without PTSD (N=12) as well as a comparison group of offspring whose parents had no Holocaust exposure (N=16).
Blood samples were obtained at 8:00 a.m. for the determination of baseline cortisol. Participants ingested 0.5 mg of dexamethasone at 11:00 p.m., and blood samples were obtained again at 8:00 a.m. the following day.
Enhanced cortisol suppression in response to dexamethasone was associated primarily with parental PTSD status, with minimal contribution of subjects' own trauma-related symptoms.
Enhanced cortisol negative feedback inhibition may be associated with PTSD because it is related to the PTSD risk factor of parental PTSD.
作者采用低剂量地塞米松抑制试验,研究创伤后应激障碍(PTSD)的一个风险因素——父母患PTSD,对有PTSD的大屠杀幸存者成年后代(N = 13)与无PTSD的大屠杀幸存者成年后代(N = 12)以及父母未经历大屠杀的后代对照组(N = 16)中皮质醇负反馈抑制的影响。
上午8点采集血样以测定基础皮质醇水平。参与者于晚上11点摄入0.5毫克地塞米松,并于次日上午8点再次采集血样。
地塞米松引起的皮质醇抑制增强主要与父母的PTSD状态有关,而受试者自身与创伤相关的症状影响极小。
皮质醇负反馈抑制增强可能与PTSD有关,因为它与父母患PTSD这一PTSD风险因素相关。