Papakostas George I, McGrath Patrick, Stewart Jonathan, Charles Dana, Chen Ying, Mischoulon David, Dording Christina, Fava Maurizio
Depression Clinical and Research Program at Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Psychiatry Res. 2008 Oct 30;161(1):116-20. doi: 10.1016/j.psychres.2008.02.011. Epub 2008 Aug 27.
The purpose of this study was to examine whether the presence/severity of psychic and somatic anxiety symptoms predicted clinical response following a 12-week, flexible-dose (20-60 mg daily), open-label trial of fluoxetine for major depressive disorder (MDD). The presence and severity of psychic and somatic anxiety symptoms were assessed with the use of select subscales of the Symptom Questionnaire and the Hopkins Symptom Checklist among 518 outpatients with MDD. With the use of separate logistic regressions, we tested for the relationship between clinical response, baseline Hamilton Depression Rating Scale (HAM-D-17) scores, and subscale scores at baseline entered separately as independent variables Overall completion, response and remission rates for the trial were 64.2%, 55.4%, and 48.9%, respectively. All subscale scores selected for this analysis significantly predicted treatment response to fluoxetine. The presence/severity of psychic and somatic anxiety symptoms of MDD at baseline predicted an increased likelihood of non-response to fluoxetine in MDD. Studies examining whether specific treatment strategies are more effective than the selective serotonin reuptake inhibitors for MDD patients with high levels of co-morbid psychic and somatic anxiety symptoms are warranted.
本研究的目的是,在一项为期12周、剂量灵活(每日20 - 60毫克)、开放标签的氟西汀治疗重度抑郁症(MDD)试验之后,检验精神性和躯体性焦虑症状的存在/严重程度是否能预测临床反应。在518例MDD门诊患者中,使用症状问卷和霍普金斯症状清单的特定子量表评估精神性和躯体性焦虑症状的存在及严重程度。通过单独的逻辑回归分析,我们分别将临床反应、基线汉密尔顿抑郁量表(HAM-D-17)得分以及基线时的子量表得分作为自变量,检验它们之间的关系。该试验的总体完成率、反应率和缓解率分别为64.2%、55.4%和48.9%。本次分析所选的所有子量表得分均能显著预测对氟西汀的治疗反应。MDD患者基线时精神性和躯体性焦虑症状的存在/严重程度预示着对氟西汀无反应的可能性增加。有必要开展研究,探讨对于伴有高水平共病精神性和躯体性焦虑症状的MDD患者,特定治疗策略是否比选择性5-羟色胺再摄取抑制剂更有效。