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氟西汀与贞节树提取物治疗经前烦躁障碍的对比研究

Fluoxetine versus Vitex agnus castus extract in the treatment of premenstrual dysphoric disorder.

作者信息

Atmaca Murad, Kumru Selahattin, Tezcan Ertan

机构信息

Firat University, School of Medicine, Department of Psychiatry, Elazig, Turkey.

出版信息

Hum Psychopharmacol. 2003 Apr;18(3):191-5. doi: 10.1002/hup.470.

Abstract

Clinical trials have demonstrated that serotonin reuptake inhibitors (SRIs) and the extract of Vitex agnus castus are effective for the treatment of premenstrual dysphoric disorder (PMDD). However, to the best of our knowledge, there has been no study comparing the efficacy of the SRIs with Vitex agnus castus (AC) extract. Therefore, the aim of the present study was to compare the efficacy of fluoxetine, a selective serotonin reuptake inhibitor (SSRI), with that of the AC extract, a natural choice. After a period of 2 screening months to screen the patients for suitability, 41 patients with PMDD according to DSM-IV were recruited into the study. The patients were randomized to fluoxetine or AC for 2 months of single-blind, rater- blinded and prospective treatment period. The outcome measures included the Penn daily symptom report (DSR), the Hamilton depression rating scale (HAM-D), and the clinical global impression-severity of illness (CGI-SI) and -improvement (CGI-I) scales. At endpoint, using the clinical criterion for improvement, a similar percentage of patients responded to fluoxetine (68.4%, n = 13) and AC (57.9%, n = 11). There was no statistically significant difference between the groups with respect to the rate of responders. This preliminary study suggests that patients with PMDD respond well to treatment with both fluoxetine and AC. However, fluoxetine was more effective for psychological symptoms while the extract diminished the physical symptoms.

摘要

临床试验表明,5-羟色胺再摄取抑制剂(SRIs)和贞洁树提取物对经前烦躁障碍(PMDD)的治疗有效。然而,据我们所知,尚无研究比较SRIs与贞洁树(AC)提取物的疗效。因此,本研究的目的是比较选择性5-羟色胺再摄取抑制剂(SSRI)氟西汀与天然药物AC提取物的疗效。经过2个月的筛选期以筛选适合的患者后,41例符合DSM-IV标准的PMDD患者被纳入研究。患者被随机分为氟西汀组或AC组,进行为期2个月的单盲、评分者盲法和前瞻性治疗。疗效指标包括宾夕法尼亚每日症状报告(DSR)、汉密尔顿抑郁量表(HAM-D)以及临床总体印象-疾病严重程度(CGI-SI)和-改善程度(CGI-I)量表。在研究终点,根据临床改善标准,氟西汀组(68.4%,n = 13)和AC组(57.9%,n = 11)的患者缓解比例相似。两组之间的缓解率无统计学显著差异。这项初步研究表明,PMDD患者对氟西汀和AC治疗均反应良好。然而,氟西汀对心理症状更有效,而提取物对躯体症状的改善更明显。

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