噻加宾治疗广泛性焦虑症:一项以帕罗西汀为阳性对照的随机、开放标签临床试验。

Tiagabine for the treatment of generalized anxiety disorder: a randomized, open-label, clinical trial with paroxetine as a positive control.

作者信息

Rosenthal Murray

机构信息

BMR HealthQuest, 3625 Ruffin Road, Suite 100, San Diego, CA 92123, USA.

出版信息

J Clin Psychiatry. 2003 Oct;64(10):1245-9. doi: 10.4088/jcp.v64n1016.

Abstract

BACKGROUND

Gamma-aminobutyric acid (GABA) plays a central role in the pathophysiology of anxiety. Tiagabine, a selective GABA reuptake inhibitor, enhances normal GABA tone. This 10-week, randomized, open-label trial evaluated tiagabine in patients with generalized anxiety disorder (GAD), with paroxetine serving as a positive control.

METHOD

Adult patients with DSM-IV GAD were randomly assigned to receive either tiagabine or paroxetine. Tiagabine was initiated at 4 mg/day (2 mg morning and evening) during week 1. Between weeks 2 and 6, the dose was individually titrated in 2-mg increments (maximum increase of 4 mg/week) for optimal response to a maximum dose of 16 mg/day (8 mg morning and evening). During weeks 7 through 10, patients received the dosage determined during the titration period. Paroxetine was initiated at 20 mg nightly for the first week and similarly titrated in 10-mg increments to a maximum dose of 60 mg/day. Assessments included the Hamilton Rating Scale for Anxiety (HAM-A), Hospital Anxiety and Depression Scale (HADS), Hamilton Rating Scale for Depression (HAM-D), Pittsburgh Sleep Quality Index (PSQI), and Sheehan Disability Scale (SDS).

RESULTS

Forty patients were enrolled (tiagabine, N = 20; paroxetine, N = 20). Mean final doses were tiagabine 10 mg/day (range, 4-16 mg/day) or paroxetine 27 mg/day (range, 20-40 mg/day). Tiagabine and paroxetine significantly reduced anxiety (HAM-A and HADS total and anxiety subscales). Although patients were not diagnosed with a mood disorder, both tiagabine and paroxetine reduced comorbid depressive symptoms (HAM-D total and HADS total and depressive subscale). Tiagabine and paroxetine significantly improved sleep quality (PSQI) and functioning (SDS). Both tiagabine and paroxetine were well tolerated.

CONCLUSION

The selective GABA reuptake inhibitor tiagabine and the positive control paroxetine significantly reduced anxiety and comorbid depressive symptoms, improved sleep quality and functioning, and were well tolerated in patients with GAD. Tiagabine may be a therapeutic option for the treatment of anxiety disorders.

摘要

背景

γ-氨基丁酸(GABA)在焦虑症的病理生理学中起核心作用。替加宾,一种选择性GABA再摄取抑制剂,可增强正常的GABA张力。这项为期10周的随机开放标签试验评估了替加宾在广泛性焦虑症(GAD)患者中的疗效,以帕罗西汀作为阳性对照。

方法

将符合DSM-IV标准的成年GAD患者随机分配接受替加宾或帕罗西汀治疗。第1周时替加宾起始剂量为4mg/天(早晚各2mg)。在第2至6周期间,剂量以2mg的增量进行个体化滴定(每周最大增加4mg),以达到最佳反应,最大剂量为16mg/天(早晚各8mg)。在第7至10周期间,患者接受滴定期确定的剂量。帕罗西汀第1周每晚起始剂量为20mg,同样以10mg的增量滴定,最大剂量为60mg/天。评估包括汉密尔顿焦虑量表(HAM-A)、医院焦虑抑郁量表(HADS)、汉密尔顿抑郁量表(HAM-D)、匹兹堡睡眠质量指数(PSQI)和希恩功能障碍量表(SDS)。

结果

共纳入40例患者(替加宾组,N = 20;帕罗西汀组,N = 20)。替加宾的平均最终剂量为10mg/天(范围4 - 16mg/天),帕罗西汀为27mg/天(范围20 - 40mg/天)。替加宾和帕罗西汀均显著降低了焦虑(HAM-A和HADS总分及焦虑分量表)。尽管患者未被诊断为情绪障碍,但替加宾和帕罗西汀均减轻了共病的抑郁症状(HAM-D总分及HADS总分和抑郁分量表)。替加宾和帕罗西汀均显著改善了睡眠质量(PSQI)和功能(SDS)。替加宾和帕罗西汀耐受性均良好。

结论

选择性GABA再摄取抑制剂替加宾和阳性对照帕罗西汀均显著降低了焦虑和共病的抑郁症状,改善了睡眠质量和功能,且在GAD患者中耐受性良好。替加宾可能是治疗焦虑症的一种治疗选择。

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