Center for Clinical Research, Mercer University, Atlanta, GA, USA.
Int J Gen Med. 2009 Dec 29;2:153-62.
Duloxetine is a serotonin-norepinephrine reuptake inhibitor (SNRI) which is FDA approved for the treatment of generalized anxiety disorder (GAD) in doses of 30 mg to 120 mg daily. Duloxetine has been shown to significantly improve symptoms of GAD as measured through the Hamilton Anxiety Rating Scale (HAMA), the Clinical Global Impressions Scale (CGI-I), and other various outcome measures in several placebo-controlled, randomized, double blind, multi-center studies. Symptom improvement began within the first few weeks, and continued for the duration of the studies. In addition, duloxetine has also been shown to improve outcomes in elderly patients with GAD, and in GAD patients with clinically significant pain symptoms. Duloxetine was noninferior compared with venlafaxine XR. Duloxetine was found to have a good tolerability profile which was predictable and similar to another SNRI, venlafaxine. Adverse events (AEs) such as nausea, constipation, dry mouth, and insomnia were mild and transient, and occurred at relatively low rates. It was found to have a low frequency of drug interactions. In conclusion, duloxetine, a selective inhibitor for the serotonin and norepinephrine transporters, is efficacious in the treatment of GAD, and has a predictable tolerability profile, with AEs generally being mild to moderate.
度洛西汀是一种 5-羟色胺和去甲肾上腺素再摄取抑制剂(SNRI),已被美国食品药品监督管理局(FDA)批准用于治疗广泛性焦虑障碍(GAD),剂量为每天 30 毫克至 120 毫克。多项安慰剂对照、随机、双盲、多中心研究表明,度洛西汀可显著改善 GAD 的症状,如汉密尔顿焦虑量表(HAMA)、临床总体印象量表(CGI-I)和其他各种疗效指标。症状改善始于最初的几周内,并持续整个研究期间。此外,度洛西汀还显示出在老年 GAD 患者和伴有临床显著疼痛症状的 GAD 患者中改善结局的作用。度洛西汀与文拉法辛 XR 相比非劣效。度洛西汀具有良好的耐受性,与另一种 SNRI 文拉法辛的预测性和相似性。不良反应(AEs)如恶心、便秘、口干和失眠均为轻度和短暂的,且发生率相对较低。它发现药物相互作用的频率较低。总之,度洛西汀是一种 5-羟色胺和去甲肾上腺素转运体的选择性抑制剂,在治疗 GAD 方面有效,具有可预测的耐受性,不良反应通常为轻度至中度。