Center for Clinical Research, Mercer University, Atlanta, Georgia, USA.
J Pain Res. 2010 Dec 16;4:1-10. doi: 10.2147/JPR.S12866.
Duloxetine is a serotonin-norepinephrine reuptake inhibitor approved by the US Food and Drug Administration for the treatment of fibromyalgia and painful diabetic neuropathy at doses of 60 mg daily. Duloxetine has been shown to significantly improve the symptoms of chronic pain associated with these disorders, as measured by the Fibromyalgia Impact Questionnaire, Brief Pain Inventory scores, the Clinical Global Impressions Scale, and other various outcome measures in several placebo-controlled, randomized, double-blind, multicenter studies. Symptom improvement generally began within the first few weeks, and continued for the duration of the study. In addition, the efficacy of duloxetine was found to be due to direct effects on pain symptoms rather than secondary to improvements in depression or anxiety. Adverse events including nausea, constipation, dry mouth, and insomnia, were mild and transient and occurred at relatively low rates. In conclusion, duloxetine, a selective inhibitor for the serotonin and norepinephrine transporters, is efficacious in the treatment of chronic pain associated with fibromyalgia or diabetic neuropathy, and has a predictable tolerability profile, with adverse events 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,已被美国食品药品监督管理局批准用于治疗纤维肌痛和糖尿病性周围神经痛,剂量为每日 60 毫克。度洛西汀已被证明能显著改善这些疾病相关慢性疼痛的症状,如纤维肌痛影响问卷、简明疼痛量表评分、临床总体印象量表和其他几项安慰剂对照、随机、双盲、多中心研究中的各种结果测量。症状改善一般在最初几周内开始,并持续整个研究期间。此外,度洛西汀的疗效似乎是由于对疼痛症状的直接作用,而不是继发于抑郁或焦虑的改善。包括恶心、便秘、口干和失眠在内的不良事件均为轻度和短暂,且发生率相对较低。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,在治疗纤维肌痛或糖尿病性周围神经痛相关的慢性疼痛方面有效,且具有可预测的耐受性,其不良事件通常为轻至中度。