Department of Psychiatry and Behavioral Sciences, University of Kansas School of Medicine-Wichita, Wichita, KS, USA.
Neuropsychiatr Dis Treat. 2009;5:23-31. Epub 2009 Apr 8.
Approximately 16 million people in the United States suffer from anxiety disorders alone, while another 12 million experience both anxiety and at least one other psychiatric condition. Generalized anxiety disorder (GAD) has lifetime prevalence rates between 5% and 6%. Treatment of GAD is aimed primarily at symptom reduction. Duloxetine, a serotonin norepinephrine reuptake inhibitor (SNRI), received Food and Drug Administration (FDA) approval for the treatment of GAD in 2007. This article reviews the pharmacologic profile and seminal clinical trials associated with the FDA indication of duloxetine for GAD. A literature search performed using PubMed with the keywords "duloxetine", "gad", "generalized anxiety disorder", and "venlafaxine XR" yielded 27 articles. We also focused on papers that pooled data from these seminal studies. Data on file from Eli Lilly were also reviewed, including data from the Eli Lilly website. Based on this search, duloxetine was found to be an FDA-approved treatment option for GAD that has been studied in several double-blind, placebo-controlled clinical trials. This review of duloxetine will help physicians to interpret clinical studies properly and also help them to make an informed decision about which patients are the most appropriate candidates for a trial of duloxetine.
大约有 1600 万美国人患有单纯的焦虑症,而另外 1200 万人同时患有焦虑症和至少一种其他精神疾病。广泛性焦虑症(GAD)的终身患病率在 5%至 6%之间。GAD 的治疗主要旨在减轻症状。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),于 2007 年获得美国食品和药物管理局(FDA)批准用于治疗 GAD。本文回顾了与度洛西汀治疗 GAD 的 FDA 适应证相关的药理学特征和关键性临床试验。使用 PubMed 关键词“度洛西汀”、“gad”、“广泛性焦虑症”和“venlafaxine XR”进行文献检索,共得到 27 篇文章。我们还重点关注了汇总这些关键研究数据的论文。还审查了礼来公司的文件数据,包括来自礼来公司网站的数据。根据这项搜索,度洛西汀是一种已在多项双盲、安慰剂对照临床试验中得到研究的 FDA 批准的 GAD 治疗选择。对度洛西汀的这一回顾将帮助医生正确解读临床研究,并帮助他们做出明智的决策,确定哪些患者最适合度洛西汀试验。