Department of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh.
Diabetes Care. 2011 Apr;34(4):818-22. doi: 10.2337/dc10-1793. Epub 2011 Feb 25.
To compare the efficacy and safety of duloxetine and amitriptyline in painful diabetic neuropathy (PDN).
In this randomized, double-blind, cross-over, active-control trial, 58 patients received amitriptyline and duloxetine orally once daily at bedtime, each for 6 weeks with optional dose uptitration fortnightly. Single-blinded placebo washout was given for 2 weeks between the two treatments and a single-blinded placebo run-out phase of 4 weeks was given at the end of the treatment period. Pain relief was measured by the patient's global assessment of efficacy, using a visual analog scale (0-100) as a primary end point, and overall improvement and adverse events were assessed as secondary outcome measures. Median pain score reductions of >50%, 25-50%, and <25% were considered good, moderate, and mild responses, respectively.
There was a significant improvement in pain with both treatments compared with their baseline values (P < 0.001 for both). Good, moderate, and mild pain relief was achieved in 55, 24, and 15% of patients, respectively, on amitriptyline and 59, 21, and 9% of patients, respectively, on duloxetine. There were no significant differences in various other outcome measures between the groups. Of the reported adverse events, dry mouth was significantly more common with amitriptyline than duloxetine (55 vs. 24%; P < 0.01). Although, numerically, more patients preferred duloxetine, overall this was not statistically significant (48 vs. 36%; P = 0.18).
Both duloxetine and amitriptyline demonstrated similar efficacy in PDN. A large, multicentric clinical trial in other populations could possibly demonstrate the superiority of either drug.
比较度洛西汀与阿米替林治疗痛性糖尿病周围神经病变(PDN)的疗效和安全性。
本随机、双盲、交叉、阳性对照试验共纳入 58 例患者,他们每晚口服度洛西汀或阿米替林,剂量均为起始 1 次/d,6 周后可选择两周加量 1 次。两种治疗方案之间给予单盲安慰剂洗脱 2 周,治疗期末给予单盲安慰剂洗脱 4 周。主要终点为患者整体疗效的视觉模拟评分(0-100),次要终点为总体改善和不良反应。
与基线相比,两种药物治疗均可显著缓解疼痛(均 P < 0.001)。阿米替林组和度洛西汀组分别有 55%、24%和 15%的患者疼痛缓解程度为“很好”、“中度”和“轻度”,59%、21%和 9%的患者疼痛缓解程度为“很好”、“中度”和“轻度”。两组间其他各项结局指标均无显著差异。报告的不良反应中,阿米替林组口干发生率显著高于度洛西汀组(55%比 24%,P < 0.01)。尽管从数值上看,更多的患者更喜欢度洛西汀,但总体上这并不具有统计学意义(48%比 36%,P = 0.18)。
度洛西汀与阿米替林治疗 PDN 的疗效相似。在其他人群中开展更大规模的多中心临床试验,可能会显示出两种药物中任一种药物的优势。