Radbourne Unit, Derby City General Hospital, Uttoxeter Rd, Derby DE22 3NE, United Kingdom.
J Clin Psychiatry. 2013 Jun;74(6):587-94. doi: 10.4088/JCP.12m08250.
The present placebo-controlled study evaluated the efficacy, tolerability, and safety of 8-week treatment with agomelatine (25-50 mg/d by mouth) in elderly patients with major depressive disorder (MDD).
Elderly outpatients aged ≥ 65 years with a primary diagnosis of moderate to severe episode of recurrent MDD (DSM-IV-TR) were recruited in 27 clinical centers in Argentina, Finland, Mexico, Portugal, and Romania from November 2009 to October 2011. The primary outcome measure was the 17-item Hamilton Depression Rating Scale (HDRS17) total score.
A total of 222 elderly patients entered the study (151 in the agomelatine group, 71 in the placebo group), including 69 patients aged 75 years and older. Agomelatine improved depressive symptoms in the elderly population, as evaluated by the HDRS17 total score, in terms of last postbaseline value (agomelatine-placebo difference: mean estimate [standard error] = 2.67 [1.06] points; P = .013) and response to treatment (agomelatine, 59.5%; placebo, 38.6%; P = .004). The agomelatine-placebo difference according to the Clinical Global Impressions-Severity of Illness scale (CGI-S) score was 0.48 (0.19). The agomelatine-placebo difference (estimate [standard error]) for remission on the HDRS17 was 6.9% (4.7%) and did not achieve statistical significance (P = .179, post hoc analysis). Clinically relevant effects of agomelatine were confirmed on all end points in the subset of severely depressed patients (HDRS17 total score ≥ 25 and CGI-S score ≥ 5 at baseline). Agomelatine was well tolerated by patients, with only minimal distinctions from placebo.
The present study provides the first evidence that an 8-week treatment with agomelatine 25-50 mg/d efficiently relieves depressive symptoms and is well tolerated in elderly depressed patients older than 65 years.
Controlled-Trials.com identifier: ISRCTN57507360.
本安慰剂对照研究评估了 8 周阿戈美拉汀(25-50mg/d 口服)治疗老年重性抑郁障碍(MDD)患者的疗效、耐受性和安全性。
2009 年 11 月至 2011 年 10 月,在阿根廷、芬兰、墨西哥、葡萄牙和罗马尼亚的 27 个临床中心招募了年龄≥65 岁、原发性诊断为中度至重度复发性 MDD(DSM-IV-TR)的老年门诊患者。主要结局测量指标为 17 项汉密尔顿抑郁量表(HDRS17)总分。
共有 222 名老年患者进入研究(阿戈美拉汀组 151 例,安慰剂组 71 例),其中 69 例患者年龄≥75 岁。阿戈美拉汀改善了老年人群的抑郁症状,HDRS17 总分的最后一次基线后值评估显示,阿戈美拉汀与安慰剂的差异为 2.67(1.06)分(P =.013),且治疗应答率差异显著(阿戈美拉汀组 59.5%,安慰剂组 38.6%;P =.004)。根据临床总体印象-严重程度量表(CGI-S)评分,阿戈美拉汀与安慰剂的差异为 0.48(0.19)分。HDRS17 缓解的阿戈美拉汀与安慰剂的差异(估计值[标准误差])为 6.9%(4.7%),但未达到统计学显著性(P =.179,事后分析)。在基线时 HDRS17 总分≥25 分且 CGI-S 评分≥5 分的重度抑郁患者亚组中,阿戈美拉汀在所有终点上均显示出具有临床意义的疗效。阿戈美拉汀在老年患者中耐受性良好,与安慰剂相比仅有最小差异。
本研究首次提供了 8 周阿戈美拉汀 25-50mg/d 治疗能有效缓解老年抑郁患者抑郁症状的证据,且 65 岁以上老年抑郁患者耐受性良好。
ClinicalTrials.gov 标识符:ISRCTN57507360。