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一项随机、安慰剂对照的 2 期临床试验中成年人重度抑郁症患者报告的与健康相关的生活质量

Patient-reported health-related quality of life from a randomized, placebo-controlled phase 2 trial of zuranolone in adults with major depressive disorder.

机构信息

Sage Therapeutics, Inc., Cambridge, MA, United States of America.

Optum, Johnston, RI, United States of America.

出版信息

J Affect Disord. 2022 Jul 1;308:19-26. doi: 10.1016/j.jad.2022.03.068. Epub 2022 Apr 2.

Abstract

BACKGROUND

Major depressive disorder (MDD), a disabling, potentially life-threatening condition, negatively affects health-related quality of life (HRQoL). This secondary analysis aimed to understand the impact of the neuroactive steroid zuranolone on HRQoL using the Short Form-36v2 Health Survey (SF-36v2).

METHODS

Adult patients with MDD and 17-item Hamilton Rating Scale for Depression total score ≥22 were randomized 1:1 to receive zuranolone 30 mg or placebo for 2 weeks, with 4 weeks follow-up. SF-36v2 scores were assessed at Day 15 across 8 domains (Physical Functioning, Role Physical, Bodily Pain, General Health, Vitality, Social Functioning, Role Emotional, and Mental Health) and 2 summary scores (Physical and Mental Component), using a mixed-effects model for repeated measures. Correlations between SF-36v2 scores and clinician-reported efficacy endpoints were assessed using Pearson's correlation.

RESULTS

Eighty-nine patients were treated with zuranolone 30 mg (n = 45) or placebo (n = 44). In zuranolone-treated patients, HRQoL improved across all SF-36v2 domains and summary scores at Day 15. Improvements exceeding established minimally important difference thresholds were observed in Bodily Pain, General Health, Vitality, Social Functioning, Role Emotional, and Mental Health scores. Improvements in General Health, Vitality, Mental Health, and Mental Component Summary were statistically significant versus placebo (p ≤ 0.025). Clinician-rated endpoints negatively correlated with SF-36v2 scores.

LIMITATIONS

The small unipolar depression sample may not be representative of all US MDD patients. HRQoL measures could be impacted by factors unrelated to depression.

CONCLUSIONS

Zuranolone-treated patients reported rapid and significant improvements in HRQoL versus placebo at Day 15. HRQoL improvements correlated with improvements in clinician-rated assessments.

TRIAL REGISTRATION

clinicaltrials.gov:NCT03000530; https://clinicaltrials.gov/ct2/show/NCT03000530.

摘要

背景

重度抑郁症(MDD)是一种使人丧失能力且可能危及生命的疾病,会对健康相关生活质量(HRQoL)产生负面影响。本二次分析旨在使用健康调查简表 36 项版本 2(SF-36v2)了解神经活性甾体唑拉酮对 HRQoL 的影响。

方法

患有 MDD 的成年患者且 17 项汉密尔顿抑郁量表总分≥22 分,按 1:1 随机分配接受唑拉酮 30mg 或安慰剂治疗 2 周,随后进行 4 周随访。在第 15 天,使用重复测量混合效应模型评估 SF-36v2 8 个领域(身体功能、身体角色、躯体疼痛、总体健康、活力、社会功能、情绪角色和心理健康)和 2 个综合评分(身体和心理成分)的得分。使用 Pearson 相关分析评估 SF-36v2 评分与临床医生报告的疗效终点之间的相关性。

结果

89 例患者接受唑拉酮 30mg 治疗(n=45)或安慰剂治疗(n=44)。在唑拉酮治疗的患者中,在第 15 天所有 SF-36v2 领域和综合评分的 HRQoL 均得到改善。在躯体疼痛、总体健康、活力、社会功能、情绪角色和心理健康评分方面,观察到超过既定最小重要差异阈值的改善。与安慰剂相比,在总体健康、活力、心理健康和心理成分综合评分方面的改善具有统计学意义(p≤0.025)。临床医生评定的终点与 SF-36v2 评分呈负相关。

局限性

小样本单相抑郁症患者可能不能代表所有美国 MDD 患者。HRQoL 测量可能会受到与抑郁无关的因素的影响。

结论

与安慰剂相比,唑拉酮治疗的患者在第 15 天报告了 HRQoL 的快速且显著改善。HRQoL 的改善与临床医生评定的改善相关。

试验注册

clinicaltrials.gov:NCT03000530;https://clinicaltrials.gov/ct2/show/NCT03000530。

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