Opioids Diminish the Placebo Antidepressant Response: A Post Hoc Analysis of a Randomized Controlled Ketamine Trial.

Theresa R Lii, Josephine R Flohr, Robin L Okada, Lisa J Cianfichi, Laura M Hack, Alan F Schatzberg, Boris D Heifets
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Abstract

Background: The endogenous opioid system is thought to play a role in the placebo antidepressant response. A recent trial comparing the rapid antidepressant effects of ketamine versus placebo in surgical patients, some of whom were on chronic opioid therapy, revealed a substantial placebo effect. This finding provided an opportunity to test the hypothesis that opioid agonist exposure interacts with placebo antidepressant responses.

Methods: This post hoc analysis utilized data from a previously reported randomized, anesthesia-blinded, placebo-controlled trial of intravenous ketamine in depressed patients undergoing routine surgery. Mixed-effects models were used to determine whether baseline opioid use influenced antidepressant responses to the trial interventions, as measured by the Montgomery-Åsberg Depression Rating Scale (MADRS) over 1 to 14 days post-treatment.

Results: In the placebo arm, baseline opioid use was associated with a 10-point increase (95% CI: 0.81-19.4) in MADRS scores across all post-treatment time points, indicating worse depression in this subgroup. In an alternative model using percent change in MADRS scores, the difference between opioid users and non-users was 38.4% (95% CI: 8.59-68.2), with opioid users experiencing less improvement. For ketamine-treated participants, baseline opioid use did not significantly impact MADRS scores or the percent change in MADRS scores. Pain intensity was not a significant predictor of MADRS outcomes, and the correlation between post-treatment MADRS scores and pain intensity was negligible (R=0.12).

Limitations: This analysis was unregistered and conducted on a small sample; the findings need to be confirmed by prospective controlled studies.

Conclusions: Opioid use at baseline attenuated the placebo antidepressant response independently of pain in depressed patients who received the study treatment under general anesthesia for routine surgery. The antidepressant response was preserved in opioid users who received intravenous ketamine.

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阿片类药物会降低安慰剂抗抑郁反应:氯胺酮随机对照试验的事后分析。
背景:内源性阿片系统被认为在安慰剂抗抑郁反应中发挥了作用。最近的一项试验比较了氯胺酮和安慰剂对外科手术患者的快速抗抑郁作用,结果显示安慰剂效应非常明显。这一发现为检验阿片类激动剂暴露与安慰剂抗抑郁反应相互作用的假设提供了机会:这项事后分析利用了之前报道过的一项随机、麻醉盲、安慰剂对照试验的数据,该试验对接受常规手术的抑郁症患者进行静脉注射氯胺酮治疗。结果显示,基线阿片类药物的使用是否会影响对试验干预措施的抗抑郁反应(以治疗后1至14天的蒙哥马利-阿斯伯格抑郁评定量表(MADRS)来衡量):分析结果表明,基线阿片类药物的使用显著降低了接受安慰剂治疗的患者的治疗后抑郁严重程度,但没有降低接受氯胺酮治疗的患者的抑郁严重程度。这种降低与基线抑郁严重程度、基线疼痛强度和种族无关。此外,术后疼痛强度与抑郁严重程度之间的相关性微乎其微:局限性:该分析未经注册,且样本较少;研究结果需要前瞻性对照研究加以证实:结论:在常规手术全身麻醉下接受研究治疗的抑郁症患者,基线使用阿片类药物会减弱安慰剂抗抑郁反应,而与疼痛无关。静脉注射氯胺酮的阿片类药物使用者的抗抑郁反应保持不变。
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