The role of pain expectancy and its confidence in placebo hypoalgesia and nocebo hyperalgesia.

IF 5.5 1区 医学 Q1 ANESTHESIOLOGY PAIN® Pub Date : 2025-01-09 DOI:10.1097/j.pain.0000000000003495
Eleonora Maria Camerone, Giorgia Tosi, Daniele Romano
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Abstract

Abstract: Placebo hypoalgesia and nocebo hyperalgesia, which exemplify the impact of expectations on pain, have recently been conceptualised as Bayesian inferential processes, yet empirical evidence remains limited. Here, we explore whether these phenomena can be unified within the same Bayesian framework by testing the predictive role of expectations and their level of precision (ie, expectation confidence) on pain, with both predictors measured at the metacognitive level. Sixty healthy volunteers underwent a pain test (ie, 8 noxious electrical stimuli) before (Baseline) and after (T0, T1, T2) receiving a sham treatment associated with hypoalgesic (placebo), hyperalgesic (nocebo), or neutral (control) verbal suggestions, depending on group allocation. Trial-by-trial expectations, their precision, and perceived pain were measured. Skin conductance response (SCR) was also recorded as an autonomic response marker. Bayesian linear mixed models analyses revealed that, for both placebo and nocebo, pain was predicted by expectations alone and by their interaction with expectations precision. In addition, the discrepancy between expected and perceived pain was predicted by expectation precision, with greater alignment between expected and perceived pain when precision was higher. This suggests that both placebo and nocebo responses are well described from a Bayesian perspective. A main effect of time for SCR was observed, suggesting habituation to painful stimuli. Our data provide evidence indicating that both placebo hypoalgesia and nocebo hyperalgesia can be unified within the same Bayesian framework in which not only expectations but also their level of precision, both measured at the metacognitive level, are key determinants of the pain inferential process.

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疼痛预期及其信心在安慰剂低镇痛和安慰剂高镇痛中的作用。
摘要:安慰剂痛觉减退和反安慰剂痛觉过敏是预期对疼痛影响的例证,最近被概念化为贝叶斯推理过程,但经验证据仍然有限。在这里,我们探讨这些现象是否可以统一在同一个贝叶斯框架内,通过测试预期的预测作用和他们的精度水平(即期望置信度)对疼痛,在元认知水平的预测测量。60名健康志愿者在(基线)之前和之后(T0, T1, T2)接受了疼痛测试(即8次有害电刺激),并根据组分配接受了与低痛觉(安慰剂),高痛觉(反安慰剂)或中性(对照组)口头建议相关的假治疗。每一次试验的期望、精确度和感知的痛苦都被测量。皮肤电导反应(SCR)也被记录为自主反应标志物。贝叶斯线性混合模型分析显示,对于安慰剂和反安慰剂,疼痛仅通过期望和期望精度的相互作用来预测。此外,预期疼痛与感知疼痛之间的差异可以通过期望精度来预测,当精确度越高时,预期疼痛与感知疼痛之间的一致性越强。这表明,从贝叶斯的角度来看,安慰剂和反安慰剂的反应都得到了很好的描述。观察到时间对SCR的主要影响,提示对疼痛刺激的习惯。我们的数据提供的证据表明,安慰剂痛觉减少和反安慰剂痛觉过敏可以统一在同一个贝叶斯框架内,其中不仅期望,而且精度水平,都是在元认知水平上测量的,是疼痛推理过程的关键决定因素。
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来源期刊
PAIN®
PAIN® 医学-临床神经学
CiteScore
12.50
自引率
8.10%
发文量
242
审稿时长
9 months
期刊介绍: PAIN® is the official publication of the International Association for the Study of Pain and publishes original research on the nature,mechanisms and treatment of pain.PAIN® provides a forum for the dissemination of research in the basic and clinical sciences of multidisciplinary interest.
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