Department of Physical Therapy and Rehabilitation Science, Carver College of Medicine, University of Iowa, Iowa City, IA.
Department of Psychological and Brain Sciences, Dartmouth College, Hanover, NH.
Pain. 2023 Sep 1;164(9):1912-1926. doi: 10.1097/j.pain.0000000000002938. Epub 2023 Jun 15.
Chronic pain affects more than 50 million Americans. Treatments remain inadequate, in large part, because the pathophysiological mechanisms underlying the development of chronic pain remain poorly understood. Pain biomarkers could potentially identify and measure biological pathways and phenotypical expressions that are altered by pain, provide insight into biological treatment targets, and help identify at-risk patients who might benefit from early intervention. Biomarkers are used to diagnose, track, and treat other diseases, but no validated clinical biomarkers exist yet for chronic pain. To address this problem, the National Institutes of Health Common Fund launched the Acute to Chronic Pain Signatures (A2CPS) program to evaluate candidate biomarkers, develop them into biosignatures, and discover novel biomarkers for chronification of pain after surgery. This article discusses candidate biomarkers identified by A2CPS for evaluation, including genomic, proteomic, metabolomic, lipidomic, neuroimaging, psychophysical, psychological, and behavioral measures. Acute to Chronic Pain Signatures will provide the most comprehensive investigation of biomarkers for the transition to chronic postsurgical pain undertaken to date. Data and analytic resources generatedby A2CPS will be shared with the scientific community in hopes that other investigators will extract valuable insights beyond A2CPS's initial findings. This article will review the identified biomarkers and rationale for including them, the current state of the science on biomarkers of the transition from acute to chronic pain, gaps in the literature, and how A2CPS will address these gaps.
慢性疼痛影响了超过 5000 万的美国人。治疗方法仍然不足,很大程度上是因为慢性疼痛发展背后的病理生理机制仍未被充分理解。疼痛生物标志物有可能识别和测量被疼痛改变的生物途径和表型表达,深入了解生物治疗靶点,并帮助识别有风险的患者,他们可能受益于早期干预。生物标志物被用于诊断、跟踪和治疗其他疾病,但目前还没有用于慢性疼痛的经过验证的临床生物标志物。为了解决这个问题,美国国立卫生研究院共同基金启动了急性到慢性疼痛特征(A2CPS)计划,以评估候选生物标志物,将其发展为生物标志物,并发现手术后疼痛慢性化的新生物标志物。本文讨论了 A2CPS 确定的用于评估的候选生物标志物,包括基因组、蛋白质组、代谢组、脂质组、神经影像学、心理物理学、心理学和行为测量。急性到慢性疼痛特征将提供迄今为止对手术后慢性疼痛转变的生物标志物的最全面研究。A2CPS 生成的数据和分析资源将与科学界共享,希望其他研究人员能够从 A2CPS 的初步发现中提取有价值的见解。本文将回顾已确定的生物标志物和纳入它们的理由、从急性到慢性疼痛转变的生物标志物的现有科学状况、文献中的差距,以及 A2CPS 将如何解决这些差距。