Giordano Rocco, Arendt-Nielsen Lars, Gerra Maria Carla, Kappel Andreas, Østergaard Svend Erik, Capriotti Camila, Dallabona Cristina, Petersen Kristian Kjær-Staal
Department of Oral and Maxillofacial Surgery, Aalborg University Hospital, Aalborg, Denmark.
Center for Neuroplasticity and Pain (CNAP), SMI®, Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Pain. 2025 Apr 1;166(4):847-857. doi: 10.1097/j.pain.0000000000003410. Epub 2024 Sep 18.
Chronic postoperative pain is present in approximately 20% of patients undergoing total knee arthroplasty. Studies indicate that pain mechanisms are associated with development and maintenance of chronic postoperative pain. The current study assessed pain sensitivity, inflammation, microRNAs, and psychological factors and combined these in a network to describe chronic postoperative pain. This study involved 75 patients with and without chronic postoperative pain after total knee arthroplasty. Clinical pain intensity, Oxford Knee Score, and pain catastrophizing were assessed as clinical parameters. Quantitative sensory testing was assessed to evaluate pain sensitivity and microRNAs, and inflammatory markers were likewise analyzed. Supervised multivariate data analysis with "Data Integration Analysis for Biomarker Discovery" using Latent cOmponents (DIABLO) was used to describe the chronic postoperative pain intensity. Two DIABLO models were constructed by dividing the patients into 3 groups or 2 defined by clinical pain intensities. Data Integration Analysis for Biomarker discovery using Latent cOmponents model explained chronic postoperative pain and identified factors involved in pain mechanistic networks among assessments included in the analysis. Developing models of 3 or 2 patient groups using the assessments and the networks could explain 81% and 69% of the variability in clinical postoperative pain intensity. The reduction of the number of parameters stabilized the models and reduced the explanatory value to 69% and 51%. This is the first study to use the DIABLO model for chronic postoperative pain and to demonstrate how different pain mechanisms form a pain mechanistic network. The complex model explained 81% of the variability of clinical pain intensity, whereas the less complex model explained 51% of the variability of clinical pain intensity.
慢性术后疼痛在大约20%的全膝关节置换术患者中存在。研究表明,疼痛机制与慢性术后疼痛的发生和维持有关。本研究评估了疼痛敏感性、炎症、微小RNA和心理因素,并将这些因素整合到一个网络中以描述慢性术后疼痛。本研究纳入了75例全膝关节置换术后有或无慢性术后疼痛的患者。评估临床疼痛强度、牛津膝关节评分和疼痛灾难化作为临床参数。进行定量感觉测试以评估疼痛敏感性和微小RNA,并同样分析炎症标志物。使用潜在成分的“生物标志物发现数据整合分析”(DIABLO)进行监督多变量数据分析,以描述慢性术后疼痛强度。通过将患者分为3组或根据临床疼痛强度定义的2组来构建两个DIABLO模型。使用潜在成分模型的生物标志物发现数据整合分析解释了慢性术后疼痛,并在分析中纳入的评估中确定了参与疼痛机制网络的因素。使用这些评估和网络建立3组或2组患者模型可以解释临床术后疼痛强度变异性的81%和69%。参数数量的减少使模型稳定,并将解释值降低到69%和51%。这是第一项使用DIABLO模型研究慢性术后疼痛并展示不同疼痛机制如何形成疼痛机制网络的研究。复杂模型解释了临床疼痛强度变异性的81%,而较简单模型解释了临床疼痛强度变异性的51%。