Meyers Elke, Della Porta Delia, Torta Diana M, van den Broeke Emanuel N
Health Psychology, Faculty of Psychology and Educational Sciences, KU Leuven, Leuven, Belgium.
Institute of Neuroscience, Faculty of Medicine, UCLouvain, Louvain-la-Neuve, Belgium.
Pain Rep. 2025 May 27;10(4):e1291. doi: 10.1097/PR9.0000000000001291. eCollection 2025 Aug.
As central sensitization is believed to contribute to persistent pain and psychological factors are increasingly acknowledged to play a role as well, the question arises of whether psychological factors can modulate the development of central sensitization. Secondary hyperalgesia is thought to be a manifestation of central sensitization and can be induced experimentally in humans. To define the state-of-the-art, we critically reviewed the existing evidence that psychological factors can influence the development of experimentally induced secondary hyperalgesia, a proxy of central sensitization. We retrieved 23 studies, 17 aimed at modulating the development of secondary hyperalgesia, 4 at modulating hyperalgesia when already established, and 2 observational studies. The psychological interventions in the 17 included papers focused on placebo/nocebo interventions (N = 5), attention and cognitive load (N = 6, 7 experiments), social support (N = 1), cognitive behavioral therapy (N = 1), threat/fear induction (N = 2), and emotional disclosure (N = 1). Interventions were considered effective if they successfully decreased or increased the magnitude and/or spatial extent of secondary hyperalgesia. Although some psychological manipulations might interfere with the development of secondary hyperalgesia, the number of studies is too low to draw firm conclusions. More studies and replications are needed to determine the impact of psychological factors on the development of secondary hyperalgesia. Factors that should be considered in future studies are (among others) the risk of bias, sufficient statistical power, the measurement of secondary hyperalgesia, the choice of sensitization protocol, the strength of the manipulation, and the role of sex.
由于中枢敏化被认为会导致持续性疼痛,并且心理因素在其中所起的作用也越来越受到认可,因此就出现了心理因素是否能够调节中枢敏化发展的问题。继发性痛觉过敏被认为是中枢敏化的一种表现,并且可以在人体中通过实验诱导产生。为了明确最新情况,我们严格审查了现有证据,即心理因素能够影响实验诱导的继发性痛觉过敏(中枢敏化的一个替代指标)的发展。我们检索到23项研究,其中17项旨在调节继发性痛觉过敏的发展,4项旨在调节已经形成的痛觉过敏,还有2项观察性研究。在这17篇纳入的论文中,心理干预措施主要集中在安慰剂/反安慰剂干预(N = 5)、注意力和认知负荷(N = 6,7项实验)、社会支持(N = 1)、认知行为疗法(N = 1)、威胁/恐惧诱导(N = 2)以及情感表露(N = 1)。如果干预措施成功降低或增加了继发性痛觉过敏的程度和/或空间范围,那么这些干预措施就被认为是有效的。尽管一些心理操纵可能会干扰继发性痛觉过敏的发展,但研究数量过少,无法得出确凿结论。需要更多的研究和重复实验来确定心理因素对继发性痛觉过敏发展的影响。未来研究中应考虑的因素(包括但不限于)有偏倚风险、足够的统计效力、继发性痛觉过敏的测量、敏化方案的选择、操纵的强度以及性别的作用。