School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences, Monash University, Clayton, Victoria, Australia; Pain Management and Research Centre, Caulfield Hospital, Caulfield, Victoria, Australia.
Section for Translation Psychobiology in Child and Adolescent Psychiatry, Department of Child and Adolescent Psychiatry, Centre for Psychosocial Medicine, University of Heidelberg, Heidelberg, Germany; University Hospital of Child and Adolescent Psychiatry and Psychotherapy, University of Bern, Bern, Switzerland.
Int J Psychophysiol. 2018 Sep;131:37-43. doi: 10.1016/j.ijpsycho.2018.02.017. Epub 2018 Mar 2.
Previous research has suggested that heart rate variability (HRV; the variability in the interval between successive heartbeats) can predict the perception of experimentally-induced pain (i.e., pain sensitivity). However, little research has sought to investigate sex-specific associations between HRV and pain sensitivity. This is an important consideration, given that sex differences in resting HRV have been observed, and there has been extensive debate about sex differences in sensitivity to experimentally-induced pain. We examined whether the association between resting HRV and sensitivity to experimentally-induced pain differed in men and women. Fifty-one pain free individuals (26 women, mean age = 21.9 years) participated. Resting electrocardiography (ECG) was collected during a paced breathing task (15 cycles per minute), and measures of HRV were extracted via Fast Fourier Transformation. Thermal heat pain threshold (i.e., the point at which the sensation was first perceived as painful, rather than warm) was measured with a Medoc Pathway Pain and Sensory Evaluation System. There were no sex differences in resting HRV or thermal heat pain threshold, nor did sex moderate the relationship between HRV and thermal heat pain threshold. However, there were significant positive relationships between thermal heat pain threshold and LF-HRV (r = 0.47), and HF-HRV (r = 0.43) in men, but not in women. The results suggest that higher pain threshold appears to be related to greater engagement of the inhibitory parasympathetic nervous system in men only, and that other biopsychosocial mechanisms may contribute to experimental pain experience in women. Future research is needed to study these mechanisms further, accounting for other factors known to influence nociceptive and cardiovascular regulatory processes (e.g., ethnicity, hormones).
先前的研究表明,心率变异性(HRV;连续心跳之间间隔的可变性)可以预测实验性诱发疼痛的感知(即疼痛敏感性)。然而,很少有研究试图调查 HRV 与疼痛敏感性之间的性别特异性关联。这是一个重要的考虑因素,因为已经观察到静息 HRV 存在性别差异,并且对于实验性诱发疼痛的敏感性存在广泛的性别差异争论。我们研究了静息 HRV 与实验性诱发疼痛敏感性之间的关联在男性和女性中是否存在差异。共有 51 名无痛个体(26 名女性,平均年龄为 21.9 岁)参加了研究。在进行有节奏的呼吸任务期间(每分钟 15 次循环)收集静息心电图(ECG),并通过快速傅里叶变换提取 HRV 测量值。使用 Medoc 途径疼痛和感觉评估系统测量热痛觉阈值(即感觉首次被感知为疼痛而不是温暖的点)。静息 HRV 或热痛觉阈值在性别之间没有差异,性别也没有调节 HRV 与热痛觉阈值之间的关系。然而,在男性中,热痛觉阈值与 LF-HRV(r=0.47)和 HF-HRV(r=0.43)之间存在显著的正相关关系,但在女性中则没有。结果表明,较高的疼痛阈值似乎与男性中抑制性副交感神经系统的更大参与有关,而女性的实验性疼痛体验可能与其他生物心理社会机制有关。未来的研究需要进一步研究这些机制,同时考虑已知会影响伤害性和心血管调节过程的其他因素(例如,种族,激素)。