Pediatric Pain Research Program, Division of Hematology-Oncology, Department of Pediatrics, David Geffen School of Medicine at UCLA, 650 Charles E. Young S., #12-096 CHS, Los Angeles, CA, 90095, USA.
Division of Hematology, Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd, Mailstop #64, Los Angeles, CA, 90027, USA.
Complement Ther Med. 2020 Mar;49:102334. doi: 10.1016/j.ctim.2020.102334. Epub 2020 Feb 15.
Pain and vaso-occlusive crises (VOC) are hallmark complications of sickle cell disease (SCD) and result in significant physical and psychosocial impairment. The variability in SCD pain frequency and triggers for the transition from steady state to VOC are not well understood. This paper summarizes the harmful physiological effects of pain and emotional stressors on autonomically-mediated vascular function in individuals with SCD and the effects of a cognitive, neuromodulatory intervention (i.e. hypnosis) on microvascular blood flow. We reviewed recent studies from the authors' vascular physiology laboratory that assessed microvascular responses to laboratory stressors in individuals with SCD. Results indicate that participants with SCD exhibit marked neurally mediated vascular reactivity in response to pain, pain-related fear, and mental stress. Further, pilot study results show that engagement in hypnosis may attenuate harmful microvascular responses to pain. The collective results demonstrate that autonomically-mediated vascular responses to pain and mental stress represent an important SCD intervention target. This ongoing work provides physiological justification for the inclusion of cognitive, neuromodulatory and complementary treatments in SCD disease management and may inform the development of targeted, integrative interventions that prevent the enhancement of autonomic vascular dysfunction in SCD.
疼痛和血管阻塞性危象(VOC)是镰状细胞病(SCD)的标志性并发症,导致明显的身体和心理社会功能障碍。SCD 疼痛频率的可变性以及从稳定状态向 VOC 转变的诱因尚不清楚。本文总结了疼痛和情绪应激源对 SCD 个体自主介导的血管功能的有害生理影响,以及认知、神经调节干预(即催眠)对微血管血流的影响。我们回顾了作者血管生理学实验室的最新研究,这些研究评估了 SCD 个体对实验室应激源的微血管反应。结果表明,SCD 患者在疼痛、与疼痛相关的恐惧和精神压力下表现出明显的神经介导的血管反应性。此外,初步研究结果表明,参与催眠可能会减轻疼痛对微血管的有害反应。这些研究结果表明,自主介导的血管对疼痛和精神压力的反应是 SCD 干预的一个重要目标。这项正在进行的工作为在 SCD 疾病管理中纳入认知、神经调节和补充治疗提供了生理学依据,并可能为预防 SCD 自主血管功能障碍增强提供有针对性的综合干预措施。