Division of Extramural Research, National Center for Complementary and Integrative Health (NCCIH), National Institutes of Health (NIH), Bethesda, Maryland.
National Center for Complementary and Integrative Health (NCCIH), National Institutes of Health (NIH), Bethesda, Maryland.
J Pain. 2024 Oct;25(10):104603. doi: 10.1016/j.jpain.2024.104603. Epub 2024 Jun 13.
Sickle cell disease (SCD) is a lifelong monogenic, autosomal-recessive blood disease that predominantly affects individuals of African descent and those who self-identify as Black or Hispanic. Common SCD pathophysiological processes include adhesion, hemolysis, hypoxia, ischemia, oxidative stress, and vaso-occlusion, which often lead to substantial comorbidities and complications. Pain is one of the most common and significant clinical complications for individuals with SCD. Despite advancements in understanding the pathophysiology of SCD, the ways in which SCD pathophysiological processes contribute to nociception and pain signaling, processing, and perception remain largely unclear. Pain management for individuals with SCD is complex and presents unique challenges that must be considered depending on the presenting pain type (eg, acute pain episode vs chronic pain). Racism, stigma (including stigma associated with opioid use), and limited resources present additional challenges. Limited research has been conducted on major clinical features of SCD pain such as its ischemic, inflammatory, and neuropathic components; on its transition from acute to chronic form and across the lifespan; and on factors influencing SCD pain perception. Research on and management of SCD pain requires a whole-person approach, bringing together investigators from multiple disciplines such as hematologists, organ biologists, pain experts, physiologists, neuroscientists, psychologists, geneticists, microbiologists, immunologists, behavioral scientists, and clinicians. Multidisciplinary cross-training, with different platforms for information dissemination and communication, could help promote basic, mechanistic, and translational research to inform the optimization of current treatment strategies and the development of novel therapies for SCD pain. PERSPECTIVE: This review presents the research challenges and negative impact of SCD pain, a grossly understudied condition in a highly underserved population. It also highlights the barriers and opportunities in SCD pain research and could help clinicians better understand current treatment strategies from the whole-person perspective.
镰状细胞病(SCD)是一种终生的单基因、常染色体隐性遗传病,主要影响非洲裔人群和自认为是黑人或西班牙裔的人群。常见的 SCD 病理生理过程包括黏附、溶血、缺氧、缺血、氧化应激和血管阻塞,这些过程常常导致严重的合并症和并发症。疼痛是 SCD 患者最常见和最严重的临床并发症之一。尽管人们对 SCD 的病理生理学有了更多的了解,但 SCD 病理生理过程如何导致伤害感受和疼痛信号的传递、处理和感知,在很大程度上仍不清楚。SCD 患者的疼痛管理非常复杂,存在独特的挑战,必须根据疼痛类型(例如急性疼痛发作与慢性疼痛)来考虑。种族主义、耻辱感(包括与阿片类药物使用相关的耻辱感)和有限的资源带来了额外的挑战。对 SCD 疼痛的主要临床特征(如缺血、炎症和神经病变成分)、从急性到慢性的转变以及贯穿整个生命周期的疼痛、影响 SCD 疼痛感知的因素等方面的研究都非常有限。SCD 疼痛的研究和管理需要采用整体治疗方法,汇集血液学家、器官生物学家、疼痛专家、生理学家、神经科学家、心理学家、遗传学家、微生物学家、免疫学家、行为科学家和临床医生等多个学科的研究人员。多学科交叉培训,并建立不同的信息传播和交流平台,有助于促进基础、机制和转化研究,为优化当前的治疗策略和开发 SCD 疼痛的新疗法提供信息。观点:本文介绍了 SCD 疼痛这一严重未被研究的疾病在高度未满足需求人群中的研究挑战和负面影响。它还强调了 SCD 疼痛研究中的障碍和机遇,有助于临床医生从整体的角度更好地理解当前的治疗策略。