Dunbar Ellyn K, Saloman Jami L, Phillips Anna Evans, Whitcomb David C
Departments of Human Genetics and Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA.
Departments of Neurobiology and Medicine, Division of Gastroenterology, Hepatology and Nutrition, Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA, USA.
J Pain Res. 2021 Mar 17;14:773-784. doi: 10.2147/JPR.S274276. eCollection 2021.
Pain is the most distressing and disruptive feature of recurrent acute pancreatitis (RAP) and chronic pancreatitis (CP) resulting in low quality of life (QOL) and disabilities. There is no single, characteristic pain pattern in patients with RAP and CP. Abdominal imaging features of CP accurately reflect morphologic features but they do not correlate with pain. Pain is the major driver of poor quality of life (QOL) and it is the constant pain, rather than intermittent pain that drives poor QOL. Furthermore, the most severe constant pain experience in CP is also a complex condition. The ability to target the etiopathogenesis of severe pain requires new methods to detect the exact pain mechanisms in an individual at cellular, tissue, system and psychiatric levels. In patients with complex and severe disease, it is likely that multiple overlapping mechanisms are simultaneously driving pain, anxiety and depression. Quantitative sensory testing (QST) shows promise in detecting alterations in central processing of pain signals and to classify patients for mechanistic and therapeutic studies. New genetic research suggests that genetic loci for severe pain in CP overlap with genetic loci for depression and other psychiatric disorders, providing additional insights and therapeutic targets for individual patients with severe CP pain. Well-designed clinical trials that integrate clinical features, QST, genetics and psychological assessments with targeted treatment and assessment of responses are required for a quantum leap forward. A better understanding of the context and mechanisms contributing to severe pain experiences in individual patients is predicted to lead to better therapies and quality of life.
疼痛是复发性急性胰腺炎(RAP)和慢性胰腺炎(CP)最令人痛苦且具有破坏性的特征,会导致生活质量(QOL)低下和功能障碍。RAP和CP患者不存在单一的特征性疼痛模式。CP的腹部影像学特征能准确反映形态学特征,但与疼痛并无关联。疼痛是生活质量低下的主要驱动因素,导致生活质量差的是持续性疼痛,而非间歇性疼痛。此外,CP中最严重的持续性疼痛体验也是一种复杂的情况。针对严重疼痛的病因发病机制进行靶向治疗,需要新的方法在细胞、组织、系统和精神层面检测个体的确切疼痛机制。在患有复杂重症疾病的患者中,可能有多种重叠机制同时导致疼痛、焦虑和抑郁。定量感觉测试(QST)有望检测疼痛信号中枢处理的改变,并为机制和治疗研究对患者进行分类。新的基因研究表明,CP中严重疼痛的基因位点与抑郁症和其他精神障碍的基因位点重叠,为患有严重CP疼痛的个体患者提供了更多见解和治疗靶点。要实现巨大飞跃,需要精心设计的临床试验,将临床特征、QST、遗传学和心理评估与靶向治疗及反应评估相结合。预计对个体患者严重疼痛体验的背景和机制有更好的理解将带来更好的治疗方法和生活质量。