Severe Pain in Chronic Pancreatitis Patients: Considering Mental Health and Associated Genetic Factors

被引:20
作者
Dunbar, Ellyn K. [1 ,2 ]
Saloman, Jami L. [3 ,4 ]
Phillips, Anna Evans [2 ]
Whitcomb, David C. [4 ,5 ,6 ]
机构
[1] Univ Pittsburgh, Div Gastroenterol Hepatol & Nutr, Dept Human Genet, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Div Gastroenterol Hepatol & Nutr, Dept Med, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Dept Neurobiol, Div Gastroenterol Hepatol & Nutr, Pittsburgh Ctr Pain Res, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Dept Med, Div Gastroenterol Hepatol & Nutr, Pittsburgh Ctr Pain Res, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Dept Human Genet, Div Gastroenterol Hepatol & Nutr, Pittsburgh Ctr Pain Res, Pittsburgh, PA 15213 USA
[6] Univ Pittsburgh, Dept Cell Biol & Mol Physiol, Div Gastroenterol Hepatol & Nutr, Pittsburgh Ctr Pain Res, Pittsburgh, PA 15213 USA
关键词
pancreatitis; pain management; mental health; depression; genetic research; QUALITY-OF-LIFE; INTERNATIONAL CONSENSUS GUIDELINES; THERMAL GRILL ILLUSION; FUNCTIONAL CONNECTIVITY; PRECISION MEDICINE; WORKING GROUP; ALCOHOL; DISORDER; ANXIETY; COMORBIDITY;
D O I
10.2147/JPR.S274276
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:773 / 784
页数:12
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