Serum biomarkers for chronic pancreatitis pain patterns

dc.contributor.authorSaloman, Jami L.
dc.contributor.authorTang, Gong
dc.contributor.authorStello, Kimberly M.
dc.contributor.authorHall, Kristen E.
dc.contributor.authorWang, Xianling
dc.contributor.authorAlKaade, Samer
dc.contributor.authorBanks, Peter A.
dc.contributor.authorBrand, Randall E.
dc.contributor.authorConwell, Darwin L.
dc.contributor.authorCoté, Gregory A.
dc.contributor.authorForsmark, Christopher E.
dc.contributor.authorGardner, Timothy B.
dc.contributor.authorGelrud, Andres
dc.contributor.authorLewis, Michele D.
dc.contributor.authorSherman, Stuart
dc.contributor.authorSlivka, Adam
dc.contributor.authorWhitcomb, David C.
dc.contributor.authorYadav, Dhiraj
dc.contributor.authorNAPS consortium
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2023-10-12T11:37:52Z
dc.date.available2023-10-12T11:37:52Z
dc.date.issued2021
dc.description.abstractObjectives: Chronic pancreatitis (CP) is associated with debilitating refractory pain. Distinct subtypes of CP pain have been previously characterized based on severity (none, mild-moderate, severe) and temporal (none, intermittent, constant) nature of pain, but no mechanism-based tools are available to guide pain management. This exploratory study was designed to determine if potential pain biomarkers could be detected in patient serum and whether they associate with specific pain patterns. Methods: Cytokines, chemokines, and peptides associated with nociception and pain were measured in legacy serum samples from CP patients (N = 99) enrolled in the North American Pancreatitis Studies. The unsupervised hierarchical cluster analysis was applied to cluster CP patients based on their biomarker profile. Classification and regression tree was used to assess whether these biomarkers can predict pain outcomes. Results: The hierarchical cluster analysis revealed a subset of patients with predominantly constant, mild-moderate pain exhibited elevated interleukin-1β (IL-1β), interleukin-6 (IL-6), interleukin-2 (IL-2), tumor necrosis factor alpha (TNFα), and monocyte chemoattractant protein-1 (MCP1) whereas patients with higher interleukin-4 (IL-4), interleukin-8 (IL-8) and calcitonin gene related peptide (CGRP) were more likely to have severe pain. Interestingly, analyses of each individual biomarker revealed that patients with constant pain had reduced circulating TNFα and fractalkine. Patients with severe pain exhibited a significant reduction in TNFα as well as trends towards lower levels of IL-6 and substance P. Discussion: The observations from this study indicate that unique pain experiences within the chronic pancreatitis population can be associated with distinct biochemical signatures. These data indicate that further hypothesis-driven analyses combining biochemical measurements and detailed pain phenotyping could be used to develop precision approaches for pain management in patients with chronic pancreatitis.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationSaloman JL, Tang G, Stello KM, et al. Serum biomarkers for chronic pancreatitis pain patterns. Pancreatology. 2021;21(8):1411-1418. doi:10.1016/j.pan.2021.09.016
dc.identifier.urihttps://hdl.handle.net/1805/36297
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.pan.2021.09.016
dc.relation.journalPancreatology
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectPain biomarkers
dc.subjectSerum
dc.subjectChronic pancreatitis
dc.subjectPain severity
dc.subjectPain frequency
dc.titleSerum biomarkers for chronic pancreatitis pain patterns
dc.typeArticle
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