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Serum biomarkers for chronic pancreatitis pain patterns.
Saloman, Jami L; Tang, Gong; Stello, Kimberly M; Hall, Kristen E; Wang, Xianling; AlKaade, Samer; Banks, Peter A; Brand, Randall E; Conwell, Darwin L; Coté, Gregory A; Forsmark, Christopher E; Gardner, Timothy B; Gelrud, Andres; Lewis, Michele D; Sherman, Stuart; Slivka, Adam; Whitcomb, David C; Yadav, Dhiraj.
Afiliación
  • Saloman JL; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA; Pittsburgh Center for Pain Research, School of Medicine, University of Pittsburgh, PA, USA; Department of Neurobiology, School of Medicine, University of Pittsburgh,
  • Tang G; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
  • Stello KM; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA.
  • Hall KE; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA.
  • Wang X; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
  • AlKaade S; Saint Louis University, Saint Louis, MO, USA.
  • Banks PA; Brigham and Women's Hospital, Boston, MA, USA.
  • Brand RE; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA.
  • Conwell DL; The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Coté GA; Medical University of South Carolina, Charleston, SC, USA.
  • Forsmark CE; Division of Gastroenterology, Hepatology, and Nutrition, University of Florida, Gainesville, FL, USA.
  • Gardner TB; Section of Gastroenterology and Hepatology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
  • Gelrud A; Department of Internal Medicine, Miami Cancer Institute, Gastro Health, Miami, FL, USA.
  • Lewis MD; Department of Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
  • Sherman S; Indiana University School of Medicine, Indianapolis, IN, USA.
  • Slivka A; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA.
  • Whitcomb DC; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA; Pittsburgh Center for Pain Research, School of Medicine, University of Pittsburgh, PA, USA; Departments of Cell Biology & Physiology, and Human Genetics, Univers
  • Yadav D; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Pittsburgh, PA, USA.
Pancreatology ; 21(8): 1411-1418, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34602367
ABSTRACT

OBJECTIVES:

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-1ß (IL-1ß), 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Interleucina-6 / Pancreatitis Crónica Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Pancreatology Asunto de la revista: ENDOCRINOLOGIA / GASTROENTEROLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Interleucina-6 / Pancreatitis Crónica Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Pancreatology Asunto de la revista: ENDOCRINOLOGIA / GASTROENTEROLOGIA Año: 2021 Tipo del documento: Article
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