Reduction of inflammation in chronic pancreatitis using a soy bread intervention: A feasibility study

Jennifer Ahn-Jarvis, Erin Lombardo, Zobeida Cruz-Monserrate, Niharika Badi, Olivia Crowe, Sabrina Kaul, Hannah Komar, Somashekar G. Krishna, Gregory B. Lesinski, Thomas A. Mace, Mitchell L. Ramsey, Kristen Roberts, Kyle Stinehart, Madelyn Traczek, Darwin L. Conwell, Yael Vodovotz, Phil A. Hart

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Introduction: Chronic pancreatitis is a chronic inflammatory disease, which progresses to fibrosis. Currently there are no interventions to delay or stop the progression to irreversible organ damage. In this study, we assessed the tolerability and feasibility of administering soy bread to reduce circulating inflammatory mediators. Methods: Subjects with chronic pancreatitis diagnosed using the American Pancreatic Association diagnostic guidelines were enrolled. During the dose escalation (DE) phase, subjects received one week of soy bread based using a 3 + 3 dose-escalation design, which was then followed by a maximally tolerated dose (MTD) phase with four weeks of intervention. Dose-limiting toxicities (DLTs) were monitored. Plasma cytokine levels were measured using a Meso Scale Discovery multiplex assay kit. Isoflavonoid excretion in 24-h urine collection was used to measure soy bread compliance. Results: Nine subjects completed the DE phase, and one subject completed the MTD phase without any DLTs at a maximum dosage of three slices (99 mg of isoflavones) per day. Reported compliance to soy bread intervention was 98%, and this was confirmed with urinary isoflavones and their metabolites detected in all subjects. There was a significant decline in the TNF-α level during the DE phase (2.667 vs 2.382 pg/mL, p = 0.039); other levels were similar. Conclusions: In this feasibility study, there was excellent compliance with a short-term intervention using soy bread in chronic pancreatitis. Reduction was seen in at least one pro-inflammatory cytokine with short-term intervention. Larger cohorts and longer interventions with soy are warranted to assess the efficacy of reducing pro-inflammatory mediators of disease.

Original languageEnglish
Pages (from-to)852-859
Number of pages8
JournalPancreatology
Volume20
Issue number5
DOIs
StatePublished - Jul 2020

Bibliographical note

Publisher Copyright:
© 2020 IAP and EPC

Funding

This study was funded by a pilot grant from the American College of Gastroenterology. Research reported in this publication was also supported by the National Cancer Institute and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) under award number U01DK108327 (ZCM, DC and PH). The project described was also supported by Award Number Grant UL1TR002733 from the National Center For Advancing Translational Sciences. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. This study was funded by a pilot grant from the American College of Gastroenterology . Research reported in this publication was also supported by the National Cancer Institute and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) under award number U01DK108327 (ZCM, DC and PH). The project described was also supported by Award Number Grant UL1TR002733 from the National Center For Advancing Translational Sciences . The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

FundersFunder number
National Institutes of Health (NIH)
National Childhood Cancer Registry – National Cancer Institute
National Institute of Diabetes and Digestive and Kidney DiseasesU01DK108327
National Center for Advancing Translational Sciences (NCATS)UL1TR002733
American College of Gastroenterology

    Keywords

    • Feasibility study
    • IL-6
    • Isoflavones
    • Soy bread
    • TNF-Alpha

    ASJC Scopus subject areas

    • Endocrinology
    • Endocrinology, Diabetes and Metabolism
    • Hepatology

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