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Author Notes:

Carrie R. Daniel, Email: cdaniel@mdanderson.org

CRD designed and drafted the protocol and secured funding for the study. XZ, GB, and WS assisted with the writing and organization of the protocol manuscript. GB and WS are responsible for patient recruitment and assisted with study documentation, data collection, and the development of the manual of procedures. Study co-investigators and collaborators KBE, SMH, KLH, PCO, PS, JFP, and SK provided critical consultation on study design and laboratory tests, as well as statistical and clinical expertise. CRD is the principal investigator/chair and SK is the physician co-chair of the protocol. All authors critically reviewed and approved the content.

The authors wish to acknowledge the University of Texas MD Anderson Center’s Center for Energy Balance in Cancer Prevention and Survivorship; the Duncan Family Institute for Cancer Prevention and Risk Assessment; the Assessment, Intervention and Measurement (AIM) Core; the Bionutrition Research Core (BRC); the Kelsey Research Foundation; mentors Roberd (Robin) Bostick and Johanna Lampe; and most importantly, our participants and their families.

The authors declare that they have no competing interests. The funders did not play a role in the study design; collection and management; writing of the report; and the decision to submit the report for publication.

Subjects:

Research Funding:

The BE GONE trial is funded by the American Cancer Society (RSG-17-049-01-NEC) and the University of Texas MD Anderson Cancer Center (Institutional Research Grant) to PI: C.R. Daniel.

This study protocol has undergone peer review by the two funding bodies. X. Zhang is funded (in part) by a Research Training Award for Cancer Prevention Post-Graduate Training Program in Integrative Epidemiology from the Cancer Prevention & Research Institute of Texas, grant number RP160097 (PI: M. Spitz).

K. M. Basen-Engquist, S.M. Hanash, P.C. Okhuysen, P. Scheet, S. Kopetz, and C.R. Daniel are funded (in part) through the National Cancer Institute Cancer Center Support Grant (CCSG 5P30 CA016672–37) to MD Anderson (PI: P. Pisters).

Keywords:

  • Colorectal cancer survivors
  • Diet
  • Dry beans
  • Gut microbiome
  • Metabolome
  • Obesity
  • Precancerous colorectal polyps
  • Adult
  • Aged
  • Aged, 80 and over
  • Colonic Neoplasms
  • Colonic Polyps
  • Cross-Over Studies
  • Female
  • Gastrointestinal Microbiome
  • Humans
  • Life Style
  • Male
  • Middle Aged
  • Obesity
  • Overweight
  • Progression-Free Survival
  • Risk Factors

The BE GONE trial study protocol: A randomized crossover dietary intervention of dry beans targeting the gut microbiome of overweight and obese patients with a history of colorectal polyps or cancer

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Journal Title:

BMC Cancer

Volume:

Volume 19, Number 1

Publisher:

, Pages 1233-1233

Type of Work:

Article | Final Publisher PDF

Abstract:

Background: Mouse and human studies support the promise of dry beans to improve metabolic health and to lower cancer risk. In overweight/obese patients with a history of colorectal polyps or cancer, the Beans to Enrich the Gut microbiome vs. Obesity's Negative Effects (BE GONE) trial will test whether and how an increase in the consumption of pre-cooked, canned dry beans within the context of usual diet and lifestyle can enhance the gut landscape to improve metabolic health and reduce cancer risk. Methods/design: This randomized crossover trial is designed to characterize changes in (1) host markers spanning lipid metabolism, inflammation, and obesity-related cancer risk; (2) compositional and functional profiles of the fecal microbiome; and (3) host and microbial metabolites. With each subject serving as their own control, the trial will compare the participant's usual diet with (intervention) and without (control) dry beans. Canned, pre-cooked dry beans are provided to participants and the usual diet continually assessed and monitored. Following a 4-week run-in and equilibration period, each participant provides a total of 5 fasting blood and 6 stool samples over a total period of 16 weeks. The intervention consists of a 2-week ramp-up of dry bean intake to 1 cup/d, which is then continued for an additional 6 weeks. Intra- and inter-individual outcomes are assessed across each crossover period with consideration of the joint or modifying effects of the usual diet and baseline microbiome. Discussion: The BE GONE trial is evaluating a scalable dietary prevention strategy targeting the gut microbiome of high-risk patients to mitigate the metabolic and inflammatory effects of adiposity that influence colorectal cancer risk, recurrence, and survival. The overarching scientific goal is to further elucidate interactions between diet, the gut microbiome, and host metabolism. Improved understanding of the diet-microbiota interplay and effective means to target these relationships will be key to the future of clinical and public health approaches to cancer and other major diet- and obesity-related diseases.

Copyright information:

© The Author(s). 2019

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/rdf).
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