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Dietary Green Tea Confection For Resolving Gut Permeability-Induced Metabolic Endotoxemia In Obese Adults

Primary Purpose

Obesity, Endotoxemia, Inflammation

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Green Tea Extract
Placebo
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Overweight/obese (BMI = 28-40 kg/m2)
  • Fasting glucose < 126 mg/dL
  • Normotensive (blood pressure < 140/90 mmHg)
  • Non-dietary supplement user
  • Non-smoker

Exclusion Criteria:

  • Regular tea drinkers (> 2 cups/week)
  • Vegetarians
  • Use of medications to manage diabetes, hypertension, or hyperlipidemia
  • Use of any medications known to be contraindicated for use with green tea ingestion
  • User of dietary supplements, prebiotics, or probiotics
  • Recent use of antibiotics or anti-inflammatory agents
  • Women who are pregnant or lactating or have initiated or changed birth control in the past 3-months
  • Individuals with gastrointestinal disorders or surgeries
  • Individuals with hemochromatosis
  • Alcohol intake > 3 drinks per day
  • Any history of cancer

Sites / Locations

  • Ohio State University

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo Confection

Green Tea Extract-Confection

Arm Description

Confection without green tea extract consumed daily for 4 weeks

Confection with green tea extract consumed daily for 4 weeks

Outcomes

Primary Outcome Measures

Endotoxin
Serum endotoxin concentration
Endotoxin
Serum endotoxin concentration
Endotoxin
Serum endotoxin concentration

Secondary Outcome Measures

Gut Permeability - Lactulose to Mannitol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Lactulose to Mannitol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Lactulose to Mannitol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Lactulose to Mannitol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Sucralose to Erythritol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Sucralose to Erythritol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Sucralose to Erythritol Ratio
Ratio of excretion of urinary sugars
Gut Permeability - Sucralose to Erythritol Ratio
Ratio of excretion of urinary sugars
Firmicutes to Bacteroidetes Ratio - Microbiota
Ratio of relative abundances of Firmicutes to Bacteroidetes in feces
Firmicutes to Bacteroidetes Ratio - Microbiota
Ratio of relative abundances of Firmicutes to Bacteroidetes in feces
Bioavailability - Epigallocatechin gallate
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Bioavailability - Epigallocatechin
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Bioavailability - Epicatechin gallate
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Bioavailability - Epicatechin
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Cmax of Epigallocatechin gallate
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Cmax of Epigallocatechin
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Cmax of Epicatechin gallate
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Cmax of Epicatechin
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Tmax of Epigallocatechin gallate
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Tmax of Epigallocatechin
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Tmax of Epicatechin gallate
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Tmax of Epicatechin
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Calprotectin
Fecal calprotectin concentration
Calprotectin
Fecal calprotectin concentration

Full Information

First Posted
January 22, 2018
Last Updated
December 4, 2021
Sponsor
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT03413735
Brief Title
Dietary Green Tea Confection For Resolving Gut Permeability-Induced Metabolic Endotoxemia In Obese Adults
Official Title
Dietary Green Tea Confection For Resolving Gut Permeability-Induced Metabolic Endotoxemia In Obese Adults
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 29, 2018 (Actual)
Primary Completion Date
March 30, 2022 (Anticipated)
Study Completion Date
March 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is focused on assessing gastrointestinal-level improvements by which green tea limits metabolic endotoxemia. It is expected that catechin-rich green tea will improve gut barrier function to prevent endotoxin translocation and associated low-grade inflammation. Outcomes will therefore support dietary recommendations for green tea to alleviate obesity-related inflammatory responses. Specifically, the study is expected to demonstrate that a green tea confection snack food can attenuate metabolic endotoxemia in association with restoring gastrointestinal health.
Detailed Description
Obesity is a major public health concern in the United States, with over two-thirds of the adult population classified as overweight or obese. Obesity is characterized by low-grade chronic inflammation that, in part, is mediated by metabolic endotoxemia. Metabolic endotoxemia describes increased circulating levels of gut-derived endotoxin (a bacterial product derived from Gram-negative bacteria in the intestines) that results from gut barrier dysfunction, a phenomenon that is common in obesity. Studies in rodents models have shown that dietary supplementation with green tea extract (GTE) reduces metabolic endotoxemia in association with improved gut health. This clinical trial will therefore investigate the extent to which a green tea confection snack food can alleviate metabolic endotoxemia and restore gut health in obese humans. It is hypothesized that 4-week daily ingestion of a green tea extract (GTE)-rich confection will limit metabolic endotoxemia by decreasing gut barrier permeability. This study will address the following objectives: 1) define alterations in catechin pharmacokinetics in obese compared with healthy adults, 2) demonstrate improvements in gut barrier function by GTE, and 3) demonstrate GTE-mediated amelioration of microbial dysbiosis. To test the hypothesis, all participants will complete a 12-h pharmacokinetics study to define the influence of obesity on catechin bioavailability and metabolism. They will then complete a double-blind, randomized, placebo-controlled trial where they will receive a GTE-rich or placebo confection for 4 weeks. Prior to and upon completing the intervention, participants will undergo a gut permeability test, fecal samples will be collected for microbiota composition analysis, and blood samples will be collected to assess endotoxin and inflammatory biomarkers. Upon successfully completing this study, it is anticipated that chronic consumption of a green tea confection will be demonstrated to be an effective dietary strategy to reduce metabolic endotoxemia and improve gut health.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Endotoxemia, Inflammation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo Confection
Arm Type
Placebo Comparator
Arm Description
Confection without green tea extract consumed daily for 4 weeks
Arm Title
Green Tea Extract-Confection
Arm Type
Experimental
Arm Description
Confection with green tea extract consumed daily for 4 weeks
Intervention Type
Other
Intervention Name(s)
Green Tea Extract
Intervention Description
Confections containing green tea extract that will be ingested daily for 4 weeks
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Confections containing no green tea extract that will be ingested daily for 4 weeks
Primary Outcome Measure Information:
Title
Endotoxin
Description
Serum endotoxin concentration
Time Frame
Week 0 - Fasting
Title
Endotoxin
Description
Serum endotoxin concentration
Time Frame
Week 2 - Fasting
Title
Endotoxin
Description
Serum endotoxin concentration
Time Frame
Week 4 - Fasting
Secondary Outcome Measure Information:
Title
Gut Permeability - Lactulose to Mannitol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 0 - 0-5 hours
Title
Gut Permeability - Lactulose to Mannitol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 0 - 6-24 hours
Title
Gut Permeability - Lactulose to Mannitol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 4 - 0-5 hours
Title
Gut Permeability - Lactulose to Mannitol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 4 - 6-24 hours
Title
Gut Permeability - Sucralose to Erythritol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 0 - 0-5 hours
Title
Gut Permeability - Sucralose to Erythritol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 0 - 6-24 hours
Title
Gut Permeability - Sucralose to Erythritol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 4 - 0-5 hours
Title
Gut Permeability - Sucralose to Erythritol Ratio
Description
Ratio of excretion of urinary sugars
Time Frame
Week 4 - 6-24 hours
Title
Firmicutes to Bacteroidetes Ratio - Microbiota
Description
Ratio of relative abundances of Firmicutes to Bacteroidetes in feces
Time Frame
Week 0
Title
Firmicutes to Bacteroidetes Ratio - Microbiota
Description
Ratio of relative abundances of Firmicutes to Bacteroidetes in feces
Time Frame
Week 4
Title
Bioavailability - Epigallocatechin gallate
Description
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of a green tea confection
Title
Bioavailability - Epigallocatechin
Description
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of a green tea confection
Title
Bioavailability - Epicatechin gallate
Description
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of a green tea confection
Title
Bioavailability - Epicatechin
Description
Area under the curve (AUC) of plasma catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of a green tea confection
Title
Cmax of Epigallocatechin gallate
Description
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Cmax of Epigallocatechin
Description
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Cmax of Epicatechin gallate
Description
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Cmax of Epicatechin
Description
Maximum plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Tmax of Epigallocatechin gallate
Description
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Tmax of Epigallocatechin
Description
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Tmax of Epicatechin gallate
Description
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Tmax of Epicatechin
Description
Time to maximal plasma concentration of catechins calculated from blood collected at 0, 0.25, 0.5, 1, 2, 3, 5, 8, 10, 12 hours post-ingestion of green tea confection
Time Frame
0-12 hours post-ingestion of green tea confection
Title
Calprotectin
Description
Fecal calprotectin concentration
Time Frame
Week 0
Title
Calprotectin
Description
Fecal calprotectin concentration
Time Frame
Week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Overweight/obese (BMI = 28-40 kg/m2) Fasting glucose < 126 mg/dL Normotensive (blood pressure < 140/90 mmHg) Non-dietary supplement user Non-smoker Exclusion Criteria: Regular tea drinkers (> 2 cups/week) Vegetarians Use of medications to manage diabetes, hypertension, or hyperlipidemia Use of any medications known to be contraindicated for use with green tea ingestion User of dietary supplements, prebiotics, or probiotics Recent use of antibiotics or anti-inflammatory agents Women who are pregnant or lactating or have initiated or changed birth control in the past 3-months Individuals with gastrointestinal disorders or surgeries Individuals with hemochromatosis Alcohol intake > 3 drinks per day Any history of cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Bruno, PhD, RD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data will be published as aggregate only. Data sharing may be possible pending institutional agreements.
Citations:
PubMed Identifier
28038359
Citation
Li J, Sapper TN, Mah E, Moller MV, Kim JB, Chitchumroonchokchai C, McDonald JD, Bruno RS. Green tea extract treatment reduces NFkappaB activation in mice with diet-induced nonalcoholic steatohepatitis by lowering TNFR1 and TLR4 expression and ligand availability. J Nutr Biochem. 2017 Mar;41:34-41. doi: 10.1016/j.jnutbio.2016.12.007. Epub 2016 Dec 21.
Results Reference
background
PubMed Identifier
29190550
Citation
Li J, Sasaki GY, Dey P, Chitchumroonchokchai C, Labyk AN, McDonald JD, Kim JB, Bruno RS. Green tea extract protects against hepatic NFkappaB activation along the gut-liver axis in diet-induced obese mice with nonalcoholic steatohepatitis by reducing endotoxin and TLR4/MyD88 signaling. J Nutr Biochem. 2018 Mar;53:58-65. doi: 10.1016/j.jnutbio.2017.10.016. Epub 2017 Nov 3.
Results Reference
background

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Dietary Green Tea Confection For Resolving Gut Permeability-Induced Metabolic Endotoxemia In Obese Adults

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