BaRiatric Surgery AnD FRUctose Handeling In Obese subjecTs (BREADFRUIT)

To investigate whether changes in fructose dietary intake can help to improve dietary fructose-induced insulin resistance and post bariatric weight loss in obese subjects of Caucasian descent

Study Overview

• Status: Recruiting
• Conditions: Insulin Resistance
• Intervention / Treatment: Dietary supplement: fructose

Detailed Description

In this Randomized controlled trial, males and premenopausal women, scheduled for RYGB bariatric surgery at Spaarne Gasthuis of Caucasian Dutch descent, age ≥18 years will be put on either their high fructose diet (>100 gram fructose / day) versus a low fructose diet (<30 gram fructose intake per day isocaloric correction with dextrose) 4 weeks before bariatric surgery. For both groups, an oral (13-C labeled) fructose challenge will be performed at baseline as well as 4 weeks after start of the diet (in the week of the surgery).

Outcome measures: Primary endpoints are changes in oral fructose induced glucose and insulin postprandial plasma excursions (measured by a fructose tolerance test with 120mg 13C6-labeled fructose in relation to long term glucose handling (HOMA and Freestyle Libre) at baseline and after 4 weeks (in the week of surgery) after both diets. Secondary endpoints are changes in histology and RNA seq gene expression in liver, adipose and jejunum tissue harvested with biopsy during bariatric surgery and changes in fecal gut microbiota composition, 24h feces and urine for fructose content and (postprandial) plasma metabolites including endogenous ethanol at both timepoints. Of note, dietary intake including fructose content will be monitored by an experienced dietician from Spaarne Gasthuis. Finally, to study relations with (long term) weight loss up to 1 year after surgery related to dietary intake, the last time points at 6 and 12 months after surgery (during regular clinical outpatient visits) will be used as an exploratory endpoint to gain more insight into the relationship between gut microbiota, (pre surgery) dietary fructose intake and weight loss after bariatric surgery.

• Study Type: Interventional
• Enrollment (Anticipated): 20
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: daniko sindhunata, MD; Phone Number: 0031 20 5669111; Email: d.p.sindhunata@amsterdamumc.nl
• Study Contact Backup: Name: max nieuwdorp, MD PhD; Phone Number: 003120 5669111; Email: m.nieuwdorp@amsterdamumc.nl

Study Locations

• Netherlands
  • Amsterdam, Netherlands
    • Recruiting
    • Amsterdam UMC location AMC

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Scheduled for a RYGB gastric bypass*
• Men and premenopausal women > 18 years of age
• Caucasian descent

• Ability to provide written informed consent

  * All subjects on the waiting list meet the criteria for bariatric surgery, that is:

• BMI > 40 kg/m2 OR >35 kg/m2 with obesity related co-morbidity
• Reasonable supervised attempts to lose weight

Exclusion Criteria:

• Unstable metabolic condition defined as;

  • Diabetes with poor glycemic control (HbA1c > 8.5%);
  • Use of an antidiabetic or anti-obesity drug;
  • Malabsorptive or restrictive bariatric (weight loss) surgery in history
• Evidence for a form of liver disease (except for NAFLD without cirrhosis)
• Known genetic basis for insulin resistance or glucose intolerance
• Use of certain drugs known to produce hepatic steatosis in the previous 6 months (such as oral corticosteroids, high-dose estrogens, methotrexate, tetracycline, amiodarone)
• Malabsorptive disease orders (celiac disease, inflammatory bowel disease)
• Use of certain drugs that may injure the lining of the intestine in the previous months (colchicine, cholestyramine)
• Excessive alcohol intake (≥5 IU per day or ≥ 14 IU per week)
• Recent use of antibiotics (≤ 3 months before surgery)
• Hemostasis disorders or current treatment with anticoagulants Any primary lipid disorder
• Unable to maintain diet intervention, or unable to reliably rapport diet

Study Plan

How is the study designed?

Design Details

• Primary Purpose: BASIC_SCIENCE
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: DOUBLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
OTHER: high fructose; high fructose (>100 gram fructose / day) for 4 weeks	Dietary supplement: fructose; oral ingestion of fructose vs dextrose; Other Names: dextrose
OTHER: low fructose; low fructose diet (<30 gram fructose intake per day isocaloric correction with dextrose) for 4 weeks	Dietary supplement: fructose; oral ingestion of fructose vs dextrose; Other Names: dextrose

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
oral fructose handling	to correlate changes in oral fructose excursions (measured by AUC of fructose tolerance test enriched with 13C6-labeled fructose with glucose excursions (MAGE by Freestyle Libre)	4 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
fructose changes in visceral organs	to correlate with changes in histology and RNA seq gene expression in liver, adipose and jejunum tissue harvested with biopsy during bariatric surgery	4 weeks up to one year
gutmicrobiota	to correlate with changes in fecal gut microbiota composition	4 weeks up to one year
metabolites	to correlate with (postprandial) plasma metabolites including endogenous ethanol	4 weeks up to one year
weight	to correlate with with (long term) weight loss at 6 and 12 months after surgery	4 weeks up to one year

Collaborators and Investigators

• Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Study record dates

Study Major Dates

• Study Start (ANTICIPATED): February 5, 2023
• Primary Completion (ANTICIPATED): December 31, 2024
• Study Completion (ANTICIPATED): May 31, 2025

Study Registration Dates

• First Submitted: January 8, 2023
• First Submitted That Met QC Criteria: January 29, 2023
• First Posted (ACTUAL): February 8, 2023

Study Record Updates

• Last Update Posted (ACTUAL): February 8, 2023
• Last Update Submitted That Met QC Criteria: January 29, 2023
• Last Verified: January 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Hyperinsulinism; Insulin Resistance
• Other Study ID Numbers: 2022.0595 - NL8236601822

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: not allowed due to GDPR in Netherlands

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No