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BaRiatric Surgery AnD FRUctose Handeling In Obese subjecTs (BREADFRUIT)

Primary Purpose

Insulin Resistance

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
fructose
Sponsored by
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Insulin Resistance

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Amsterdam UMC location AMCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

high fructose

low fructose

Arm Description

high fructose (>100 gram fructose / day) for 4 weeks

low fructose diet (<30 gram fructose intake per day isocaloric correction with dextrose) for 4 weeks

Outcomes

Primary Outcome Measures

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)

Secondary Outcome Measures

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
gutmicrobiota
to correlate with changes in fecal gut microbiota composition
metabolites
to correlate with (postprandial) plasma metabolites including endogenous ethanol
weight
to correlate with with (long term) weight loss at 6 and 12 months after surgery

Full Information

First Posted
January 8, 2023
Last Updated
January 29, 2023
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
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1. Study Identification

Unique Protocol Identification Number
NCT05717595
Brief Title
BaRiatric Surgery AnD FRUctose Handeling In Obese subjecTs
Acronym
BREADFRUIT
Official Title
BaRiatric Surgery AnD FRUctose Handeling In Obese subjecTs
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 5, 2023 (Anticipated)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
May 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

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
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
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized double blinded trial
Masking
ParticipantInvestigator
Masking Description
randomisation
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
high fructose
Arm Type
Other
Arm Description
high fructose (>100 gram fructose / day) for 4 weeks
Arm Title
low fructose
Arm Type
Other
Arm Description
low fructose diet (<30 gram fructose intake per day isocaloric correction with dextrose) for 4 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
fructose
Other Intervention Name(s)
dextrose
Intervention Description
oral ingestion of fructose vs dextrose
Primary Outcome Measure Information:
Title
oral fructose handling
Description
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)
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
fructose changes in visceral organs
Description
to correlate with changes in histology and RNA seq gene expression in liver, adipose and jejunum tissue harvested with biopsy during bariatric surgery
Time Frame
4 weeks up to one year
Title
gutmicrobiota
Description
to correlate with changes in fecal gut microbiota composition
Time Frame
4 weeks up to one year
Title
metabolites
Description
to correlate with (postprandial) plasma metabolites including endogenous ethanol
Time Frame
4 weeks up to one year
Title
weight
Description
to correlate with with (long term) weight loss at 6 and 12 months after surgery
Time Frame
4 weeks up to one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
daniko sindhunata, MD
Phone
0031 20 5669111
Email
d.p.sindhunata@amsterdamumc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
max nieuwdorp, MD PhD
Phone
003120 5669111
Email
m.nieuwdorp@amsterdamumc.nl
Facility Information:
Facility Name
Amsterdam UMC location AMC
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
max nieuwdorp, MD PhD
Phone
0031 20 5669111
Email
m.nieuwdorp@amsterdamumc.nl

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
not allowed due to GDPR in Netherlands

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BaRiatric Surgery AnD FRUctose Handeling In Obese subjecTs

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