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Acute Effects of an Oral Fat Load on Skeletal Muscle and Hepatic Insulin Sensitivity (FLAME)

Primary Purpose

Insulin Sensitivity

Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
fat orally
Sponsored by
German Diabetes Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Insulin Sensitivity focused on measuring oral fat, insulin sensitivity

Eligibility Criteria

20 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • healthy male and female subjects
  • age 20-40
  • BMI 20-25 kg/m2

Exclusion Criteria:

  • hyperlipidemia
  • smoking
  • pregnancy
  • allergy against paracetamol/palm oil/canola oil
  • contraindication for MRI investigations
  • anaemia
  • taking drugs influencing lipid or glucose metabolism, the immune system or antihypertensive treatment
  • M. Meulengracht
  • Hepatitis/HIV
  • chronic diseases

Sites / Locations

  • German Diabetes Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Palm oil orally

Canola oil orally

Water orally

Arm Description

oral fat load

Oral fat load

oral water administration as control

Outcomes

Primary Outcome Measures

Change in rate of glucose disappearance (Rd)
Measurement of whole body insulin sensitivity in a hyperinsulinamic euglicamic clamp with deuterated glucose kinetics

Secondary Outcome Measures

Change in rate of hepatic endogenous glucose production (EGP)
Measurement of hepatic EGP in a hyperinsulinamic euglicamic clamp with deuterated glucose kinetics

Full Information

First Posted
November 26, 2012
Last Updated
August 23, 2023
Sponsor
German Diabetes Center
Collaborators
German Center for Diabetes Research
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1. Study Identification

Unique Protocol Identification Number
NCT01736202
Brief Title
Acute Effects of an Oral Fat Load on Skeletal Muscle and Hepatic Insulin Sensitivity
Acronym
FLAME
Official Title
Acute Effects of an Oral Fat Load on Skeletal Muscle and Hepatic Insulin Sensitivity (FLAME-study)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
January 1, 2022 (Actual)
Study Completion Date
January 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
German Diabetes Center
Collaborators
German Center for Diabetes Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The development of type 2 diabetes is based on a combination of insulin resistance and beta cell dysfunction. In the last years, elevated FFA were recognized as a key players in the pathogenesis of insulin resistance and type 2 diabetes. The study compares the acute effects of an oral lipid bolus on insulin sensitivity and hepatic glucose metabolism in healthy humans.
Detailed Description
A dysregulation of lipid metabolism with increased levels of free fatty acids (FFA) represents one key mechanism in the pathogenesis of insulin resistance, which contributes to the development of type 2 diabetes (T2D). In most cases, dyslipidemia is related to obesity and the metabolic syndrome. Not only skeletal muscle glucose uptake, but also hepatic glucose fluxes are altered in insulin resistant states. In obese and T2D subjects, rates of gluconeogenesis (GNG) are increased, but in obese normoglycemic subjects endogenous glucose production (EGP) remains constant because of downregulation of glycogenolysis (GL). However, in T2D subjects, both GNG and GL are elevated, contributing to fasting and postprandial hyperglycemia. Therefore, elevated GNG rates may represent an early event in the pathophysiology of insulin resistance and T2D. Preliminary studies of our institute show that intravenous lipid infusion with subsequent elevation of FFA results in increased GNG rates without alteration of EGP in lean, non-diabetic subjects. In another recent study we investigated the effects of an oral fat load on hepatic insulin sensitivity. As expected, we did not find any alterations in EGP; however, rates of GNG and GL have not been assessed. The aim of this study is to analyze the effects of an oral fat load with transiently elevated levels of circulating lipids on hepatic glucose fluxes, especially GNG and GL, to elucidate the role of dietary fat in the induction of insulin resistance in healthy humans. In this randomized, controlled cross-over study, effects of oral palm oil and canola oil ingestion will be investigated in young, healthy lean subjects. Hepatic glucose fluxes will be assessed by two independent methods, in vivo magnet resonance spectroscopy (MRS) and the deuterated water/acetaminophen method, which also allows for the determination of glycogen cycling rates. Furthermore, hepatic phosphorus metabolites and liver fat content will be monitored by MRS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Sensitivity
Keywords
oral fat, insulin sensitivity

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Palm oil orally
Arm Type
Active Comparator
Arm Description
oral fat load
Arm Title
Canola oil orally
Arm Type
Active Comparator
Arm Description
Oral fat load
Arm Title
Water orally
Arm Type
Placebo Comparator
Arm Description
oral water administration as control
Intervention Type
Biological
Intervention Name(s)
fat orally
Other Intervention Name(s)
water orally
Intervention Description
Oral ingestion of palm oil or canola oil or water at timepoint zero
Primary Outcome Measure Information:
Title
Change in rate of glucose disappearance (Rd)
Description
Measurement of whole body insulin sensitivity in a hyperinsulinamic euglicamic clamp with deuterated glucose kinetics
Time Frame
6 hours
Secondary Outcome Measure Information:
Title
Change in rate of hepatic endogenous glucose production (EGP)
Description
Measurement of hepatic EGP in a hyperinsulinamic euglicamic clamp with deuterated glucose kinetics
Time Frame
6 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy male and female subjects age 20-40 BMI 20-25 kg/m2 Exclusion Criteria: hyperlipidemia smoking pregnancy allergy against paracetamol/palm oil/canola oil contraindication for MRI investigations anaemia taking drugs influencing lipid or glucose metabolism, the immune system or antihypertensive treatment M. Meulengracht Hepatitis/HIV chronic diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Roden, Prof., MD
Organizational Affiliation
German Diabetes Center
Official's Role
Study Director
Facility Information:
Facility Name
German Diabetes Center
City
Düsseldorf
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
40225
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
34704121
Citation
Sarabhai T, Koliaki C, Mastrototaro L, Kahl S, Pesta D, Apostolopoulou M, Wolkersdorfer M, Bonner AC, Bobrov P, Markgraf DF, Herder C, Roden M. Dietary palmitate and oleate differently modulate insulin sensitivity in human skeletal muscle. Diabetologia. 2022 Feb;65(2):301-314. doi: 10.1007/s00125-021-05596-z. Epub 2021 Oct 26.
Results Reference
derived
PubMed Identifier
32434996
Citation
Sarabhai T, Kahl S, Szendroedi J, Markgraf DF, Zaharia OP, Barosa C, Herder C, Wickrath F, Bobrov P, Hwang JH, Jones JG, Roden M. Monounsaturated fat rapidly induces hepatic gluconeogenesis and whole-body insulin resistance. JCI Insight. 2020 May 21;5(10):e134520. doi: 10.1172/jci.insight.134520.
Results Reference
derived
PubMed Identifier
28112681
Citation
Hernandez EA, Kahl S, Seelig A, Begovatz P, Irmler M, Kupriyanova Y, Nowotny B, Nowotny P, Herder C, Barosa C, Carvalho F, Rozman J, Neschen S, Jones JG, Beckers J, de Angelis MH, Roden M. Acute dietary fat intake initiates alterations in energy metabolism and insulin resistance. J Clin Invest. 2017 Feb 1;127(2):695-708. doi: 10.1172/JCI89444. Epub 2017 Jan 23.
Results Reference
derived

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Acute Effects of an Oral Fat Load on Skeletal Muscle and Hepatic Insulin Sensitivity

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