Insulin Sensitivity and Metabolomics During Oral Administration of Glucose and Graded Intravenous Infusion
NCT ID: NCT03223129
Last Updated: 2019-07-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
23 participants
INTERVENTIONAL
2018-01-09
2019-01-31
Brief Summary
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This project aims to study how orally ingested glucose is able to induce insulin resistance and if this response differs in patients with normal glucose tolerance, impaired glucose tolerance and in patients with type 2 diabetes mellitus. To address this question glucose homeostasis will be studied by comparing whole body glucose uptake during a progressively increased oral glucose load with a graded glucose infusion where the blood glucose levels will be kept in the same range as during the oral glucose load in patients with normal glucose tolerance, impaired glucose tolerance and patients with type 2 diabetes mellitus.
Previous studied have shown that different metabolites and bile acids could be involved the regulation of glucose homeostasis. Hence, it is possible that the gut regulates metabolites that could be involved in small intestine-induced insulin resistance described above. The aim of this research is to study metabolomics in plasma collected during the oral glucose tolerance test with increasing load of glucose and the graded glucose infusion where plasma glucose level will be held in the same levels as during the oral glucose tolerance test and study the differences in patients with normal glucose tolerance, impaired glucose tolerance and in patients with type 2 diabetes mellitus.
The expected results in this study will demonstrate that the gut plays an important role in glucose homeostasis and that this system is dysregulated in type 2 diabetes. More importantly, novel factors derived or regulated from the gut that regulate insulin resistance and glucose tolerance will be identified which could be possible targets for future antidiabetic therapies.
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Detailed Description
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Metabolomics has recently been regarded to be one of the most suitable technologies for investigating complex diseases such as type 2 diabetes mellitus because it represent a real-time functional portrait of the organisms. Previous studies have shown that different metabolites and bile acids could be involved in the regulation of glucose homeostasis. Hence it is possible that the gut regulates metabolites that could be involved in the impaired glucose tolerance and type 2 diabetes mellitus.
The specific aims of this research project are:
Aim 1: To demonstrate that orally ingested glucose induces insulin resistance and to determine if this regulation of glucose homeostasis differs between subjects with normal glucose tolerance, impaired glucose tolerance and subjects with type 2 diabetes mellitus.
Aim 2: To identify metabolites regulated by the gut that are associated with impaired glucose tolerance and type 2 diabetes mellitus.
To address this aim, differences in glucose kinetics will be studied when glucose is orally administrated (in an oral glucose tolerance test, OGTT) compared to an graded intravenous glucose infusion, were plasma glucose levels are held in the same range as during the OGTT, in subjects with normal glucose tolerance (n = 8), impaired glucose tolerance (n = 8) and type 2 diabetes mellitus (n = 8).
Basal glucose kinetics will first be assessed by double glucose tracer technique. In the basal part of the glucose tolerance tests glucose tracer nr 1 will be infused and then be followed by either a continued infusion and a gradually increasing oral glucose load (25 g, 75 g and 125 g with a 2 h interval during the OGTT) with glucose tracer nr 2 or an graded intravenous glucose tracer infusion where plasma glucose levels are adjusted to those obtained during the OGTTs.
Gas chromatography/mass spectrometry will be used to measure isotopic enrichment of glucose tracers. Insulin, glucagon, total glucagon-like peptide 1 (GLP-1) and C-peptide will be measured by radioimmunoassays repeatedly during the glucose tolerance tests. Glucose kinetics including endogenous glucose production, insulin sensitivity and insulin secretion will be calculated. Differences in glucose kinetics between the oral and intravenous administration of glucose will be calculated and compared in subjects with normal glucose tolerance, impaired glucose tolerance or type 2 diabetes mellitus.
Analysis of metabolomics will be performed in plasma collected during the OGTT and the graded intravenous glucose infusion. Metabolites in plasma samples will be analyzed using two global profiling analytical platforms and a targeted profiling platform. Two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GCxGC-TOFMS) will be performed to measure small polar metabolites. Molecular lipids will be assessed by a global platform using ultra performance liquid chromatography coupled to quadrupole-TOFMS (UPLC-QTOFMS). A targeted platform based on UPLC coupled to triple-quadrupole MS (UPLC-QqQMS) will be performed to quantify both unconjugated and conjugated forms of bile acids.
Differences in plasma metabolites during OGTT and graded intravenous glucose infusion will be studied to assess information on possible regulation by the gut and the results will be compared in subjects with normal glucose tolerance, impaired glucose tolerance and subjects with type 2 diabetes mellitus.
Significance The expected results in this study will demonstrate that the gut plays an important role in glucose homeostasis and that this system is dysregulated in type 2 diabetes. More importantly, novel factors derived or regulated from the gut that regulate insulin resistance and glucose tolerance will be identified which could be possible targets for future antidiabetic therapies.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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Patients with normal glucose tolerance
Patients included in this arm will have a plasma glucose below 140 mg/dl after a 2 h oral glucose tolerance test with a glucose load of 75 g.
All patients in this arm will undergo oral glucose tolerance test with increasing glucose load and a graded intravenous glucose infusion were plasma glucose levels are held at the same level as during the oral glucose tolerance test.
Oral glucose tolerance test
Oral glucose tolerance tests were glucose is administrated orally with an increasing load (25g, 75g, 100 g)
Graded intravenous glucose infusion
Graded intravenous glucose infusion where glucose is infused in order to receive an plasma glucose pattern comparable to those received during the oral glucose tolerance tests.
Patients with impaired glucose tolerance
Patients included in this arm will have a plasma glucose between 140 mg/dl to 199 mg/dl after a 2 h oral glucose tolerance test with a glucose load of 75 g.
All patients in this arm will undergo oral glucose tolerance test with increasing glucose load and a graded intravenous glucose infusion were plasma glucose levels are held at the same level as during the oral glucose tolerance test.
Oral glucose tolerance test
Oral glucose tolerance tests were glucose is administrated orally with an increasing load (25g, 75g, 100 g)
Graded intravenous glucose infusion
Graded intravenous glucose infusion where glucose is infused in order to receive an plasma glucose pattern comparable to those received during the oral glucose tolerance tests.
Patients with type 2 diabetes mellitus
Patients included in this arm will have a plasma glucose above 200 mg/dl after a 2 h oral glucose tolerance test with a glucose load of 75 g.
All patients in this arm will undergo oral glucose tolerance test with increasing glucose load and a graded intravenous glucose infusion were plasma glucose levels are held at the same level as during the oral glucose tolerance test.
Oral glucose tolerance test
Oral glucose tolerance tests were glucose is administrated orally with an increasing load (25g, 75g, 100 g)
Graded intravenous glucose infusion
Graded intravenous glucose infusion where glucose is infused in order to receive an plasma glucose pattern comparable to those received during the oral glucose tolerance tests.
Interventions
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Oral glucose tolerance test
Oral glucose tolerance tests were glucose is administrated orally with an increasing load (25g, 75g, 100 g)
Graded intravenous glucose infusion
Graded intravenous glucose infusion where glucose is infused in order to receive an plasma glucose pattern comparable to those received during the oral glucose tolerance tests.
Eligibility Criteria
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Inclusion Criteria
* BMI between 35 and 60 kg/m2
* Ability to understand and comply with the study process.
Exclusion Criteria
* Previous bariatric surgery;
* History of medical problems such as mental impairment;
* Major cardiovascular disease;
* Major gastrointestinal disease;
* Major respiratory disease;
* Hormonal disorders;
* Infection;
* History of drug addiction and/or alcohol abuse;
* Internal malignancy;
* Pregnancy;
* Suspected or confirmed poor compliance;
20 Years
65 Years
ALL
No
Sponsors
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Steno Diabetes Center Copenhagen
OTHER
Catholic University of the Sacred Heart
OTHER
Responsible Party
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Geltrude Mingrone
Professor
Principal Investigators
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Geltrude Mingrone, MD PhD
Role: PRINCIPAL_INVESTIGATOR
The Catholic University of the Sacred Heart
Locations
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Università Cattolica S. Cuore
Roma, , Italy
Countries
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References
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Mingrone G, Panunzi S, De Gaetano A, Ahlin S, Spuntarelli V, Bondia-Pons I, Barbieri C, Capristo E, Gastaldelli A, Nolan JJ. Insulin sensitivity depends on the route of glucose administration. Diabetologia. 2020 Jul;63(7):1382-1395. doi: 10.1007/s00125-020-05157-w. Epub 2020 May 8.
Other Identifiers
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U911/14
Identifier Type: -
Identifier Source: org_study_id
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