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Clinical Trials/NCT05181514
NCT05181514
Completed
Not Applicable

Impact of Plasma Lipids on β Cell Function and Insulin Sensitivity

Azienda Ospedaliero, Universitaria Pisana1 site in 1 country12 target enrollmentApril 30, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertriglyceridemia
Sponsor
Azienda Ospedaliero, Universitaria Pisana
Enrollment
12
Locations
1
Primary Endpoint
Glucose control
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The investigators aim to evaluate whether and to what extent glucose tolerance, beta cell function, insulin clearance, and glucose metabolic fluxes change in response to an acute increase in plasma triglycerides during lipid infusion, independently of free fatty acid (FFA) levels, in nondiabetic subjects.

Detailed Description

Mild hypertriglyceridemia is associated with reduced glucose tolerance and increased risk of type 2 diabetes, independent of obesity, in both cross-sectional and prospective studies. It is unclear whether this association is direct or mediated by circulating lipid substrates of triglycerides (free fatty acids, or FFA) and which are the mechanisms involved. To comprehensively examine the effects of mild acute hypertriglyceridemia on major glucose homeostatic mechanisms involved in diabetes progression, two dual-labeled oral glucose tolerance tests (OGTT) during 5-hour intravenous infusions of either 20% Intralipid or normal saline will be performed in healthy lean volunteers. Lipid-induced changes in glucose tolerance and insulin metabolism will be evaluated.

Registry
clinicaltrials.gov
Start Date
April 30, 2019
End Date
December 1, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Andrea Natali

Full Professor

Azienda Ospedaliero, Universitaria Pisana

Eligibility Criteria

Inclusion Criteria

  • age 18-65 years
  • Body mass index (BMI) 18-35 kg/m2
  • both women and men

Exclusion Criteria

  • chronic or acute diseases
  • any medications
  • pregnancy

Outcomes

Primary Outcomes

Glucose control

Time Frame: At the end of the 5-hour lipid infusion

Incremental area under the curve (AUC) of plasma glucose in response to the oral glucose tolerance test (OGTT)

Beta cell glucose sensitivity

Time Frame: At the end of the 5-hour lipid infusion

Beta cell glucose sensitivity calculated by mathematical modeling of insulin secretion rate (ISR) and plasma glucose concentrations during the oral glucose tolerance test (OGTT)

Insulin clearance

Time Frame: At the end of the 5-hour lipid infusion

Insulin clearance calculated as the ratio between insulin secretion rate (ISR) and plasma insulin levels

Rate of oral glucose appearance (RaO)

Time Frame: At the end of the 5-hour lipid infusion

The rate of oral glucose appearance (RaO) will be assessed from the time course of the plasma tracer/tracee ratio of 6,6-\[2H2\]glucose and \[U-13C\]glucose

Endogenous glucose production (EGP)

Time Frame: At the end of the 5-hour lipid infusion

The endogenous glucose production (EGP) will be assessed from the time course of the plasma tracer/tracee ratio of 6,6-\[2H2\]glucose and \[U-13C\]glucose

Insulin sensitivity

Time Frame: At the end of the 5-hour lipid infusion

Insulin sensitivity estimated by an OGTT-derived surrogate index (Matsuda index)

Insulin secretion

Time Frame: At the end of the 5-hour lipid infusion

Insulin secretion rate (ISR) estimated from C-peptide deconvolution at fasting and in response to the oral glucose tolerance test (OGTT)

Study Sites (1)

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