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Impact of Plasma Lipids on β Cell Function and Insulin Sensitivity

Primary Purpose

Hypertriglyceridemia, Glucose Intolerance

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
20% Intralipid
Normal Saline
Sponsored by
Azienda Ospedaliero, Universitaria Pisana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Hypertriglyceridemia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Azienda Ospedaliero-Universitaria Pisana

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Normal Saline

20% Intralipid

Arm Description

Participants will undergo a dual labeled, 3-h oral glucose tolerance test (OGTT) during i.v. infusion of normal saline

Participants will undergo a dual labeled, 3-h oral glucose tolerance test (OGTT) during i.v. infusion of Intralipid 20%.

Outcomes

Primary Outcome Measures

Glucose control
Incremental area under the curve (AUC) of plasma glucose in response to the oral glucose tolerance test (OGTT)
Insulin secretion
Insulin secretion rate (ISR) estimated from C-peptide deconvolution at fasting and in response to the oral glucose tolerance test (OGTT)
Beta cell glucose sensitivity
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 sensitivity
Insulin sensitivity estimated by an OGTT-derived surrogate index (Matsuda index)
Insulin clearance
Insulin clearance calculated as the ratio between insulin secretion rate (ISR) and plasma insulin levels
Rate of oral glucose appearance (RaO)
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)
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

Secondary Outcome Measures

Full Information

First Posted
December 6, 2021
Last Updated
January 4, 2022
Sponsor
Azienda Ospedaliero, Universitaria Pisana
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1. Study Identification

Unique Protocol Identification Number
NCT05181514
Brief Title
Impact of Plasma Lipids on β Cell Function and Insulin Sensitivity
Official Title
Impact of Plasma Lipids on β Cell Function and Insulin Sensitivity
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
April 30, 2019 (Actual)
Primary Completion Date
December 1, 2021 (Actual)
Study Completion Date
December 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliero, Universitaria Pisana

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertriglyceridemia, Glucose Intolerance

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Normal Saline
Arm Type
Placebo Comparator
Arm Description
Participants will undergo a dual labeled, 3-h oral glucose tolerance test (OGTT) during i.v. infusion of normal saline
Arm Title
20% Intralipid
Arm Type
Experimental
Arm Description
Participants will undergo a dual labeled, 3-h oral glucose tolerance test (OGTT) during i.v. infusion of Intralipid 20%.
Intervention Type
Other
Intervention Name(s)
20% Intralipid
Intervention Description
Participants will receive a 5 h primed (375 mL/m2)-continuous (25 mL h-1 m-2) i.v. infusion of 20% fat emulsion (Intralipid 20%), together with a 5 h primed (28 µmol/kg)-continuous (0.28 µmol min-1 kg-1) infusion of 6,6-[2H2]glucose. After 2 h, participants will consume within 5 min an oral glucose drink consisting of 147 mL of 50% dextrose solution (wt/vol) enriched with 1.5 g of [U-13C] glucose.
Intervention Type
Other
Intervention Name(s)
Normal Saline
Intervention Description
Participants will receive a 5 h primed (375 mL/m2)-continuous (25 mL h-1 m-2) i.v. infusion of normal saline (Sodium Chloride 0.9%), together with a 5 h primed (28 µmol/kg)-continuous (0.28 µmol min-1 kg-1) infusion of 6,6-[2H2]glucose. After 2 h, participants will consume within 5 min an oral glucose drink consisting of 147 mL of 50% dextrose solution (wt/vol) enriched with 1.5 g of [U-13C] glucose.
Primary Outcome Measure Information:
Title
Glucose control
Description
Incremental area under the curve (AUC) of plasma glucose in response to the oral glucose tolerance test (OGTT)
Time Frame
At the end of the 5-hour lipid infusion
Title
Insulin secretion
Description
Insulin secretion rate (ISR) estimated from C-peptide deconvolution at fasting and in response to the oral glucose tolerance test (OGTT)
Time Frame
At the end of the 5-hour lipid infusion
Title
Beta cell glucose sensitivity
Description
Beta cell glucose sensitivity calculated by mathematical modeling of insulin secretion rate (ISR) and plasma glucose concentrations during the oral glucose tolerance test (OGTT)
Time Frame
At the end of the 5-hour lipid infusion
Title
Insulin sensitivity
Description
Insulin sensitivity estimated by an OGTT-derived surrogate index (Matsuda index)
Time Frame
At the end of the 5-hour lipid infusion
Title
Insulin clearance
Description
Insulin clearance calculated as the ratio between insulin secretion rate (ISR) and plasma insulin levels
Time Frame
At the end of the 5-hour lipid infusion
Title
Rate of oral glucose appearance (RaO)
Description
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
Time Frame
At the end of the 5-hour lipid infusion
Title
Endogenous glucose production (EGP)
Description
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
Time Frame
At the end of the 5-hour lipid infusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Natali, MD
Organizational Affiliation
University of Pisa
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliero-Universitaria Pisana
City
Pisa
State/Province
PI
ZIP/Postal Code
56127
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact of Plasma Lipids on β Cell Function and Insulin Sensitivity

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