Insulin resistance testing
ProcedureSteady state Plasma Glucose test
Other names: SSPG
NCT Number: NCT06657209
This study is to investigate how adipocyte (fat cell) function and fat distribution differ between individuals with normal-weight type 2 diabetes (NWD), those with overweight type 2 diabetes (OWD), and normal-weight controls without diabetes (NWC). The study will assess whether adipocyte-directed therapies, specifically pioglitazone and tirzepatide, can improve insulin resistance, adipocyte function, and fat distribution in individuals with NWD. By analyzing the biological mechanisms underlying adipocyte dysfunction, the study aims to provide insights into novel treatment strategies for improving metabolic health in normal-weight individuals with type 2 diabetes.
Interested in participating?
Request Info30 year–70 year
All sexes
Interventional
Phase 4
Stanford University, Palo Alto, California, United States
The investigators aim to learn how adipocyte dysfunction and disordered fat distribution contribute to the development of type 2 diabetes in normal-weight individuals. The investigators hope to determine whether adipocyte-directed therapies, such as pioglitazone and tirzepatide, can improve insulin sensitivity, fat distribution, and metabolic health in this population. This study is important because most diabetes research focuses on overweight or obese individuals, and very little is known about how diabetes affects those with normal body weight. Understanding the unique biology of normal-weight diabetes could lead to more personalized and effective treatment strategies, filling a gap in diabetes care for a group that can be overlooked in clinical research.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Normal-Weight Diabetes (NWD) Group:
Normal-Weight Control (NWC) Group:
Exclusion criteria
-
Steady state Plasma Glucose test
Other names: SSPG
Will collect 5 blood draws during the test to measure insulin secretion
Other names: Oral glucose tolerance test
Needle biopsy to gather a sample of abdominal subcutaneous fat
Whole body DXA scan
Abdominal MRI
Spectroscopy of the abdominal region
Other names: proton magnetic resonance spectroscopy
16 weeks started at 2.5mg/week and increased to 5mg/week dose
Other names: Mounjaro
16 weeks at a 45mg/day dose
Other names: Actos
Time frame: Baseline measures comparison between the groups
Insulin resistance will be measured by a Steady State Plasma Glucose test (SSPG). Results will be measured by glucose levels at steady state in mg/dL.
Time frame: Baseline comparisons
Adipocyte function will be measured as percent small adipocytes and peak diameter adipocytes from the fat biopsies.
Time frame: Baseline comparisons between the groups
Fat storage will be measured by MRI. Quantification of subcutaneous and visceral abdominal fat will be obtained by MRI using a fat-water imaging sequence (parameters: IDEAL-IQ: 3D GRE, 160x160 matrix, 6 echoes, 4 degree flip angle, minimum TR = 7.3 ms, 28 slices, 10 mm slice thickness.
Time frame: 16 weeks
Hemoglobin A1C measures will be compared baseline to end of 16 weeks of intervention with pioglitazone.
Time frame: 16 weeks
SSPG test results will be compared from baseline to end of pioglitazone intervention.
Results will be measured by glucose levels at steady state in mg/dL.
Time frame: Baseline comparisons between the groups
Fat storage will be measured by MRI. Quantification of subcutaneous and visceral abdominal fat will be obtained by MRI using a fat-water imaging sequence (parameters: IDEAL-IQ: 3D GRE, 160x160 matrix, 6 echoes, 4 degree flip angle, minimum TR = 7.3 ms, 28 slices, 10 mm slice thickness.
Time frame: Baseline comparisons
Adipocyte function as measured by percent small adipocytes and peak diameter adipocytes from the fat biopsies.
Time frame: Baseline measures comparison between the groups
Insulin resistance will be measured by a Steady State Plasma Glucose test (SSPG). Results will be measured by glucose levels at steady state in mg/dL.
Time frame: Baseline measured compared between the groups
A five-point, three-hour OGTT will be done after overnight fast for calculation of insulin secretion using c-peptide deconvolution, and disposition index calculated by dividing this value by SSPG.
Time frame: 16 weeks
SSPG test results will be compared from baseline to end of tirzepatide intervention. Results will be measured by glucose levels at steady state in mg/dL.
Contact information is provided by the study sponsor or research team.
Alisa Turner, BS
CONTACT
Nina Shenoy, BS
CONTACT
Stanford University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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