NCT02994459

Brief Summary

People who are obese often have insulin resistance (inability of insulin to properly control blood sugar) and high blood sugar. However, not all people with obesity have this problem. About one-third of people with obesity have normal sugar metabolism (the way your body uses sugar). Similarly, not all people who are lean are also metabolically healthy and a subset of people who are lean are referred to as metabolically abnormal lean (MAL) or metabolically obese lean because they have the abnormalities in glucose metabolism typically associated with obesity. The reasons why some people with obesity have a problem with blood sugar control and others do not are not entirely clear. It is thought that impaired muscle sugar uptake is the main problem related to high blood sugar in people with obesity. However, adipose tissue (fat tissue) also consumes a substantial amount of blood sugar. Therefore, it is unclear whether muscle or adipose tissue (fat tissue) are primarily responsible for altered blood sugar concentrations in persons with metabolically abnormal obesity (MAO) (those with insulin resistance), compared to those with metabolically normal (healthy) obesity (MNO), or whether "healthy" adipose tissue (fat tissue) expansion in MNO people compared with lean people provides a vessel for blood sugar removal that helps maintain normal blood sugar concentration. Accordingly, the investigators will determine the amount of sugar that is taken up by the body and in the cells of adipose tissue (fat tissue) and muscle by infusing labeled sugar into the blood and looking at its disappearance from blood and appearance in adipose tissue (fat tissue) and muscle. The investigators will also determine how well insulin, a hormone that controls blood sugar, turns on signals that stimulate sugar uptake in fat and muscle cells. These studies will be done after an overnight fast and during an infusion of sugar and insulin (hyperinsulinemic-euglycemic clamp), in sex- and age-matched people who are insulin resistant and insulin sensitive. People with obesity will also be invited to complete a \~10% diet-induced weight loss program and will be studied again after they have achieved the weight loss goal. A group of sex- and age-matched metabolically normal lean participants will serve as control group. An attempt will be made to also study a group of sex- and age-matched metabolically abnormal lean participants.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for all trials

Timeline
8mo left

Started Jul 2017

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress93%
Jul 2017Jan 2027

First Submitted

Initial submission to the registry

December 9, 2016

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 15, 2016

Completed
7 months until next milestone

Study Start

First participant enrolled

July 1, 2017

Completed
9.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2027

Last Updated

March 17, 2025

Status Verified

March 1, 2025

Enrollment Period

9.5 years

First QC Date

December 9, 2016

Last Update Submit

March 14, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Contribution of subcutaneous adipose tissue glucose uptake to whole-body glucose disposal in people who are insulin sensitive or insulin resistant (defined as insulin-mediated glucose disposal rate)

    Comparison of whole body and total adipose tissue glucose disposal rate assessed by using stable isotope labeled glucose tracer infusion in conjunction with dynamic PET imaging

    Baseline

Study Arms (4)

Metabolically Normal Obese (likely insulin sensitive)

i) BMI ≥30.0 but \<45.0 kg/m2; maximum body circumference \<165 cm to ensure subjects fit into the PET/CT and MR scanners; iii) fasting blood glucose: \<100 mg/dl; iv) blood glucose 2 h after an OGTT: \<140 mg/dl; v) HbA1c \<5.7 %; vi) fasting insulin: \<20 µU/mL.

Other: Weight Loss

Metabolically Abnormal Obese (likely insulin resistant)

i) BMI ≥30.0 but \<45.0 kg/m2; maximum body circumference \<165 cm to ensure subjects fit into the PET/CT and MR scanners; iii) fasting blood glucose: ≥100 mg/dl or blood glucose 2 h after an OGTT: ≥140 or fasting insulin: \>20 µU/mL.

Other: Weight Loss

Metabolically Normal Lean

i) BMI ≥18.5 but \<25.0 kg/m2; ii) maximum body circumference \<165 cm to ensure subjects fit into the PET/CT and MR scanners; iii) fasting blood glucose: \<100 mg/dl; iv) blood glucose 2 h after an OGTT: \<140 mg/dl; v) HbA1c \<5.7 %; vi) fasting insulin: \<20 µU/mL.

Metabolically Abnormal Lean

i) BMI ≥18.5 but \<25.0 kg/m2; ii) maximum body circumference \<165 cm to ensure subjects fit into the PET/CT and MR scanners; iii) iii) fasting blood glucose: ≥100 mg/dl or blood glucose 2 h after an OGTT: ≥140 or fasting insulin: \>20 µU/mL.

Interventions

Diet-induced weight loss (obese only)

Metabolically Abnormal Obese (likely insulin resistant)Metabolically Normal Obese (likely insulin sensitive)

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

The investigators plan to study a total of 45 men and women of all races and ethnic groups: 15 MAO (metabolically abnormal obese, likely insulin resistant), 15 MNO (metabolically normal obese, likely insulin sensitive), and 15 lean. All three groups will be balanced with regards to sex and race/ethnicity distribution, and the two obese groups will also be matched on percent total body fat. They will also attempt to recruit 15 metabolically abnormal lean participants.

You may qualify if:

  • All subjects
  • Age: greater than or equal to 18 years but \<65 years
  • Weight stable (i.e., ±2 kg for at least 3 months)
  • Sedentary (less than 1 hour of structured exercise per week)
  • No evidence of significant organ system dysfunction or disease (e.g., diabetes, impaired kidney function, cancer, etc.)
  • Metabolically Normal Lean
  • BMI greater than or equal to 18.5 but \<25.0 kg/m2
  • Fasting blood glucose: \<100 mg/dl
  • Blood glucose 2 h after an OGTT: \<140 mg/dl
  • HbA1c \<5.7 %.
  • Metabolically Normal Obese, likely insulin sensitive
  • BMI greater than or equal to 30.0 but \<45.0 kg/m2
  • Fasting blood glucose: \<100 mg/dl
  • Fasting insulin: \<20 mU/l
  • Blood glucose 2 h after an OGTT: \<140 mg/dl
  • +7 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Washington University School of Medicine

St Louis, Missouri, 63110, United States

Location

Related Publications (2)

  • Cao C, Koh HE, Van Vliet S, Patterson BW, Reeds DN, Laforest R, Gropler RJ, Mittendorfer B. Increased plasma fatty acid clearance, not fatty acid concentration, is associated with muscle insulin resistance in people with obesity. Metabolism. 2022 Jul;132:155216. doi: 10.1016/j.metabol.2022.155216. Epub 2022 May 13.

  • van Vliet S, Koh HE, Patterson BW, Yoshino M, LaForest R, Gropler RJ, Klein S, Mittendorfer B. Obesity Is Associated With Increased Basal and Postprandial beta-Cell Insulin Secretion Even in the Absence of Insulin Resistance. Diabetes. 2020 Oct;69(10):2112-2119. doi: 10.2337/db20-0377. Epub 2020 Jul 10.

Biospecimen

Retention: SAMPLES WITH DNA

Blood and adipose/muscle tissue samples

MeSH Terms

Conditions

Glucose Metabolism Disorders

Condition Hierarchy (Ancestors)

Metabolic DiseasesNutritional and Metabolic Diseases

Study Officials

  • Bettina Mittendorfer, PhD

    Washington University School of Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior Associate Dean for Research; Professor, Medicine & Nutrition; NextGen Director of Clinical and Translational Sciences Unit

Study Record Dates

First Submitted

December 9, 2016

First Posted

December 15, 2016

Study Start

July 1, 2017

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

January 1, 2027

Last Updated

March 17, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will share

The investigators do not currently anticipate to share IPD, but will do so upon request.

Locations