Harnessing Macrophage Lysosomal Lipid Metabolism in Obesity-Associated Diseases

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this study is to evaluate the role of transcription factor EB (TFEB) in adipose (fat) tissue macrophages (ATM) in regulating adipose tissue and systemic metabolic function in obesity. The investigators will assess the differences in ATM lipid metabolism in people with metabolically abnormal obesity and lean individuals. Both groups will have: * screening visit * imaging (body composition testing - dual-energy x-ray absorptiometry (DEXA) scans, magnetic resonance imaging \[MRI\] and magnetic resonance spectroscopy \[MRS\] scans) * Overnight visit with intravenous infusion (IV), muscle, and fat tissue biopsies Participants with obesity will complete meetings with study team members for a weight loss intervention to achieve a 10% body weight loss.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: t
View:

• age: ≥18 but ≤70 years

• not pregnant or breastfeeding

• weight stable and sedentary before enrollment

• no use tobacco products, excessive amounts of alcohol, or dietary supplements, or medications known to or suspected to affect glucose and lipid metabolism (aside from certain medications used to treat diabetes in the metabolically abnormal obesity \[MAO\]-Type 2 Diabetes group)

• no evidence of significant organ system dysfunction or disease (e.g. chronic severe kidney disease, cancer)

• participants must fulfil all of the following group-specific inclusion criteria below:

⁃ Lean group:

• Body mass index (BMI) ≥18.5 but \<25.0 kg/m2

• Intrahepatic triglyceride (IHTG) content \<5%

• fasting blood glucose concentration: \<100 mg/dl

• blood glucose concentration 2 h after a 75 g oral glucose challenge: \<140 mg/dl

• Hemoglobin A1C (HbA1c) \<5.7 %

⁃ Metabolically normal obesity (MNO) group:

• BMI ≥30.0 but \<45.0 kg/m2

• IHTG content \<5%

• fasting blood glucose concentration: \<100 mg/dl

• blood glucose concentration 2 h after a 75 g oral glucose challenge: \<140 mg/dl

• HbA1c \<5.7 %

⁃ Metabolically abnormal obesity (MAO)-insulin resistance and non-alcoholic fatty liver disease (NAFLD) group:

• BMI ≥30.0 but \<45.0 kg/m2

• IHTG content \>7.5%

• fasting blood glucose concentration: ≥100 but \<126 mg/dl

• blood glucose concentration 2 h after a 75 g oral glucose challenge: ≥140 but \<200 mg/dl

• HbA1c: ≥5.7 but \<6.4 %

⁃ MAO-type 2 diabetes group:

• BMI ≥30.0 but \<45.0 kg/m2

• clinical diagnosis of type 2 diabetes or fasting blood glucose concentration \>126 mg/dl or blood glucose concentration 2 h after a 75 g oral glucose challenge\>200 mg/dl or HbA1c \>6.4 % without medication if not diagnosed and medically treated for diabetes

Locations
United States
Missouri
University of Missouri School of Medicine
RECRUITING
Columbia
Contact Information
Primary
Heather McHatton
heathermchatton@health.missouri.edu
(573) 882-7619
Backup
Aman Pritish Aher
amanpritishaher@umsystem.edu
Time Frame
Start Date: 2024-08-01
Estimated Completion Date: 2028-03
Participants
Target number of participants: 60
Treatments
No_intervention: Lean Individuals
No intervention will be administered.
Experimental: Metabolically abnormal obese Individuals (obesity with normoglycemia and abnormal liver fat content)
Participants will undergo a dietary weight loss intervention to achieve 10% weight loss over about 6 months.
Experimental: Metabolically normal obese Individuals (obesity with normoglycemia and normal liver fat content)
Participants will undergo a dietary weight loss intervention to achieve 10% weight loss over about 6 months.
Experimental: Individuals with Type 2 Diabetes Mellitus
Participants will undergo a dietary weight loss intervention to achieve 10% weight loss over about 6 months.
Sponsors
Collaborators: Washington University School of Medicine, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH)
Leads: Bettina Mittendorfer

This content was sourced from clinicaltrials.gov