Adipose Tissue Blood Flow in Aging Humans

Sponsor
Mayo Clinic (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06096532
Collaborator
National Center for Advancing Translational Sciences (NCATS) (NIH)
24
1
2
9
2.7

Study Details

Study Description

Brief Summary

The goal of this basic science clinical trial is to understand whether adipose tissue blood flow changes between younger and older healthy adults.

The main question[s] it aims to answer are:
  • Is basal and nutrient responsive adipose tissue blood flow (ATBF) different between younger and older adults

  • What molecular and systemic signatures related to adipose tissue blood flow are altered between these two groups.

Participants will undergo measurements of adipose tissue blood flow using the xenon washout technique, undergo 2 abdominal subcutaneous adipose tissue biopsies, and drink a sugary drink.

Condition or Disease Intervention/Treatment Phase
  • Other: 75 gm oral glucose load
N/A

Detailed Description

On Visit 1, volunteers will provide written informed consent (and urine pregnancy test for women of childbearing age), complete a Dual x-ray absorptiometry scan, baseline labs (comprehensive metabolic panel) and a cardiopulmonary exercise test. Participants will arrive fasted at 08:00, and urine pregnancy test for women of childbearing age administered and an intravenous catheter will be placed. Following 30min of supine rest, baseline venous blood samples will be collected. ATBF will be assessed on participants' left abdomen first by measurement of blood flow using 133Xenon washout method. Immediately thereafter, an abdominal adipose tissue biopsy of the left side will be performed but ≥6 cm distant from location of 133Xenon injections. Subjects will them consume 75 gm glucose; because ATBF peaks 30-60 minutes following ingestion of glucose, ATBF measures will start 30 minutes after ingestion on the contralateral side followed immediately by plasma measures and another adipose tissue biopsy. During ATBF measurements, brachial blood pressure will be assessed in two-minute intervals.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Adipose Tissue Blood Flow in Aging Humans
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Older Adults

Other: 75 gm oral glucose load
Consumption of 75 gm oral glucose load in order to test nutrient responsiveness

Active Comparator: Younger Adults

Other: 75 gm oral glucose load
Consumption of 75 gm oral glucose load in order to test nutrient responsiveness

Outcome Measures

Primary Outcome Measures

  1. Adipose tissue blood flow [Baseline, pre-intervention fasting and immediately following 75 gm oral glucose load]

    blood flow will be measured in the upper body subcutaneous adipose tissue using 133 Xenon washout and reported as blood flow in ml/min/100g adipose tissue.

Secondary Outcome Measures

  1. Genomic alterations [Baseline, pre-intervention fasting and immediately following 75 gm oral glucose load]

    RNA-Seq from adipose tissue biopsies

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusion criteria

  • Within the ages of 18-35 years or 65-80 years at time of study visit

  • BMI between 20-25.0 kg/m2.

Exclusion criteria:
  • Presence of diagnosed cardiometabolic diseases (e.g., Type 2 diabetes, hypertension, Heart Failure)

  • Taking prescription anticoagulants

  • Taking prescriptions or supplements that effect adipose tissue metabolism (i.e., statins, Thiazolidinediones, niacin, atypical antipsychotics, or fish oil)

  • Pregnant or nursing

  • Inability to provide written informed consent

  • Smokers

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Minnesota Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic
  • National Center for Advancing Translational Sciences (NCATS)

Investigators

  • Principal Investigator: Kelli Lytle, PhD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Kelli A. Lytle, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT06096532
Other Study ID Numbers:
  • 23-004200
  • UL1TR002377
First Posted:
Oct 23, 2023
Last Update Posted:
Oct 23, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Oct 23, 2023