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临床试验/NCT06096532
NCT06096532招募中不适用

Adipose Tissue Blood Flow in Aging Humans

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2024年2月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
Mayo Clinic
入组人数
24
试验地点
1
主要终点
Adipose tissue blood flow

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Within the ages of 18-35 years or 65-80 years at time of study visit
  • BMI between 20-25.0 kg/m2.

排除标准

  • 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

研究组 & 干预措施

Older Adults

Other

干预措施: 75 gm oral glucose load (Other)

Younger Adults

Active Comparator

干预措施: 75 gm oral glucose load (Other)

结局指标

主要结局

Adipose tissue blood flow

时间窗: 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.

次要结局

  • Genomic alterations(Baseline, pre-intervention fasting and immediately following 75 gm oral glucose load)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kelli A. Lytle

Principal Investigator

Mayo Clinic

研究点 (1)

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