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临床试验/NCT06571474
NCT06571474招募中不适用

Harnessing Macrophage Lysosomal Lipid Metabolism in Obesity-Associated Diseases

Bettina Mittendorfer1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
24-hour plasma glucose concentration

研究概览

简要总结

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

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •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

排除标准

  • •- Individuals that do not meet all inclusion Criterion

研究组 & 干预措施

Lean Individuals

No intervention will be administered.

Metabolically abnormal obese Individuals

Obesity with normoglycemia and abnormal liver fat content

Metabolically normal obese Individuals

Obesity with normoglycemia and normal liver fat content

Individuals with Type 2 Diabetes Mellitus

Pre-Diagnosed type 2 diabetics

结局指标

主要结局

24-hour plasma glucose concentration

时间窗: Within 2 weeks of Clinical Visit

Insulin sensitivity

时间窗: Within 2 weeks of Clinical Visit

Sensitivity assessed as insulin-mediated glucose disposal during a hyperinsulinemic-euglycemic clamp procedure

Macrophage isolation in adipose tissue biopsy

时间窗: Within 2 weeks of Clinical Visit

macrophage gene expression using RNA sequencing and fluorescent activated cell sorting (FACS)

Macrophage isolation in skeletal muscle tissue

时间窗: Within 2 weeks of Clinical Visit

macrophage gene expression using RNA sequencing and fluorescent activated cell sorting (FACS)

次要结局

未报告次要终点

研究者

发起方
Bettina Mittendorfer
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Bettina Mittendorfer

Senior Associate Dean for Research; Professor, Medicine & Nutrition; NextGen Director of Clinical and Translational Sciences Unit

University of Missouri-Columbia

研究点 (1)

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