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临床试验/NCT00968747
NCT00968747已完成不适用

The Effect of Acute Nutritional Challenges on FGF21 Levels in Humans

Beth Israel Deaconess Medical Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2009年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Fibroblast Growth Factor 21 levels in serum and fat

研究概览

简要总结

The purpose of this study is to examine how acute nutritional challenges affect levels of several proteins involved in metabolism. These proteins will be measured in blood and fat tissue.

This study will have several aims.

One aim is to examine the effect of 72 hours of fasting on fibroblast growth factor-21 (FGF-21) levels. Participants will spend 3 days and nights in the Clinical Research Center at the Beth Israel Deaconess Medical Center in Boston, MA. Daily blood samples will be taken. Two fat samples will be taken prior to and at the end of the fast. A subset of participants will also have two MRIs, one prior to and one at the end of the fast. We will study healthy adults and obese adults with liver-biopsy-diagnosed non-alcoholic fatty liver disease (NAFLD). THIS STUDY ARM IS CURRENTLY NOT RECRUITING

Another aim is to examine the effect of low-calorie diet on FGF-21 levels. Subjects will follow a hypocaloric diet that will be designed to achieve 3-5% weight loss. We will enroll participants with liver-biopsy-diagnosed non-alcoholic fatty liver disease. Participants will report weekly to the Clinical Research Center at Beth Israel Deaconess Medical Center for weight measurements. Blood will be drawn before and after the weight loss. Participants will also have an MRI before and after the weight loss.

THIS ARM IS CURRENTLY NOT RECRUITING

Another aim of the study is to examine the effect of acute ingestion of glucose, fructose, and other sugars on serum FGF21 levels. Subjects in this study will be lean volunteers and individuals with metabolic syndrome.

THIS ARM IS CURRENTLY RECRUITING

详细描述

Participation in this study involves fasting overnight, drinking a sweet beverage, and several blood draws through an IV line. Each subject may drink up to 5 different sweet beverages, separated by 2 weeks.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-50 years
  • Body Mass Index 21-26 kg/m^2
  • Ability to give informed consent
  • Ability to follow verbal and written instructions in English

排除标准

  • Type 1 or Type 2 diabetes mellitus diagnosed according to the American Diabetes Association criteria
  • Coronary heart disease (history of myocardial infarction, unstable angina pectoris, or congestive heart failure)
  • Tobacco, marijuana, or intravenous drug use within 1 year of screening visit
  • Recent weight change (>3 kg within 6 months of screening visit)
  • Malignancy treated with chemotherapy within past 3 years
  • History of depression, psychosis, or other psychiatric illness requiring hospitalization
  • History of hyperthyroidism
  • Renal insufficiency (creatinine clearance < 50 ml/min)
  • Transaminases > 2X above the normal range
  • Known liver disease
  • Pregnancy within 12 months of screening visit
  • Lactation within 12 months of screening visit
  • Failure to use medically approved contraceptive methods (oral contraceptive, 2 barrier methods, surgical sterilization)
  • History of an eating disorder (anorexia, bulimia, or laxative abuse)
  • History of surgery for the treatment of obesity (gastric banding, gastric bypass, gastric stapling)
  • New diagnosis of hypothyroidism within 1 year of screening visit or change in dose of thyroid hormone within 3 months of screening visit
  • History of alcohol abuse within the past 3 years
  • History of keloid formation
  • History of allergy to lidocaine or marcaine
  • Use of plavix, coumadin, or heparin
  • 72-hour fast or hypocaloric diet in subjects with non-alcoholic fatty liver disease (NAFLD) (Study Arms B & C):
  • Inclusion Criteria:
  • Age 18-60
  • BMI 25-45 kg/m^2
  • Known nonalcoholic fatty liver disease based on liver biopsy
  • Ability to give informed consent
  • Ability to follow verbal and written instructions in English
  • Exclusion Criteria:
  • Type I diabetes mellitus diagnosed according to the American Diabetes Association criteria or Type II diabetes mellitus with A1c > 7.5% or taking metformin or thiazolidinediones
  • Coronary Heart Disease (history of myocardial infarction, unstable angina pectoris, or congestive heart failure)
  • Uncontrolled hypertension (BP > 150/90 mmHg on or off antihypertensive medication)
  • Tobacco, marijuana, or intravenous drug use within 1 year of screening visit
  • Recent weight change (> 3 kg within 6 months of screening visit)
  • Malignancy treated with chemotherapy within the past 3 years
  • History of depression, psychosis, or other psychiatric illness requiring hospitalization
  • History of hypo or hyperthyroidism
  • Renal insufficiency (creatinine clearance < 50 ml/min)
  • Pregnancy within 12 months of screening visit
  • Lactation within 12 months of screening visit
  • Failure to use medically approved contraceptive methods (oral contraceptive, 2 barrier methods, surgical sterilization)
  • History of an eating disorder (anorexia, bulimia, or laxative abuse)
  • History of surgery for the treatment of obesity (gastric banding, gastric bypass, gastric stapling)
  • New diagnosis of hypo or hyperthyroidism within 1 year of screening visit or change in dose of thyroid hormone within 3 months of screening visit
  • History of alcohol abuse within the past 3 years
  • Cardiac pacemaker or aneurysm clips
  • Metal implants in the body (pins, plates, shrapnel, intact bullets, IUD)
  • Claustrophobia

结局指标

主要结局

Fibroblast Growth Factor 21 levels in serum and fat

时间窗: before and after dietary intervention

Change in FGF21 levels following nutritional intervention.

次要结局

  • Hepatic fat content(Before and after the 72-hour fast or hypocaloric diet in participants with NAFLD)
  • Urine and serum ketosis(Daily during the 72-hour fast for healthy participants and participants with NAFLD)
  • change in serum triglyceride levels(following fructose and glucose ingestion)
  • Polymerase 1 and Transcript Release Factor levels in fat(Prior to fasting and at the end of the 72-hour fast in healthy participants and participants with NAFLD)
  • change in glucose and insulin levels(following fructose and glucose ingestion)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jody Dushay

MD

Beth Israel Deaconess Medical Center

研究点 (2)

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