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临床试验/NCT03341052
NCT03341052已完成不适用

Characterization of Bile Acid Pathway in Obesity

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2017年11月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
16
试验地点
2
主要终点
Change in 48h-fecal Bile Acid Excretion (μmol/L) Between Baseline and High Fat Diet

研究概览

简要总结

It is unknown whether the bile acid pathway is altered in obesity. This study is designed to compare obesity and health to determine if the bile acid pathway differs depending on health state.

详细描述

This is a single center study involving diet intervention, including healthy obese and healthy normal weight participants. Participants will maintain their normal diet for 1 week, eat a high fat and high calorie diet for 1 week, return to their normal diet for 1 week, and eat a low fat and low calorie diet for 1 week, to study the effect of diet on the bile acid pathway in normal weight and obesity. During their first normal diet week, the high calorie week, and the low calorie week, blood samples will be collected at defined times to measure cholesterol, glycemia, Fibroblast Growth Factor 19 (FGF-19), Bile Acid (BA), C4, and incretins (GLP-1 (glucagon-like peptide-1), peptide tyrosine tyrosine (PYY 3-36)) fasting levels and responses to the meal. Stool samples will be collected for 48 hour BA excretion.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Women of childbearing potential will have negative pregnancy tests within 48 hours of enrollment
  • BMI: 18.5-25 kg/m2
  • Obese Inclusion Criteria:
  • Women of childbearing potential will have negative pregnancy tests within 48 hours of enrollment
  • BMI: ≥ 30 kg/m2
  • Exclusion Criteria for both Normal Weight and Obese Participants:
  • History of abdominal surgery including cholecystectomy and other than appendectomy, Caesarian section or tubal ligation.
  • Positive history of chronic gastrointestinal diseases, or systemic disease that could affect gastrointestinal motility, or use of medications that may alter gastrointestinal motility, appetite or absorption, e.g., orlistat, phentermine.
  • Significant untreated psychiatric dysfunction based upon screening with the Hospital Anxiety and Depression Inventory (HAD), a self-administered alcoholism screening test (AUDIT-C) and the Questionnaire on Eating and Weight Patterns (binge eating disorders and bulimia). If such a dysfunction is identified by a HAD score >11 or difficulties with substance or eating disorders, the participant will be excluded and given a referral letter to his/her primary care doctor for further appraisal and follow-up. The AUDIT-C is a 3-item alcohol screening questionnaire that reliably identifies participants who are hazardous alcohol drinkers or have active alcohol use disorders. In men, a score of 4 or more is above the recommended limits will be reviewed by study personnel. In women, a score of 3 or more is above the recommended limits will be reviewed by study personnel. However when the points are above recommended limits, the provider will review the patient's alcohol intake over the past few months to confirm accuracy and determine study eligibility..
  • Intake of medication, whether prescribed or over the counter (except multivitamins), within 7 days of the study. Exceptions are birth control pill, estrogen replacement therapy, and thyroxin replacement therapy.

排除标准

  • 未提供

结局指标

主要结局

Change in 48h-fecal Bile Acid Excretion (μmol/L) Between Baseline and High Fat Diet

时间窗: Baseline to approximately day 7 of week 2

Change in 48h-fecal bile acid excretion (μmol/L) between baseline and high fat diet

Change in 48h-fecal Bile Acid Excretion (μmol/L) Between Baseline and Low Fat Diet

时间窗: Baseline to approximately day 7 of week 4

Change in 48h-fecal bile acid excretion (μmol/L) between baseline and low fat diet

次要结局

未报告次要终点

研究者

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

Andres J. Acosta, M.D., Ph.D.

Principal Investigator

Mayo Clinic

研究点 (2)

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