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临床试验/NCT02673515
NCT02673515已完成不适用

The Impact of Intermittent Fasting on Human Metabolism and Cell Autophagy

Medical University of Graz2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2015年4月1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
入组人数
60
试验地点
2
主要终点
Insulin Sensitivity (ISI-Index)

研究概览

简要总结

InterFast is a Cohort study with an embedded randomized controlled pilot trial. Study participants will be healthy subjects and subjects who already practice Alternate Day Fasting. The trial will include 100 participants (50 Participants in Alternate Day Fasting group and 50 participants in the control group). Those participants in the control group will be asked to participate in a short randomized controlled trial, where they will be either allocated to an Alternative Day Fasting group or another control visit.

详细描述

Intermittent fasting is a dietary regimen defined by alternating fasting and "feeding" cycles. In addition to caloric restriction (a dietary regimen limited to a daily food intake lower than one's daily caloric needs) only, intermittent fasting seems to activate cell autophagy (cellular "recycling" program) which potentially increases cellular stress resistance and removes accumulated molecules that are potentially toxic. In fact, mice maintained on intermittent fasting without decreased overall food intake show effects on body weight reduction that equal and in some cases even exceed those of calorie restriction. However, additionally, intermittent fasting combined with even a high-fat diet in the feeding periods protects mice from obesity, hyperinsulinemia, hepatic steatosis, and inflammation compared to controls that are fed an ad libitum high-fat diet despite the same calorie intake, making this intermittent fasting regimen a promising approach to reduce morbidity and mortality in various species.

The best described and most widely practiced version of intermittent fasting is the "alternate day diet" or "alternate day fasting" (ADF). In animal models, ADF consists of an ad libitum "feed day" alternated with a 100% restriction "fast day". However in humans, this is often modified to allow a small amount of food consumption on the "fast day" (e.g. 25% of the individual´s energy needs). Findings from recent modified ADF studies showed significant reductions in body weight.

However, knowledge about the molecular effects of the alternate day diet on human metabolism or autophagy is still scarce since detailed analyses of molecular and metabolic parameters remain unexplored, especially in healthy individuals. The overarching aim of this research project is to elucidate in which extent alternate day fasting (and thereby intermittent fasting) influences human physiology in healthy individuals in both short and long term. The secondary objective of this study is to define novel molecular markers of aging and age-related diseases.

研究设计

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

入排标准

年龄范围
35 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Body mass index in the range of 22.0 - 27.0 kg/m2,
  • Fasting blood glucose <110mg/dL (without medication)
  • LDL-cholesterol <180 mg/dL (without medication)
  • Blood pressure <140/90 mmHg (without medication)
  • Stable weight (change <± 10%) for 3 months immediately prior to the study,
  • No history of metabolic disorders or cardiovascular disease
  • No acute or chronic inflammatory disorder
  • No current medications to regulate blood sugar, blood pressure or lipids or hormones
  • No heavy drinking (more than 15 drinks/week)
  • No use of tobacco or recreational drugs within past 5 years
  • No dietary restrictions (e.g. vegetarianism and vegan)

排除标准

  • Known Malignancy
  • Women who are pregnant, breast-feeding or trying to become pregnant
  • History of any chronic disease process that could interfere with interpretation of study results
  • Women or men on hormonal supplementation or anti-conceptive hormonal medication for at least 2 months
  • Therapy with antidepressants within past 6 months
  • Regular therapy with acetylsalicylic acid

结局指标

主要结局

Insulin Sensitivity (ISI-Index)

时间窗: 4 weeks (from Baseline to 4 weeks)

ISI was calculated by using the following formula: ISI=0,222-0,00333 x BMI-0,0000779 x Ins120-0,000422 x age FSI=fasting serum insulin FPG=fasting plasma glucose

Insulin Sensitivity (Matsuda-Index)

时间窗: 4 weeks (from Baseline to 4 weeks)

Matsuda index was calculated by using the following formula: Matsuda-Index = 10000√(FPG∗FSI)∗(mean glucose\*mean insulin) FSI=fasting serum insulin FPG=fasting plasma glucose

Insulin Sensitivity (HOMA-IR)

时间窗: 4 weeks (from Baseline to 4 weeks)

HOMA-Index was calculated by using the following formula: HOMA-IR= FPG(mmol/l)\*FSI (U/l)/22.5 FSI=fasting serum insulin FPG=fasting plasma glucose

Insulin Sensitivity (QUICKI)

时间窗: 4 weeks (from Baseline to 4 weeks)

QUICKI was calculated by using the following formula: QUICKI= log(FSI)+log (FPG) FSI=fasting serum insulin FPG=fasting plasma glucose

次要结局

  • Blood Pressure (Systolic and Diastolic)(4 weeks)

研究者

发起方
Medical University of Graz
申办方类型
Other
责任方
Sponsor

研究点 (2)

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