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临床试验/NCT02420054
NCT02420054Unknown不适用

Effects of Short Term Intermittent Fasting on Insulin Resistance in Type 2 Diabetes

University of Copenhagen2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2015年4月最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
2
主要终点
Change of insulin secretion

研究概览

简要总结

The purpose of the study is to determine the effect of intermittent fasting on insulin secretion and insulin sensitivity in skeletal muscle and fat distribution.

详细描述

Approximately 250.000 patients are diagnosed with type 2 diabetes (T2DM) in Denmark, and world-wide close to 350 million people suffer from diabetes. T2DM develops in genetically susceptible individuals as a result of excess energy intake and insufficient amount of daily physical activity. The pathophysiology encompasses a mismatch between the insulin secretory capacity and insulin sensitivity, predominantly manifested in skeletal muscle as insulin resistance. T2DM is associated with increased morbidity and mortality.

The disease is triggered by the individual lifestyle, and thereby the potential for prevention and reversal of the disease in its early years after diagnosis is quite large.

One potential way to improve glucose homeostasis is by intermittent fasting, also known as alternate day fasting. Intermittent fasting means switching between eating and fasting, and it is a variation of calorie restriction. Intermittent fasting has been studied in animals. Together with calorie restriction, intermittent fasting is the most efficient way to expand lifespan of many animal species without genetically altering them. A wide range of age related changes are delayed including beneficial effects on hypertension, degenerative brain disease, immune responses, DNA repair capacity and glucose homeostasis. Fat redistribution with fat translocating from between the organs and the liver to the subcutis.

Little is known about intermittent fasting in humans. In 2005 the investigators experimentally tested this concept in young healthy males and found that 15 days of alternating days with fast and food intake increased insulin sensitivity by 16% without any changes in body weight.

The explanation could be oscillations in cellular energy stores. Skeletal muscle contains approximately 80% of the stored glycogen alone by virtue of the muscle mass. The liver has a higher glycogen concentration, but it is much smaller. A single prolonged (>24 hrs) day of fasting may not decrease muscle glycogen, while the decrease in the liver is very fast. A muscle glycogen lowering effect of continued intermittent fasting would be expected, and experimentally indicated.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • BMI 28-35
  • Type 2 diabetes or metabolically healthy
  • Diet or orally administered treatment for type 2 diabetes

排除标准

  • Regular physical activity
  • Other diseases than type 2 diabetes
  • insulin treatment
  • alcohol abuse

结局指标

主要结局

Change of insulin secretion

时间窗: 46 days

IVGTT performed at baseline, after intermittent fasting without weight loss and again after intermittent fasting with weight loss

Change from Baseline in Insulin Sensitivity after 20 days of intermittent fasting.

时间窗: 46 days

An euglycemic hyperinsulinemic clamp is performed at day 1 and repeated at day 23 after a control period with no change in the diet. Baseline insulin sensitivity is determined based on these two measurements. The euglycemic hyperinsulinemic clamp is repeated at day 46 after the intermittent fasting period (day 25-44) and two days (day 24 and 45) with a normal diet.

次要结局

  • Glycogen Content in Skeletal Muscle after a Day of Eating and after a Day of Fasting(46 days)
  • Change from Baseline in Fat Content in the Liver and Visceral Fat after 20 Days of Intermittent Fasting(23 days)
  • Insulin signalling cascade proteins(46 days)

研究者

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

Flemming Dela

Professor

University of Copenhagen

研究点 (2)

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