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临床试验/NCT01064778
NCT01064778已完成不适用

The Effects of Dietary Glycemic Index on Brain Function

Beth Israel Deaconess Medical Center6 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2010年2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
12
试验地点
6
主要终点
Blood Flow in Brain Areas of Intake Control.

研究概览

简要总结

The investigators propose examine the effects of the dietary factor glycemic index (GI) on brain areas that control food intake and hunger. This knowledge could help design dietary approaches that decrease hunger, and thus promote new weight loss strategies.

详细描述

Most individuals have great difficulty following reduced calorie diets because they experience increased hunger. This process is regulated by specific brain areas. Though many psychological and environmental factors are involved, physiological effects of diet may have a significant impact. The postprandial rise in blood glucose, quantified by the glycemic index (GI), is of particular interest. High GI meals elicit hormonal events that limit availability of metabolic fuels, causing hunger and overeating, especially in people with high insulin secretion.

Our aim is to examine how postprandial changes after high versus low GI meals affect hunger and brain function in areas of intake control. Specifically, we speculate that obese individuals will demonstrate functional changes in brain areas of intake control and increased hunger after a high versus low GI meal.

We will recruit obese, young adults and quantify their insulin secretion during a 2-hour oral glucose tolerance test. A brief practice MRI session will serve to familiarize the subjects with the scanning process. During the two test sessions, standardized test meals with high versus low GI will be given in a randomized, blinded cross-over design. Serial blood levels of hormones, metabolic fuels, and metabolites will be correlated with perceived hunger, and a perfusion MRI scan will be performed to assess brain activation during the late postprandial phase, at the nadir of blood sugar and insulin levels (4 hours postprandial).

This work will inform an integrated physiological model relating peripheral postprandial changes to brain function and hunger. In addition, findings may provide evidence of a novel diet-phenotype, in which baseline clinical characteristics can be used to predict which weight loss diet will work best for a specific individual. Metabolite profiling might shed light on the mechanisms linking diet composition to brain function, and provide feasible clinical markers of the identified phenotype to facilitate translation into practice.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Blood Flow in Brain Areas of Intake Control.

时间窗: 4 hours postprandial

次要结局

  • Blood Glucagon Level(Every 30 minutes for 5 hours.)
  • Blood Growth Hormone Level(Every 30 minutes for 5 hours.)
  • Subjective Hunger Rating(Every 30 minutes for 5 hours.)
  • Blood Glucose Level(Every 30 minutes for 5 hours.)
  • Blood Insulin Level(Every 30 minutes for 5 hours)
  • Blood Epinephrine Level(Every 30 minutes for 5 hours.)
  • Blood Fatty Acids Level(Every 30 minutes for 5 hours.)

研究者

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

David Alsop

Director of MRI Research

Beth Israel Deaconess Medical Center

研究点 (6)

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