4.7 Article

Glycemic Control and Metabolic Adaptation in Response to High-Fat versus High-Carbohydrate Diets-Data from a Randomized Cross-Over Study in Healthy Subjects

期刊

NUTRIENTS
卷 13, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/nu13103322

关键词

glucose; insulin; metabolism; glucagon-like peptide-1; high-fat; high-carbohydrate; diet

资金

  1. western region of Sweden [ALFGBG-721551]
  2. Gothenburg Medical Association and the Erik

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In this study, healthy normal-weight volunteers showed similar postprandial glycemic and insulin responses to high-fat and high-carbohydrate diets. However, the high-fat diet exhibited a metabolomic pattern suggesting a potential shift towards insulin resistance in the long term.
Granular study of metabolic responses to alterations in the ratio of dietary macro-nutrients can enhance our understanding of how dietary modifications influence patients with impaired glycemic control. In order to study the effect of diets enriched in fat or carbohydrates, fifteen healthy, normal-weight volunteers received, in a cross-over design, and in a randomized unblinded order, two weeks of an iso-caloric high-fat diet (HFD: 60E% from fat) and a high-carbohydrate diet (HCD: 60E% from carbohydrates). A mixed meal test (MMT) was performed at the end of each dietary period to examine glucose clearance kinetics and insulin and incretin hormone levels, as well as plasma metabolomic profiles. The MMT induced almost identical glycemia and insulinemia following the HFD or HCD. GLP-1 levels were higher after the HFD vs. HCD, whereas GIP did not differ. The HFD, compared to the HCD, increased the levels of several metabolomic markers of risk for the development of insulin resistance, e.g., branched-chain amino acid (valine and leucine), creatine and alpha-hydroxybutyric acid levels. In normal-weight, healthy volunteers, two weeks of the HFD vs. HCD showed similar profiles of meal-induced glycemia and insulinemia. Despite this, the HFD showed a metabolomic pattern implying a risk for a metabolic shift towards impaired insulin sensitivity in the long run.

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