Effects of enteral carbohydrates on de novo lipogenesis in critically ill patients

Am J Clin Nutr. 2000 Oct;72(4):940-5. doi: 10.1093/ajcn/72.4.940.

Abstract

Background: Conversion of glucose into lipid (de novo lipogenesis; DNL) is a possible fate of carbohydrate administered during nutritional support. It cannot be detected by conventional methods such as indirect calorimetry if it does not exceed lipid oxidation.

Objective: The objective was to evaluate the effects of carbohydrate administered as part of continuous enteral nutrition in critically ill patients.

Design: This was a prospective, open study including 25 patients nonconsecutively admitted to a medicosurgical intensive care unit. Glucose metabolism and hepatic DNL were measured in the fasting state or after 3 d of continuous isoenergetic enteral feeding providing 28%, 53%, or 75% carbohydrate.

Results: DNL increased with increasing carbohydrate intake (f1.gif" BORDER="0"> +/- SEM: 7.5 +/- 1.2% with 28% carbohydrate, 9.2 +/- 1.5% with 53% carbohydrate, and 19.4 +/- 3.8% with 75% carbohydrate) and was nearly zero in a group of patients who had fasted for an average of 28 h (1.0 +/- 0.2%). In multiple regression analysis, DNL was correlated with carbohydrate intake, but not with body weight or plasma insulin concentrations. Endogenous glucose production, assessed with a dual-isotope technique, was not significantly different between the 3 groups of patients (13.7-15.3 micromol * kg(-1) * min(-1)), indicating impaired suppression by carbohydrate feeding. Gluconeogenesis was measured with [(13)C]bicarbonate, and increased as the carbohydrate intake increased (from 2.1 +/- 0.5 micromol * kg(-1) * min(-1) with 28% carbohydrate intake to 3.7 +/- 0.3 micromol * kg(-1) * min(-1) with 75% carbohydrate intake, P: < 0. 05).

Conclusion: Carbohydrate feeding fails to suppress endogenous glucose production and gluconeogenesis, but stimulates DNL in critically ill patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Blood Glucose / analysis
  • Calorimetry, Indirect
  • Carbohydrate Metabolism*
  • Carbohydrates / administration & dosage
  • Chromatography, High Pressure Liquid
  • Critical Care / methods
  • Enteral Nutrition / methods*
  • Fatty Acids / blood
  • Female
  • Gas Chromatography-Mass Spectrometry
  • Glucagon / blood
  • Gluconeogenesis
  • Glucose / biosynthesis
  • Glucose / metabolism
  • Humans
  • Hydrocortisone / blood
  • Insulin / analysis
  • Kinetics
  • Lipids / biosynthesis*
  • Liver / metabolism
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Prospective Studies
  • Radioimmunoassay
  • Random Allocation
  • Regression Analysis
  • Triglycerides / blood

Substances

  • Blood Glucose
  • Carbohydrates
  • Fatty Acids
  • Insulin
  • Lipids
  • Triglycerides
  • Glucagon
  • Glucose
  • Hydrocortisone