Lack of detectable deleterious effects on metabolic control of daily fructose ingestion for 2 mo in NIDDM patients

Diabetes Care. 1988 Jul-Aug;11(7):546-50. doi: 10.2337/diacare.11.7.546.

Abstract

The effects of a daily intake of 30 g fructose on blood glucose regulation, erythrocyte insulin receptors, and lipid metabolism have been studied in type II (non-insulin-dependent) diabetic subjects. Eight well-controlled patients received, in a randomly assigned crossover design over two 2-mo study periods, 30 g of fructose in exchange for an isocaloric amount of starch. Fructose could be taken at any time during the day as part of the 1400-1600 kcal allowed diet (50% carbohydrate, 30% fat, 20% protein). No significant difference was observed concerning body weight, HbA1c, fasting plasma glucose, fasting plasma insulin, uric acid, total cholesterol, high-density lipoprotein cholesterol, and triglycerides, nor was there any change in insulin binding to erythrocytes between the fructose and the control starch period. However, the mean plasma triglyceride levels after the fructose period, although still in the normal range, were significantly higher than baseline values (P less than .05). We conclude that moderate amounts of fructose incorporated into the diet of well-controlled type II diabetic subjects have no significant deleterious effect on glycemic control, insulin receptors of erythrocytes, or lipid metabolism.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose / metabolism*
  • Cholesterol / blood
  • Cholesterol, HDL / blood
  • Diabetes Mellitus, Type 2 / blood*
  • Dietary Carbohydrates*
  • Erythrocytes / metabolism
  • Fructose*
  • Glycated Hemoglobin / analysis
  • Humans
  • Receptor, Insulin / analysis
  • Triglycerides / blood
  • Uric Acid / blood

Substances

  • Blood Glucose
  • Cholesterol, HDL
  • Dietary Carbohydrates
  • Glycated Hemoglobin A
  • Triglycerides
  • Uric Acid
  • Fructose
  • Cholesterol
  • Receptor, Insulin