The Glucose-Lowering Effect of Foxtail Millet in Subjects with Impaired Glucose Tolerance: A Self-Controlled Clinical Trial

Nutrients. 2018 Oct 15;10(10):1509. doi: 10.3390/nu10101509.

Abstract

Foxtail millet has relatively low starch digestibility and moderate glycemic index compared to other grains. Since there are still no clinical researches regarding its long-term effect on blood glucose, this self-controlled study was conducted to investigate the glucose-lowering effect of foxtail millet in free-living subjects with impaired glucose tolerance (IGT). Fifty g/day of foxtail millet was provided to enrolled subjects throughout 12 weeks and the related clinical parameters were investigated at week 0, 6 and 12, respectively. After 12 weeks of foxtail millet intervention, the mean fasting blood glucose of the subjects decreased from 5.7 ± 0.9 mmol/L to 5.3 ± 0.7 mmol/L (p < 0.001) and the mean 2 h-glucose decreased from 10.2 ± 2.6 mmol/L to 9.4 ± 2.3 mmol/L (p = 0.003). The intake of foxtail millet caused a significant increase of serum leptin (p = 0.012), decrease of insulin resistance (p = 0.007), and marginal reduction of inflammation. Furthermore, a sex-dependent difference in glucose-lowering effect of foxtail millet was observed in this study. Foxtail millet could improve the glycemic control in free-living subjects with IGT, suggesting that increasing the consumption of foxtail millet might be beneficial to individuals suffering from type 2 diabetes mellitus.

Keywords: blood glucose; dietary intervention; impaired glucose tolerance; whole foxtail millet.

Publication types

  • Controlled Clinical Trial

MeSH terms

  • Biomarkers / blood
  • Blood Glucose / metabolism*
  • Bread*
  • China
  • Cooking
  • Female
  • Glucose Intolerance / blood
  • Glucose Intolerance / diagnosis
  • Glucose Intolerance / diet therapy*
  • Humans
  • Inflammation Mediators / blood
  • Insulin / blood
  • Insulin Resistance
  • Leptin / blood
  • Male
  • Middle Aged
  • Nutritive Value
  • Recommended Dietary Allowances
  • Setaria Plant*
  • Time Factors
  • Treatment Outcome

Substances

  • Biomarkers
  • Blood Glucose
  • Inflammation Mediators
  • Insulin
  • Leptin