Failure of beta-cell function for compensate variation in insulin sensitivity in hypomagnesemic subjects

Magnes Res. 2009 Sep;22(3):151-6.

Abstract

To evaluate if decreased insulin sensitivity is appropriately compensated by beta-cell function in subjects with hypomagnesemia, 165 individuals, 20 to 65 years of age, were randomly enrolled in a cross-sectional study. Subjects were allocated into groups with and without hypomagnesemia, matched by age, gender, waist circumference, and body mass index. Pregnancy, smoking, alcohol consumption, high blood pressure, type 2 diabetes, chronic diarrhea, renal disease, malignancy, and heavy physical activity were exclusion criteria. Hypomagnesemia was defined by a serum magnesium concentration of < 1.8 mg/dL. As a surrogate of the hyperbolic model of beta-cell function, the relation between Belfiore's index {2/[1 + (Fasting insulin pmol/L x Fasting glucose mmol/L)]} and the HOMA-beta index {20 X Fasting insulin microU/mL /(Fasting glucose mmol/L - 3.5)} was used. The mean Area Under Curve (AUC) was calculated for each group. Although the Belfiore index was significantly lower (0.041 +/- 0.021 and 0.053 +/- 0.030, p = 0.005) and fasting plasma glucose higher (113.6 +/- 23.0 and 106.8 +/- 18.4 mg/dL, p = 0.04) in the subjects with hypomagnesemia, the HOMA-beta index (82.5 +/- 48.5 and 91.2 +/- 79.9, p = 0.32) and insulin levels (8.6 +/- 5.4 and 9.6 +/- 4.8 mciroU/mL, p = 0.17) were similar between the groups studied. The AUC which evaluates the adaptation of beta-cell function to variation in insulin sensitivity was significantly higher in the normo-magnesemic than the hypomagnesemic group (proportion 1:2.5). Results of this study show that the decrease in insulin sensitivity is not appropriately compensated by beta-cell function in individuals with hypomagnesemia; our finding suggests that hypomagnesemia could be linked to inadequate beta-cell compensation.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Female
  • Humans
  • Insulin Resistance*
  • Insulin-Secreting Cells / pathology*
  • Magnesium Deficiency*
  • Male
  • Middle Aged
  • Young Adult