HYPOMAGNESEMIA IN TYPE-II DIABETES - EFFECT OF A 3-MONTH REPLACEMENT THERAPY

OBJECTIVE- To investigate the effects of long-term high-dose oral magn esium (Mg) therapy (30 mmol/day) in patients with type II diabetes. Lo w plasma magnesium levels have been reported in type II diabetes and a re associated with insulin resistance and diabetic late complications. RESEARCH DESIGN AND METHODS- Forty patients with type II diabetes and hypomagnesemia were observed in a randomized double-blind placebo-con trolled trial for 3 months (body mass index: 28 +/- 4 kg/m(2); HbA(1c) : 7.4 +/- 0.8%). Plasma and urine magnesium and metabolic control para meters were determined, and side effects were considered, especially w ith regard to patients' compliance. RESULTS- A significant increase in plasma magnesium levels was observed after 3 months of treatment (Mg: 0.73 +/- 0.8 vs. 0.81 +/- 0.1 mmol/l), reaching magnesium levels of t he control group (0.88 +/- 0.8 mmol/l; NS); metabolic control, however , was not altered (HbA(1c): 7.2 +/- 0.7 vs. 7.4 +/- 0.9%). Six months after the end of the trial, plasma magnesium declined to pretreatment levels (Mg: 0.73 +/- 0.07 mmol/l). The prevalence of side effects was high at the beginning and was reduced significantly during treatment. CONCLUSIONS- We conclude that oral magnesium replacement therapy corre cts hypomagnesemia after a minimum treatment period of 3 months. These observations might be important for the prevention of diabetic late c omplications.