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Biol Trace Elem Res ; 155(1): 1-4, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23921483

ABSTRACT

Chromium is required for a normal insulin function, and low levels have been linked with insulin resistance. The aim of this study was to follow the effect of chromium supplementation on fasting plasma glucose (FPG), glycated haemoglobin (HbA1c) and serum lipids in patients with type 2 diabetes mellitus (DM2) on insulin therapy. Eleven randomly selected patients with DM2 on insulin therapy were supplemented with a daily dose of 100 µg chromium yeast for the first supplementation period of 2 weeks. In the second supplementation period, the chromium dose was doubled and continued for the next 6 weeks. The third phase was a 6-week washout period. After each period, the levels of FPG and HbA1c were compared with the corresponding values at the end of the previous period. Serum triglycerides, total HDL and LDL cholesterol values after supplementation were compared with the baseline values. FPG decreased significantly after the first period of chromium supplementation (p < 0.001), and a tendency to a further reduction was observed after the second supplementation period. Similarly, HbA1c decreased significantly in both periods (p < 0.02 and p < 0.002, respectively). Eight weeks after withdrawal of chromium supplementation, both FPG and HbA1c levels returned to their pre-intervention values. The serum lipid concentrations were not significantly influenced by chromium supplementation. Chromium supplementation could be beneficial in patients with DM2 treated with insulin, most likely due to lowered insulin resistance leading to improved glucose tolerance. This finding needs to be confirmed in a larger study.


Subject(s)
Blood Glucose/metabolism , Chromium/administration & dosage , Diabetes Mellitus, Type 2/drug therapy , Glycated Hemoglobin/metabolism , Insulin/therapeutic use , Lipids/blood , Yeast, Dried/administration & dosage , Adult , Aged , Aged, 80 and over , Diabetes Mellitus, Type 2/blood , Dietary Supplements , Drug Administration Schedule , Fasting/blood , Female , Humans , Hypoglycemic Agents/therapeutic use , Male , Middle Aged , Time Factors , Treatment Outcome
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