Abstract | OBJECTIVE:
Type 2 diabetes mellitus is characterized by insulin resistance and defects in insulin secretion from pancreatic beta-cells, which have been studied by using euglycemic/hyperinsulinemic clamps. However, it is difficult to study insulin resistance and beta-cell failure by these techniques in humans. Therefore, the aim of this study was to evaluate the effect of three different antidiabetic therapeutic regimens on insulin resistance and beta-cell activity by using a mathematical model, Homeostasis Model Assessment for insulin resistance (HOMA(IR)) and beta-cell function (HOMA(beta-cell)). RESEARCH DESIGN AND METHODS: Seventy type 2 diabetic patients were randomly assigned to one of three therapeutic regimens: (A) metformin + American Diabetic Association (ADA)-recommended diet + physical activity; (B) metformin + low-dose glimepiride + ADA diet + physical activity; or (C) ADA diet + physical activity (no drugs). Blood samples were obtained before and after the treatment to determine serum levels of fasting and post-prandial blood glucose, fasting insulin, and glycosylated hemoglobin (HbA1c), and HOMA(IR) and HOMA(beta-cell) were calculated. RESULTS: Fasting and post-prandial levels of glucose, HbA1c, and fasting insulin and calculated HOMA(IR) and HOMA(beta-cell) values before treatment were significantly higher than the respective values after treatment for all groups of patients (P < 0.01). Significant differences were also found when comparing the treatment-induced reduction in fasting blood glucose (51.8%; P < 0.01), post-prandial blood glucose (55.0%; P < 0.05), and HOMA(IR) (65.3%; P < 0.01) in patients of Group B with that in patients receiving other therapeutic options (Groups A and C). CONCLUSIONS:
Metformin plus low-dose glimepiride (plus ADA diet and physical activity) is a more effective treatment for type 2 diabetes than either metformin plus ADA diet and physical activity or ADA diet and physical activity alone. Determination of HOMA(IR) and HOMA(beta-cell) values is an inexpensive, reliable, less invasive, and less labor-intensive method than other tests to estimate insulin resistance and beta-cell function in patients with type 2 diabetes mellitus.
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Authors | Valmore J Bermúdez-Pirela, Clímaco Cano, Mayerlim T Medina, Aida Souki, Miguel A Lemus, Elliuz M Leal, Hamid A Seyfi, Raquel Cano, Ana Ciscek, Fernando Bermúdez-Arias, Freddy Contreras, Zafar H Israili, Rafael Hernández-Hernández, Manuel Valasco |
Journal | American journal of therapeutics
(Am J Ther)
2007 Mar-Apr
Vol. 14
Issue 2
Pg. 194-202
ISSN: 1075-2765 [Print] United States |
PMID | 17414590
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- Blood Glucose
- Glycated Hemoglobin A
- Hypoglycemic Agents
- Insulin
- Sulfonylurea Compounds
- glimepiride
- Metformin
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Topics |
- Blood Glucose
(analysis)
- Diabetes Mellitus, Type 2
(complications, drug therapy, therapy)
- Diet
- Drug Therapy, Combination
- Female
- Glycated Hemoglobin
(analysis)
- Humans
- Hyperinsulinism
(complications)
- Hypoglycemic Agents
(administration & dosage, therapeutic use)
- Insulin
(metabolism)
- Insulin Resistance
- Insulin-Secreting Cells
(drug effects)
- Male
- Metformin
(administration & dosage, therapeutic use)
- Middle Aged
- Models, Biological
- Motor Activity
- Sulfonylurea Compounds
(administration & dosage, therapeutic use)
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