The Effects of Metformin Monotherapy and Combination of Metformin and Glibenclamide Therapy on the Expression of , , and Genes in Peripheral Blood Mononuclear Cells of Type 2 Diabetic Patients
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Purpose: Although metformin is the first-line treatment of type 2 diabetes mellitus (T2DM), a few studies have evaluated the benefits of monotherapies (metformin) versus combination therapy (metformin and glibenclamide) for treatment of T2DM patients. The present study aimed to evaluate the effect of monotherapy with metformin compared to combination therapy with metformin and glibenclamide on the expression of , , and genes.
Methods: EightyT2DM patients and 40 healthy individuals participated in this case-control study. The patients in the treatment group were divided into two groups who received either metformin alone (n = 40) or metformin in combination with glibenclamide (n = 40). FBS, HbA1c, and fructosamine were measured. The expression of , , and genes in PBMC of all subjects were assessed using real-time PCR.
Results: gene expression in both treatment groups was significantly lower than the control (P < 0.05). gene expression was significantly reduced in the combination of metformin and glibenclamide treated group compared to metformin group (P < 0.05). Additionally, the expression of and genes in both treatment groups was higher than that of the control group (P < 0.05). The expression of and genes in metformin and glibenclamide treated group were higher than the metformin group (P < 0.05).
Conclusion: Combination therapy (metformin and glibenclamide) showed stronger effect on repression of the gene and activation of and genes compared to monotherapy (metformin); therefore, it can be concluded that combination therapy may have more protective effects on the T2DM patients. No significant correlation was observed between HbA1c and , , and genes expression.
Sirtuins and Their Implications in the Physiopathology of Gestational Diabetes Mellitus.
Zgutka K, Tkacz M, Grabowska M, Mikolajek-Bedner W, Tarnowski M Pharmaceuticals (Basel). 2025; 18(1).
PMID: 39861104 PMC: 11768332. DOI: 10.3390/ph18010041.