Journal of Advances in Medical and Biomedical Research

fa اثر درمان سه دارویی خوراکی در کنترل قند و لیپید بیماران مبتلا به دیابت تیپ 2 The Effects of Triple-Therapy in Metabolic Control of Patients Suffering from Type 2 Diabetic Mellitus (DM) Background and Objective: Although patients with uncontrolled type 2 Diabetes mellitus(DM) despite conventional treatment with oral hypoglycemic agents eventually require insulin to achieve glycemic control, most of them reject use of insulin. To evaluate the efficacy of adding acarbose to full doses of conventional oral hypoglycemic agents on the metabolic control of the patients this study was designed. Materials and Methods: In this uncontrolled follow-up study, 20 patients with type 2 DM and persistent poor glycemic control despite maximal doses of sulfonylurea and metformin were recruited to receive additional treatment with acarbose. Insulin therapy was rejected by all the patients and 12 weeks of dietary reinforcement and supervision for their diet and exercise programs failed to improve their glycemic control. An active treatment period with acarbose 100 mg thrice daily was fallowed by a 12-week of placebo. Efficacy was assessed by changes in HbA1c, fasting and 2-h postprandial plasma glucose and fasting plasma lipid levels. Results: Acarbose treatment was associated with significantly greater reductions in HbA1c (-1.3 +/- 0.2% vs. placebo 0.2 +/- 0.1%, P = 0.038), Fasting Plasma Glucose(FPG)(-25.3 +/-10 mg/dl vs. placebo 10 +/- 6mg/dl , p:0.019), 2-h postprandial glucose (-24 +/- 8 mg/dl vs. placebo   15+/- 7.5 mg/dl, P :0.001) and body mass index(BMI) (-0.5 +/- 0.32 kg/m² vs. placebo 0.42 +/- 0.29 kg/ m², P: 0.01). There were no significant changes in plasma lipids levels. Conclusion: In patients with type 2 DM inadequately controlled on conventional oral agents, acarbose resulted in beneficial effects on glycemic control and mean body weight. Additional use of acarbose can be considered as a useful alternative in such patients if they are reluctant to accept insulin therapy.Background and Objective: Although patients with uncontrolled type 2 Diabetes mellitus(DM) despite conventional treatment with oral hypoglycemic agents eventually require insulin to achieve glycemic control, most of them reject use of insulin. To evaluate the efficacy of adding acarbose to full doses of conventional oral hypoglycemic agents on the metabolic control of the patients this study was designed. Materials and Methods: In this uncontrolled follow-up study, 20 patients with type 2 DM and persistent poor glycemic control despite maximal doses of sulfonylurea and metformin were recruited to receive additional treatment with acarbose. Insulin therapy was rejected by all the patients and 12 weeks of dietary reinforcement and supervision for their diet and exercise programs failed to improve their glycemic control. An active treatment period with acarbose 100 mg thrice daily was fallowed by a 12-week of placebo. Efficacy was assessed by changes in HbA1c, fasting and 2-h postprandial plasma glucose and fasting plasma lipid levels. Results: Acarbose treatment was associated with significantly greater reductions in HbA1c (-1.3 +/- 0.2% vs. placebo 0.2 +/- 0.1%, P = 0.038), Fasting Plasma Glucose(FPG)(-25.3 +/-10 mg/dl vs. placebo 10 +/- 6mg/dl , p:0.019), 2-h postprandial glucose (-24 +/- 8 mg/dl vs. placebo   15+/- 7.5 mg/dl, P :0.001) and body mass index(BMI) (-0.5 +/- 0.32 kg/m² vs. placebo 0.42 +/- 0.29 kg/ m², P: 0.01). There were no significant changes in plasma lipids levels. Conclusion: In patients with type 2 DM inadequately controlled on conventional oral agents, acarbose resulted in beneficial effects on glycemic control and mean body weight. Additional use of acarbose can be considered as a useful alternative in such patients if they are reluctant to accept insulin therapy. Type 2 Diabetes mellitus, Acarbose, Blood Sugar, HbA1C, Lipid profile 17 26 http://journal.zums.ac.ir/browse.php?a_code=A-10-4-73&slc_lang=fa&sid=1 Vahdat Zanburi وحدت زنبوری 5200319475328460057915 5200319475328460057915 No Sardodin Kalantari صدرالدین کلانتری 5200319475328460057916 5200319475328460057916 No Faranak Sharifi فرانک شریفی faranaksharifi@hotmail.com 5200319475328460057917 5200319475328460057917 Yes Vali-e-Asr Hospital, Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran