首页> 外文期刊>Journal of Diabetology: Official Journal of Diabetes in Asia Study Group >Comparison of efficacy of add-on therapy of teneligliptin versus pioglitazone among type 2 diabetes mellitus patients ineptly controlled on dual therapy of metformin plus sulfonylurea
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Comparison of efficacy of add-on therapy of teneligliptin versus pioglitazone among type 2 diabetes mellitus patients ineptly controlled on dual therapy of metformin plus sulfonylurea

机译:替格列汀和吡格列酮联合治疗在二甲双胍联合磺脲类药物联合治疗无效的2型糖尿病患者中的疗效比较

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Aim: The main aim of the study is to compare the efficacy of add-on therapy of teneligliptin (20 once daily) versus pioglitazone (15 mg once daily) among type 2 diabetes mellitus (T2DM) patients inadequately controlled on dual therapy of metformin (MF) plus sulfonylurea (SU). Materials and Methods: It is a prospective, observational, comparative study conducted in patients from the outpatient department of Sri Bhadrakali Hospital located at Warangal, Telangana state, India. The efficacy of pioglitazone and teneligliptin was assessed by measuring the change in the glycated haemoglobin (HbA1c), Fasting Plasma Glucose (FPG), Post Prandial Blood Glucose (PPBH) levels after 12 weeks of treatment. FPG, PPBG and HbA1c levels at baseline and 12 weeks. The primary endpoint was changed in HbA1c levels at 12 weeks as compared to the baseline levels in both groups. The secondary endpoints were changes in FPG, PPBG levels at 12 weeks as compared to baseline levels. Along with, serum cholesterol, triglycerides (TG), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) levels were measured both at baseline and after 12 weeks. Results: At study end, HbA1c levels were reduced from baseline by 0.7% (P = 0.0049) in the pioglitazone group and 1% (P = 0.0002) in the teneligliptin group. The mean changes in FPG levels from baseline to week 12 were ?39.8 mg/dl (P ≤ 0.0001) in teneligliptin and ?11.48 mg/dl (P = 0.00380) in pioglitazone group. The mean PPG levels from ?47.8 mg/dl (P = 0.0003) in teneligliptin and ?25.5 mg/dl (P = 0015) in pioglitazone group. After 12 weeks of study, the levels of TG, total cholesterol (TC), LDL ?71.5 (P = 0.0973), ?15 (P = 0.0501), 18.8 (P ≤ 0.0008) mg/dl and ?31.38 (P ≤ 0.0001), ?21 (P ≤ 0.0001), ?11.68 (P = 0.0028) mg/dl in teneligliptin group and pioglitazone group, respectively. There was significant increase in HDL levels 5.3 (P ≤ 0.0001) mg/dl in teneligliptin group and 5.2 (P = 0.0001) mg/dl in pioglitazone group. Conclusion: Both teneligliptin 20 mg and Pioglitazone 15 mg provided additional HbA1c lowering to that achieved with MF and SU. Teneligliptin showed more effective reductions in HbA1c, FPG, PPBG, HDL and LDL levels. Pioglitazone showed significant changes in HbA1c, HDL, TC, triglyceride levels and significant changes in FPG, PPBG and LDL levels. Reduction in HbA1c and plasma lipids slows down the diabetes progression and decreases the risk of microvascular and macrovascular complications.
机译:目的:该研究的主要目的是比较在二甲双胍(双重治疗)控制不佳的2型糖尿病(T2DM)患者中,替尼格列汀(每天20次)和吡格列酮(每天一次15 mg)联合治疗的疗效MF)加上磺酰脲(SU)。材料与方法:这是一项前瞻性,观察性,比较性研究,对来自印度特兰甘纳邦州Warangal的Sri Bhadrakali医院门诊部的患者进行了研究。在治疗12周后,通过测量糖化血红蛋白(HbA1c),空腹血浆葡萄糖(FPG),餐后血糖(PPBH)水平的变化,评估吡格列酮和替奈格列汀的疗效。基线和12周时的FPG,PPBG和HbA1c水平。与两组的基线水平相比,在12周时主要终点的HbA1c水平发生了变化。次要终点是与基线水平相比在第12周时FPG,PPBG水平的变化。在基线时和第12周后,还测量血清胆固醇,甘油三酸酯(TG),高密度脂蛋白(HDL)和低密度脂蛋白(LDL)的水平。结果:在研究结束时,吡格列酮组的HbA1c水平较基线降低0.7%(P = 0.0049),而替奈格列汀组则降低1%(P = 0.0002)。替奈格列汀从基线到第12周的FPG水平平均变化为?39.8 mg / dl(P≤0.0001),吡格列酮组为?11.48 mg / dl(P = 0.00380)。替格列汀的平均PPG水平从〜47.8 mg / dl(P = 0.0003)和吡格列酮组从〜25.5 mg / dl(P = 0015)。在研究12周后,TG,总胆固醇(TC),LDL的水平分别为71.5(P = 0.0973),15(P = 0.0501),18.8(P≤0.0008)mg / dl和31.38(P≤0.0001) ),替奈格列汀组和吡格列酮组分别为?21(P≤0.0001)、? 11.68(P = 0.0028)mg / dl。替格列汀组的高密度脂蛋白水平显着增加5.3(P≤0.0001)mg / dl,吡格列酮组的HDL水平显着增加5.2(P = 0.0001)mg / dl。结论:teneligliptin 20 mg和Pioglitazone 15 mg均可提供额外的HbA1c降低至MF和SU达到的水平。特立格列汀显示出更有效的降低HbA1c,FPG,PPBG,HDL和LDL水平。吡格列酮显示HbA1c,HDL,TC,甘油三酯水平显着变化,FPG,PPBG和LDL水平显着变化。 HbA1c和血浆脂质的减少减慢了糖尿病的进展,并降低了微血管和大血管并发症的风险。

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