Effect of Add-On Therapy of Dapagliflozin and Empagliflozin on Adipokines in Type 2 Diabetes Mellitus

IF 0.6 Q4 ENDOCRINOLOGY & METABOLISM Journal of Endocrinology and Metabolism Pub Date : 2021-07-25 DOI:10.14740/jem751
A. Shaheer, Ashok Kumar, P. Menon, M. Jallo, S. Basha
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引用次数: 1

Abstract

Background: The alteration of adipokine secretion leads to the development of insulin resistance or impaired function of insulin in type 2 diabetes with obesity. The main objective of the study was to evaluate the effect of add-on therapy of dapagliflozin and empagliflozin on visceral fat-associated adipokines in inadequately controlled overweight and obese type 2 diabetic patients on metformin monotherapy. Methods: The study included 60 participants diagnosed with type 2 diabetes mellitus with overweight or obesity. The blood samples were taken before starting first-line therapy with metformin, 12 weeks after starting metformin therapy and 12 weeks after starting add-on therapy. The biochemical variables were analyzed using Cobas ® 6000 analyzer. Hemoglobin A1c (HbA1c) level was measured with high-performance liquid chromatography (HPLC). Serum adipokines were estimated with enzyme-linked immunosorbent assay (ELISA). Results: The mean adiponectin level was significantly elevated with add-on therapy using dapagliflozin and empagliflozin (P < 0.001). The mean fatty-acid binding protein 4 (FABP4), retinol-binding protein 4 (RBP4) and visfatin levels were reduced considerably (P < 0.001). The mean HbA1c, fasting plasma glucose (FPG) and postprandial blood glucose (PPBG) levels were reduced significantly with add-on therapy (P < 0.001). Lipid profile and creatinine were also altered significantly with the add-on therapy (P < 0.001). Conclusions: Add-on therapy of dapagliflozin and empagliflozin are beneficial to control the adipokines that regulate the visceral fat in overweight and obese type 2 diabetic patients. The effective therapeutic target to control adipokines with metabolic variables reduces body weight, obesity, cardiovascular risk and renal disease in type 2 diabetes. J Endocrinol Metab. 2021;11(3-4):83-90 doi: https://doi.org/10.14740/jem751
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达格列嗪和恩帕列嗪联合治疗对2型糖尿病脂蛋白的影响
背景:肥胖的2型糖尿病患者,脂肪因子分泌的改变会导致胰岛素抵抗或胰岛素功能受损。本研究的主要目的是评估达格列嗪和恩帕列嗪联合治疗对二甲双胍单药治疗的超重和肥胖2型糖尿病患者内脏脂肪相关脂肪因子的影响。方法:该研究包括60名被诊断为2型糖尿病并超重或肥胖的参与者。在开始二甲双胍一线治疗前、开始二甲双胍治疗12周后和开始附加治疗12周前采集血样。使用Cobas®6000分析仪对生化变量进行分析。用高效液相色谱法(HPLC)测定血红蛋白A1c(HbA1c)水平。用酶联免疫吸附试验(ELISA)测定血清脂肪因子。结果:达格列嗪和恩帕列嗪联合治疗后,平均脂联素水平显著升高(P<0.001)。平均脂肪酸结合蛋白4(FABP4)、视黄醇结合蛋白4和内脂蛋白水平显著降低(P<0.01),添加治疗可显著降低空腹血糖(FPG)和餐后血糖(PPBG)水平(P<0.001)。添加治疗可明显改变血脂和肌酸酐(P<0.01)糖尿病患者。通过代谢变量控制脂肪因子的有效治疗靶点可以降低2型糖尿病患者的体重、肥胖、心血管风险和肾脏疾病。内分泌代谢杂志。2021年;11(3-4):83-90 doi:https://doi.org/10.14740/jem751
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来源期刊
Journal of Endocrinology and Metabolism
Journal of Endocrinology and Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
0.70
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发文量
21
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