Department of Biochemistry, All India Institute of Medical Sciences, Rajkot, India.
Department of Pharmacology, All India Institute of Medical Sciences, Rajkot, India.
Expert Opin Pharmacother. 2023 Sep-Dec;24(18):2187-2198. doi: 10.1080/14656566.2023.2269854. Epub 2024 Jan 5.
This study assessed the clinical safety and efficacy of bexagliflozin, a sodium-glucose cotransporter 2(SGLT2) inhibitor, in managing glycemia among patients with type 2 diabetes mellitus (T2DM).
We examined RCTs with T2DM comparing the clinical effectiveness and safety of 20 mg once daily oral dose of bexagliflozin with placebo for managing glycemia till 28 May 2023, published on databases like ClinicalTrials.gov, PubMed, Embase, and Cochrane Library. Furthermore, reduction of body weight, fasting plasma sugarr(FPG), systolic blood pressure (SBP) and the percentage of individuals who achieved glycated hemoglobin (HbA1c) of < 7% from baseline were also evaluated. The Review Manager 5 was utilized to investigate the retrieved data.
We involved eight RCTs. Bexagliflozin was significantly superior in reducing HbA1c[least squares mean difference(LSMD) = -0.45,95% confidence interval (CI =-0.55 to -0.34, < 0.00001], FPG [LSMD= -1.37, 95%CI =-1.73 to -1.00, < 0.00001], body weight (LSMD= -1.77, 95%CI =-2.44 to-1.10, < 0.00001), and SBP(LSMD= -4.11,95%CI = -6.18 to -2.03, = 0.0001) in comparison to placebo. The safety outcomes of bexagliflozin were consistent with the placebo arm. This study concluded that bexagliflozin seems to be a promising oral anti-diabetic drug for enhancing glycemic management in adult patients with T2DM.
本研究评估了钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂贝格列净在 2 型糖尿病(T2DM)患者血糖管理中的临床安全性和疗效。
我们检索了截止 2023 年 5 月 28 日在 ClinicalTrials.gov、PubMed、Embase 和 Cochrane Library 等数据库中发表的比较 20mg 每日一次口服贝格列净与安慰剂治疗 T2DM 的 RCTs,评估了临床疗效和安全性。此外,还评估了体重减轻、空腹血糖(FPG)、收缩压(SBP)和达到糖化血红蛋白(HbA1c)<7%的个体比例从基线的变化。使用 Review Manager 5 分析检索到的数据。
我们纳入了八项 RCT。贝格列净在降低 HbA1c[最小二乘均数差值(LSMD)=-0.45,95%置信区间(CI)=-0.55 至-0.34,<0.00001]、FPG[LSMD=-1.37,95%CI=-1.73 至-1.00,<0.00001]、体重(LSMD=-1.77,95%CI=-2.44 至-1.10,<0.00001)和 SBP(LSMD=-4.11,95%CI=-6.18 至-2.03,=0.0001)方面明显优于安慰剂。贝格列净的安全性结局与安慰剂组一致。本研究得出结论,贝格列净似乎是一种有前途的口服抗糖尿病药物,可改善 T2DM 成年患者的血糖管理。