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恩格列净在孟加拉国2型糖尿病患者中的疗效和安全性评估(EFFISAEM研究)

Evaluation of Efficacy and Safety of Empagliflozin in Bangladeshi Patients with Type 2 Diabetes Mellitus (EFFISAEM Study).

作者信息

Saifuddin Mohammad, Paul Ajit K, Shefin Sultana M, Alam Md Jahangir, Selim Shahjada, Islam Sunjida, Hossain Tanjina, Tuqan Sadiqa, Sultana Nusrat, Mustari Marufa, Basak Ramen C, Aftab Kazi A, Prasad Indrajit, Uddin Mohammad R, Sharker Shoma, Gaffar Md Abu Jar, Rahman Mohammad M, Hannan Mohammad A, Ahammed Afsar, Kamrul-Hasan Abm

机构信息

Department of Endocrinology, Dhaka Medical College, Dhaka, Bangladesh.

Department of Endocrinology, Mainamoti Medical College, Cumilla, Bangladesh.

出版信息

Indian J Endocrinol Metab. 2024 Sep-Oct;28(5):500-509. doi: 10.4103/ijem.ijem_189_23. Epub 2024 Mar 8.

Abstract

BACKGROUND

Empagliflozin is a relatively newer glucose-lowering drug (GLD) with many extra-glycemic benefits. To date, no study has evaluated the efficacy and safety of empagliflozin in Bangladeshi patients with type 2 diabetes mellitus (T2DM).

OBJECTIVES

To assess the efficacy and safety of empagliflozin as an add-on to ongoing GLDs in Bangladeshi adults with uncontrolled T2DM.

MATERIALS AND METHODS

This real-world, multicenter, open-label, prospective study was carried out at 21 sites throughout Bangladesh from 1 February 2022 to 31 July 2022. Patients with T2DM who met the criteria had Empagliflozin added to their existing GLD treatment, with necessary modifications to their ongoing medication regimen. The efficacy and safety data were collected 12 weeks after empagliflozin initiation.

RESULTS

Out of 1449 subjects initiating empagliflozin, 1340 subjects [age 50.3 ± 9.0 years, male 52.5%, overweight/obese 94.4%, insulin-treated 25.7%, baseline hemoglobin A1c (Hba1c) 9.9 ± 1.4%] completed the study. At 12 weeks, the reduction in HbA1c was 1.6% (95% CI 1.5-1.6, < 0.001); 12.5% of the study subjects achieved HbA1c < 7%. There were also significant ( < 0.001 in all instances) reductions in fasting plasma glucose (3.0 mmol/L), plasma glucose 2 hours after breakfast (4.8 mmoL/L), body weight (1.9 kg), body mass index (0.8 kg/m), systolic blood pressure (BP) (10 mmHg), diastolic BP (7 mmHg), insulin dose (3 U), serum creatinine (0.06 mg/dL), total cholesterol (18 mg/dL), low-density lipoprotein cholesterol (13 mg/dL), high-density lipoprotein cholesterol (1 mg/dL), and triglyceride (42 mg/dL) and an increase in estimated glomerular filtration rate (4.2 mL/min/1.73 m) from the baseline values. 6.62% experienced adverse events (lightheadedness 2.21%, genital tract infection 0.97%, urinary tract infection 1.24%, generalized weakness 0.48%, and nocturia 0.48%). 1.1% of subjects experienced hypoglycemia, and other 0.12% reported severe hypoglycemic events.

CONCLUSION

Empagliflozin is effective, safe, and tolerable for treating Bangladeshi patients with uncontrolled T2DM as add-on therapy in routine clinical practice with favorable effects on body weight, BP, lipid profile, and renal function.

摘要

背景

恩格列净是一种相对较新的降糖药物(GLD),具有许多血糖外益处。迄今为止,尚无研究评估恩格列净在孟加拉国2型糖尿病(T2DM)患者中的疗效和安全性。

目的

评估恩格列净作为正在使用的降糖药物的附加治疗药物,对孟加拉国未得到有效控制的T2DM成年患者的疗效和安全性。

材料与方法

本项真实世界、多中心、开放标签的前瞻性研究于2022年2月1日至2022年7月31日在孟加拉国各地的21个地点进行。符合标准的T2DM患者在其现有的降糖药物治疗基础上加用恩格列净,并对其正在进行的药物治疗方案进行必要调整。在开始使用恩格列净12周后收集疗效和安全性数据。

结果

在1449名开始使用恩格列净的受试者中,1340名受试者[年龄50.3±9.0岁,男性占52.5%,超重/肥胖者占94.4%,接受胰岛素治疗者占25.7%,基线糖化血红蛋白(Hba1c)为9.9±1.4%]完成了研究。在12周时,糖化血红蛋白降低了1.6%(95%CI 1.5 - 1.6,P<0.001);12.5%的研究受试者糖化血红蛋白<7%。空腹血糖(降低3.0 mmol/L)、早餐后2小时血糖(降低4.8 mmol/L)、体重(降低1.9 kg)、体重指数(降低0.8 kg/m²)、收缩压(降低10 mmHg)、舒张压(降低7 mmHg)、胰岛素剂量(降低3 U)、血清肌酐(降低0.06 mg/dL)、总胆固醇(降低18 mg/dL)、低密度脂蛋白胆固醇(降低13 mg/dL)、高密度脂蛋白胆固醇(升高1 mg/dL)和甘油三酯(降低42 mg/dL)也均有显著降低(所有情况下P<0.001),且估算肾小球滤过率较基线值增加了4.2 mL/min/1.73m²。6.62%的患者发生不良事件(头晕2.21%、生殖道感染0.97%、尿路感染1.24%、全身乏力0.48%、夜尿症0.48%)。1.1%的受试者发生低血糖,另有0.12%报告了严重低血糖事件。

结论

在常规临床实践中,恩格列净作为附加治疗药物治疗孟加拉国未得到有效控制的T2DM患者是有效、安全且可耐受的,对体重、血压、血脂谱和肾功能均有有益影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/186a/11642514/fd44ba6cdfc5/IJEM-28-500-g001.jpg

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