使用连续血糖监测的固定剂量达格列净和西格列汀联合治疗2型糖尿病的疗效:印度的一项真实世界研究

S. Bhattacharyya, Sameer Muchhala, Kunal Jhaveri
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引用次数: 0

摘要

背景:2型糖尿病(T2DM)是一种多因素的进行性疾病。二甲双胍单药治疗通常作为初始治疗,但往往不足以达到最佳的血糖控制,需要二线和三线治疗。达格列净和西格列汀的固定剂量联用在印度越来越流行。目标时间已成为一个有用的血糖指标,“超越糖化血红蛋白”,以更好地了解糖尿病患者的血糖控制。目的和目的:评估达格列净和西格列汀在印度T2DM患者中的FDC疗效。材料和方法:这是一项单臂、单中心、真实世界的研究。28名年龄>18岁、未住院且肾小球滤过率>60 ml/min/1.73m2的T2DM患者接受了连续血糖监测系统(Freestyle Libre Pro)。在现有的治疗背景下,对那些不以血糖参数为目标的患者给予每日一次的达格列净(10mg)和西格列汀(100mg)的固定剂量联合用药(FDC)和CGMS。由于FDC在给药3-4天后浓度达到峰值,所以从第5天开始考虑FDC的疗效。因此,以FDC给药后头4天的平均值计算基线。记录患者的特征,包括年龄(岁)、性别、体重(kg)、体重指数(kg/m2)、估计糖化血红蛋白(%)、口服降糖药史和胰岛素剂量。为了评估疗效,在基线和研究结束时(给药第15天)记录自由式Libre Pro CGMS每日葡萄糖总结的平均每日葡萄糖(ADG)、达到目标时间(TIT)、低于目标时间(TBT)和高于目标时间(TAT)。评估各疗效指标的改善百分比。结果:ADG(降低19.41%)、TIT(提高34.47%)、TAT(降低31.13%)改善有统计学意义(p<0.05), TBT提高29.23%。平均年龄(n=28)、体重(n=23)、体重指数(n=19)和估计HbA1c (n=19)分别为56.70±9.8岁、64.67±9.52 Kg、24.99±4.23 Kg/m2和6.84±1.63%。多数为三联用药(n=14;50%)在CGMS给药前治疗比双重治疗(n=5;17.9%)和单药治疗(2;7.1%)。15例(53.8%)使用胰岛素,平均胰岛素剂量为16.40 IU。结论:印度T2DM患者每日1次口服达格列净和西格列汀可显著改善15 d时的AGD、TIT和TAT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Fixed-dose Combination of Dapagliflozin and Sitagliptin in Type 2 Diabetes Mellitus Using Continuous Glucose Monitoring: A Real-world Study in India
Background: Type 2 diabetes mellitus (T2DM) is a progressive disease with multifactorial aetiology. Metformin monotherapy is commonly used as the initial treatment, but is often inadequate in achieving optimal glycaemic control, necessitating the need of second and third-line therapies. Fixed dose combination (FDC) of dapagliflozin and sitagliptin in Indian setting is gaining popularity. Time-in-target has become a useful blood glucose indicator that goes "beyond HbA1c" to understand glycaemic control in people with diabetes better. Aims and Objectives: To assess the efficacy of a FDC of dapagliflozin and sitagliptin in Indian T2DM patients. Materials and Methods: This was a single-arm, single-centre, real-world study. Twenty-eight consented T2DM patients age >18 years, either sex, not hospitalized, and estimated glomerular filtration rate >60 ml/min/1.73m2 were administered a continuous glucose monitoring system (CGMS) (Freestyle Libre Pro). Once daily fixed-dose combination (FDC) of dapagliflozin (10mg) and sitagliptin (100mg) was given along with CGMS administration on a background of existing therapy for those who were not to target for glycemic parameters. Since the FDC reaches at its peak concentration after 3-4 days of administration, the efficacy of FDC was considered from 5th day. Hence the baseline was calculated taking the mean of first 4 days after FDC administration. Patients' characteristics, including age (years), sex, weight (kg), body mass index (kg/m2), estimated glycated haemoglobin (%), history of oral hypoglycaemic agents, and dose of insulin were recorded. For efficacy assessment, average daily glucose (ADG), time in target (TIT), time below target (TBT), and time above target (TAT) were recorded at baseline.) and end of the study (day 15th of CGMS administration) from the daily glucose summary of Freestyle Libre Pro CGMS. The percentage improvement of each efficacy parameters were assessed. Results: A statistically significant improvement (p<0.05) in ADG (19.41% decrease), TIT (34.47% increase), and TAT (31.13% decrease) was observed, whereas TBT was increased by 29.23%. Mean age (n=28), weight (n=23), body mass index (n=19) and estimated HbA1c (n=19) was 56.70±9.8 years, 64.67±9.52 Kg, 24.99±4.23 Kg/m2 and 6.84±1.63 % respectively. The majority were on triple drug (n=14; 50%) therapy before CGMS administration than dual (n=5; 17.9%) and monotherapy (2; 7.1%). Fifteen (53.8%) were on insulin with a mean insulin dose of 16.40 IU. Conclusion: Once daily FDC of dapagliflozin and sitagliptin in Indian T2DM patients significantly improves AGD, TIT, and TAT at the end of 15 days.
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