Effectiveness of Glipizide and Glipizide Plus Metformin Formulation among Asian Indians with Type 2 Diabetes: a Real-World, Retrospective Electronic Medical Record Analysis.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY
Thyparambil Aravindakshan PramodKumar, Rajendra Pradeepa, Saravanan Jebarani, Sadasivam Ganesan, Abhijit Pednekar, Routray Philips, Suraparaju Pavan Kumar, Ranjit Unnikrishnan, Ranjit Mohan Anjana, Viswanathan Mohan
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引用次数: 0

Abstract

Background: In low- and middle-income countries, sulfonylureas are commonly prescribed due to cost-effectiveness. However, data comparing their real-world impact, especially when used alone versus in combination with metformin, remain limited.

Objective: This study aimed to assess the effectiveness of glipizide and glipizide plus metformin in individuals with type 2 diabetes (T2D) using real-world data.

Methods: Data was obtained from 11,949 individuals with T2D who were prescribed either glipizide or glipizide+metformin and had at least one follow-up within 1 year at a tertiary diabetes care centre in India. The primary outcome was the change in glycated hemoglobin (HbA1c) levels from baseline to follow-up. Secondary outcomes included changes in fasting plasma glucose (FPG), postprandial glucose (PPG), body mass index (BMI), and estimated glomerular filtration rate (eGFR).

Results: The mean age of participants was 56 ± 11 years, 59% (n = 7008) were male, and the mean diabetes duration was 10.2 ± 8 years. In the glipizide group (n = 6034), HbA1c decreased from 8.8% to 7.9% (p < 0.001), FPG decreased by 16 mg/dL (p < 0.001), and PPG decreased by 29 mg/dL (p < 0.001). In the glipizide + metformin group (n = 5915), HbA1c levels declined from 8.9% to 7.8% (p < 0.001), and FPG and PPG declined by 23 mg/dL and 44 mg/dL, respectively (p < 0.001). BMI remained stable in the glipizide group, while a reduction of 0.2 kg/m2 was observed among overweight/obese individuals in the glipizide + metformin group. The use of glipizide and glipizide + metformin effectively improved glycemic control without adverse anthropometric changes. C-peptide levels were preserved across all treatment groups, demonstrating sustained β-cell function. HbA1c reductions were observed consistently across all eGFR categories. Furthermore, as glipizide plus metformin is one of the least expensive antidiabetic drugs in India (₹1460/year [$16.87]) it can help improve accessibility to treatment even among those in lower socio-economic statuses.

Conclusions: Glipizide as monotherapy or in combination with metformin, significantly improved glycemic control even in those with decreasing renal function, with no adverse effects on weight and with preservation of β-cell function. While long-term studies are needed to assess the sustainability of these benefits, glipizide can be considered a cost-effective therapeutic option for T2D in low- and middle-income countries.

格列吡嗪和格列吡嗪加二甲双胍治疗2型糖尿病的有效性:一项真实世界的回顾性电子病历分析
背景:在低收入和中等收入国家,出于成本效益考虑,通常开具磺脲类药物。然而,比较它们的实际影响的数据,特别是单独使用和与二甲双胍联合使用的数据仍然有限。目的:本研究旨在利用真实数据评估格列吡嗪和格列吡嗪联合二甲双胍治疗2型糖尿病(T2D)的有效性。方法:数据来自11,949例T2D患者,这些患者在印度三级糖尿病护理中心服用格列吡嗪或格列吡嗪+二甲双胍,并在1年内至少进行一次随访。主要结局是糖化血红蛋白(HbA1c)水平从基线到随访的变化。次要结局包括空腹血糖(FPG)、餐后血糖(PPG)、体重指数(BMI)和肾小球滤过率(eGFR)的变化。结果:参与者的平均年龄为56±11岁,59% (n = 7008)为男性,平均糖尿病病程为10.2±8年。在格列吡嗪组(n = 6034), HbA1c从8.8%下降到7.9% (p < 0.001), FPG下降了16 mg/dL (p < 0.001), PPG下降了29 mg/dL (p < 0.001)。在格列吡嗪+二甲双胍组(n = 5915), HbA1c水平从8.9%下降到7.8% (p < 0.001), FPG和PPG分别下降了23 mg/dL和44 mg/dL (p < 0.001)。格列吡嗪组BMI保持稳定,而格列吡嗪+二甲双胍组超重/肥胖个体BMI下降0.2 kg/m2。使用格列吡嗪及格列吡嗪+二甲双胍可有效改善血糖控制,且无不良的人体测量变化。c肽水平在所有治疗组均保持不变,表明β细胞功能持续。在所有eGFR类别中均观察到一致的HbA1c降低。此外,由于格列吡嗪加二甲双胍是印度最便宜的降糖药之一(1460卢比/年[16.87美元]),它可以帮助改善社会经济地位较低的人获得治疗的机会。结论:格列吡嗪单药或联用二甲双胍可显著改善肾功能下降患者的血糖控制,对体重无不良影响,并可保留β细胞功能。虽然需要长期研究来评估这些益处的可持续性,但在低收入和中等收入国家,格列吡嗪可被认为是T2D的一种具有成本效益的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drugs - Real World Outcomes
Drugs - Real World Outcomes PHARMACOLOGY & PHARMACY-
CiteScore
3.60
自引率
5.00%
发文量
49
审稿时长
8 weeks
期刊介绍: Drugs - Real World Outcomes targets original research and definitive reviews regarding the use of real-world data to evaluate health outcomes and inform healthcare decision-making on drugs, devices and other interventions in clinical practice. The journal includes, but is not limited to, the following research areas: Using registries/databases/health records and other non-selected observational datasets to investigate: drug use and treatment outcomes prescription patterns drug safety signals adherence to treatment guidelines benefit : risk profiles comparative effectiveness economic analyses including cost-of-illness Data-driven research methodologies, including the capture, curation, search, sharing, analysis and interpretation of ‘big data’ Techniques and approaches to optimise real-world modelling.
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