Exploring factors predicting the effectiveness of oral semaglutide in Japanese individuals with type 2 diabetes switching from dipeptidyl peptidase 4 inhibitors: a pilot study.

Frontiers in clinical diabetes and healthcare Pub Date : 2025-03-24 eCollection Date: 2025-01-01 DOI:10.3389/fcdhc.2025.1520389
Takao Hirotsu, Kanta Taniguchi, Rimei Nishimura
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引用次数: 0

Abstract

Introduction: Oral semaglutide is a glucagon-like peptide-1 receptor agonist (GLP-1 RA) approved for the treatment of type 2 diabetes mellitus (T2DM). Findings from randomized controlled trials (RCTs) and real-world studies indicate that oral semaglutide leads to significant improvements in HbA1c and body weight, comparable to those observed with injectable GLP-1 RAs. Consequently, oral semaglutide is expected to significantly reduce barriers to initiating GLP-1 RA therapy in individuals with diabetes and may lead to an increased transition from dipeptidyl peptidase-4 inhibitors (DPP-4is) to GLP-1 RA therapy. This study was conducted to prospectively investigate the clinical characteristics predicting the achievement of HbA1c < 7% (52 mmol/mol) in Japanese individuals with T2DM who switched from DPP-4is to oral semaglutide.

Methods: The study enrolled a total of 74 patients who switched from DPP-4is to oral semaglutide between December 2021 and October 2022, with the dose being uptitrated to achieve HbA1c < 7% (52 mmol/mol) in these patients.

Results: The study included a total of 44 individuals who achieved the target with oral semaglutide 3 mg (n=7), 7 mg (n=24), or 14 mg (n=13), and 17 individuals who did not (un-achieved group; n=17), based on their clinical characteristics and hematological findings. In the comparison between the Un-achieved group and the Achieved (3 to 14 mg) group, the proportions of "Current alcohol drinking (p = 0.030)" and "Current alcohol drinking and smoking (p = 0.029)" were higher in the Un-achieved group, whereas the proportion of "Taking 31 minutes or longer to have breakfast after drug administration (p = 0.022)" was higher in the Achieved (3 to 14 mg) group. A logistic regression analysis using the stepwise method identified "No current history of both smoking and alcohol drinking (0.083[0.014-0.485]; p = 0.006)" and "Taking 31 minutes or longer to eat breakfast after drug administration (0.117[0.029-0.480]; p = 0.003)" as factors predicting the achievement of the HbA1c < 7% (52 mmol/mol).

Conclusion: Study findings suggest when considering switching T2D patients from DPP-4is to oral semaglutide, a detailed assessment of "current alcohol drinking and smoking status" and "the duration between the administration of oral semaglutide and breakfast" may be useful as a predictive indicator for achieving HbA1c < 7% (52 mmol/mol).

探索预测从二肽基肽酶 4 抑制剂换药的日本 2 型糖尿病患者口服塞马鲁肽疗效的因素:一项试点研究。
口服semaglutide是一种胰高血糖素样肽-1受体激动剂(GLP-1 RA),被批准用于治疗2型糖尿病(T2DM)。随机对照试验(RCTs)和现实世界的研究结果表明,口服semaglutide可显著改善HbA1c和体重,与注射GLP-1 RAs观察到的结果相当。因此,口服semaglutide有望显著降低糖尿病患者启动GLP-1 RA治疗的障碍,并可能导致从二肽基肽酶-4抑制剂(DPP-4is)到GLP-1 RA治疗的过渡增加。本研究旨在前瞻性研究日本T2DM患者从dpp -4转向口服西马鲁肽后,预测HbA1c < 7% (52 mmol/mol)的临床特征。方法:该研究共纳入74名患者,这些患者在2021年12月至2022年10月期间从dpp -4转换为口服西马鲁肽,并增加剂量以使这些患者的HbA1c < 7% (52 mmol/mol)。结果:该研究共包括44名患者,他们分别口服西马鲁肽3mg (n=7)、7mg (n=24)或14mg (n=13),以及17名未达到目标的患者(未达到组;N =17),根据他们的临床特点和血液学表现。未达到组与已达到组(3 ~ 14 mg)比较,未达到组“目前饮酒(p = 0.030)”和“目前饮酒并吸烟(p = 0.029)”的比例较高,而已达到组(3 ~ 14 mg)“服药后早餐时间≥31分钟(p = 0.022)”的比例较高。采用逐步回归方法进行logistic回归分析,确定“当前无吸烟和饮酒史(0.083[0.014-0.485];p = 0.006)和服药后早餐时间≥31分钟(0.117[0.029-0.480];p = 0.003)作为预测实现HbA1c < 7% (52 mmol/mol)的因素。结论:研究结果提示,当考虑将T2D患者从dpp -4转换为口服西马鲁肽时,详细评估“当前饮酒和吸烟状况”以及“口服西马鲁肽与早餐之间的持续时间”可能是实现HbA1c < 7% (52 mmol/mol)的预测指标。
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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