Yamazaki Shunsuke, Takano Tatsuro, Tachibana Koji, Takeda Soichiro, Terauchi Yasuo
Department of Diabetes and Endocrinology, Fujisawa City Hospital, Fujisawa, Japan.
Fujisawa Ekimae Diabetes and Thyroid Clinic, Shotoen Bldg 1F, 600, Fujisawa, Fujisawa-shi, Kanagawa, 251-0052, Japan.
Diabetes Ther. 2022 Aug;13(8):1559-1569. doi: 10.1007/s13300-022-01292-2. Epub 2022 Jul 6.
The combination tablets of dipeptidyl peptidase-4 (DPP-4) inhibitors and metformin are used for both once-daily and twice-daily agents in Japan. If there is no difference in effectiveness between the once-daily and twice-daily DPP-4 inhibitor/metformin combination tablets, the once-daily agent is advantageous in terms of frequency of administration. The aim of this study was to compare the effectiveness of once-daily alogliptin/metformin combination tablet (alogliptin 25 mg/metformin 500 mg) and twice-daily anagliptin/metformin combination tablet low dose (LD) (anagliptin 100 mg/metformin 250 mg).
Forty-eight Japanese patients with type 2 diabetes whose metformin administration of 250 mg twice daily had remained unchanged for at least 8 weeks, except when using DPP-4 inhibitors, glucagon-like peptide-1 receptor agonists, or insulin, were randomized to either the once-daily alogliptin/metformin combination tablet group or the twice-daily anagliptin/metformin combination tablet LD group. The primary endpoint was the difference in glycosylated hemoglobin (HbA1c) levels from baseline to week 12 of administration, whereas the secondary endpoints were fasting blood glucose, body mass index (BMI), and adherence.
Forty-four patients completed the study, and intention-to-treat analyses were performed. The adjusted mean value (standard error) for the change in HbA1c from week 0 to 12, was - 0.75 (0.109)% for the once-daily alogliptin/metformin combination tablet group and - 0.65 (0.109)% for the twice-daily anagliptin/metformin combination tablet LD group, with an intergroup difference of - 0.10% (95% confidence interval, CI - 0.407, 0.215). The upper limit of the bilateral 95% CI was 0.215%, below the 0.40% pre-defined as the non-inferiority margin. Fasting blood glucose, BMI, and adherence were not significantly different between the groups.
The once-daily alogliptin/metformin combination tablet was non-inferior to the twice-daily anagliptin/metformin combination tablet LD in Japanese patients with type 2 diabetes.
University Hospital Medical Information Network Clinical Trial Registry (UMIN-CTR) (registration number: UMIN000034951).
在日本,二肽基肽酶-4(DPP-4)抑制剂与二甲双胍的复方片剂有每日一次和每日两次服用的剂型。如果每日一次和每日两次服用的DPP-4抑制剂/二甲双胍复方片剂在疗效上没有差异,那么每日一次服用的剂型在给药频率方面更具优势。本研究的目的是比较每日一次服用的阿格列汀/二甲双胍复方片剂(阿格列汀25毫克/二甲双胍500毫克)与每日两次服用的阿那格列汀/二甲双胍复方片剂低剂量(LD)(阿那格列汀100毫克/二甲双胍250毫克)的疗效。
48例日本2型糖尿病患者,除使用DPP-4抑制剂、胰高血糖素样肽-1受体激动剂或胰岛素外,二甲双胍每日两次服用250毫克的剂量至少维持8周不变,将其随机分为每日一次服用的阿格列汀/二甲双胍复方片剂组或每日两次服用的阿那格列汀/二甲双胍复方片剂LD组。主要终点是给药第12周糖化血红蛋白(HbA1c)水平相对于基线的变化差异,次要终点是空腹血糖、体重指数(BMI)和依从性。
44例患者完成了研究,并进行了意向性分析。每日一次服用的阿格列汀/二甲双胍复方片剂组从第0周到12周HbA1c变化的调整均值(标准误)为-0.75(0.109)%,每日两次服用的阿那格列汀/二甲双胍复方片剂LD组为-0.65(0.109)%,组间差异为-0.10%(95%置信区间,CI -0.407,0.215)。双侧95%CI的上限为0.215%,低于预先定义为非劣效界值的0.40%。两组间空腹血糖、BMI和依从性无显著差异。
在日本2型糖尿病患者中,每日一次服用的阿格列汀/二甲双胍复方片剂不劣于每日两次服用的阿那格列汀/二甲双胍复方片剂LD。
大学医院医学信息网络临床试验注册中心(UMIN-CTR)(注册号:UMIN000034951)。