Hayakawa Tetsuo, Kato Ken-Ichiro, Kobuchi Shinji, Kataoka Kaede, Sakaeda Toshiyuki
Department of Diabetes Mellitus and Endocrinology, Tonami General Hospital, Toyama 939-1395, Japan.
Department Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Pharmaceuticals (Basel). 2022 Feb 7;15(2):203. doi: 10.3390/ph15020203.
This study was conducted to evaluate the long-term plasma concentration profiles of dapagliflozin and its effects on the glycated hemoglobin (HbA1c) level, body weight, and estimated glomerular filtration rate (eGFR) in 72 Japanese outpatients with type 2 diabetes mellitus (T2DM) receiving metformin and a dipeptidyl peptidase-4 inhibitor. At baseline, HbA1c level, body weight, and eGFR were 6.9 ± 0.6%, 77.9 ± 13.5 kg, and 78.8 ± 20.7 mL/min/1.73 m, respectively. A once-daily oral dose of 5 mg dapagliflozin was administered, and its trough plasma concentrations were evaluated at 1, 3, 6, 9, and 12 months. In this study, the patients with stable dapagliflozin concentrations were defined, based on a well-organized clinical trial, as those with average plasma concentrations of 2-5 ng/mL with a coefficient of variation <30%; these values were achieved if patients complied with their once-daily dosage. Multivariate analysis showed a significant decrease in the HbA1c levels among patients with stable concentrations (-0.6 ± 0.4%, < 0.01), which was greater than the mean change among all 72 patients (-0.2 ± 0.5%, < 0.01). The patients' mean body weight also decreased (-2.3 ± 4.0 kg, = 0.060). Average plasma concentrations ranged from 1.6 to 11.8 ng/mL; however, multivariate analysis indicated it was unrelated to the HbA1c-lowering effect. In conclusion, the long-term stability of plasma dapagliflozin concentration was important in lowering HbA1c level, and a once-daily oral dose of 5 mg was sufficient in achieving this effect.
本研究旨在评估达格列净在72例接受二甲双胍和二肽基肽酶-4抑制剂治疗的日本2型糖尿病(T2DM)门诊患者中的长期血浆浓度曲线及其对糖化血红蛋白(HbA1c)水平、体重和估算肾小球滤过率(eGFR)的影响。基线时,HbA1c水平、体重和eGFR分别为6.9±0.6%、77.9±13.5 kg和78.8±20.7 mL/min/1.73 m²。给予每日一次口服5 mg达格列净,并在1、3、6、9和12个月时评估其谷浓度。在本研究中,根据一项精心组织的临床试验,将达格列净浓度稳定的患者定义为平均血浆浓度为2 - 5 ng/mL且变异系数<30%的患者;如果患者遵守每日一次的剂量,即可达到这些值。多变量分析显示,浓度稳定的患者HbA1c水平显著降低(-0.6±0.4%,P<0.01),这大于所有72例患者的平均变化(-0.2±0.5%,P<0.01)。患者的平均体重也有所下降(-2.3±4.0 kg,P = 0.060)。平均血浆浓度范围为1.6至11.8 ng/mL;然而,多变量分析表明其与HbA1c降低效果无关。总之,血浆达格列净浓度的长期稳定性对降低HbA1c水平很重要,每日一次口服5 mg足以达到此效果。