Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Division of Anticipatory Molecular Food Science and Technology, Medical Research Institute, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
J Diabetes Investig. 2019 May;10(3):706-713. doi: 10.1111/jdi.12917. Epub 2018 Oct 1.
AIMS/INTRODUCTION: The objective of the present study was to elucidate the effect of switching to teneligliptin from other dipeptidyl peptidase-4 (DPP-4) inhibitors on glucose control and renoprotection in type 2 diabetes mellitus patients with diabetic kidney disease.
The present study was a single-arm, open-label, observational study. A total of 23 patients, who had urinary albumin/creatinine ratios (UACR) ≥30 mg/gCr in their first urine in the early morning, and received other DPP-4 inhibitors and renin-angiotensin system inhibitors, switched to teneligliptin 20 mg/day. After switching to teneligliptin for 24 weeks, we evaluated changes in glycated hemoglobin (HbA1c), fasting plasma glucose levels, plasma DPP-4 activity and UACR.
HbA1c, fasting plasma glucose and UACR values showed no significant change after 24 weeks compared with baseline. However, plasma DPP-4 activity was significantly reduced after 24 weeks (0.57 ± 0.26 nmol/min/mL, P = 0.012, vs baseline), compared with baseline (1.49 ± 1.73 nmol/min/mL), and there was a positive relationship between the change rate of plasma DPP-4 activity (Δ%DPP-4) for 24 weeks and the levels of plasma DPP-4 activity (r = -0.5997, P = 0.0025) and fasting plasma glucose (r = -0.4235, P = 0.0440) at baseline. Additionally, the Δ%DPP-4 for 24 weeks was significantly correlated to the change rate of UACR (r = 0.556, P = 0.0059). However, there was no relationship between Δ%DPP-4 and ΔHbA1c (amount of HbA1c change).
Switching to teneligliptin from other DPP-4 inhibitors for 24 weeks reduces plasma DPP-4 activity, which is associated with a reduction in albuminuria, independent of the change in glucose levels, in type 2 diabetes mellitus patients with diabetic kidney disease.
目的/引言:本研究的目的在于阐明 2 型糖尿病合并糖尿病肾病患者由其他二肽基肽酶-4(DPP-4)抑制剂转换为替格列汀后对血糖控制和肾脏保护的影响。
本研究为单臂、开放标签、观察性研究。共 23 例患者,晨尿中尿白蛋白/肌酐比值(UACR)≥30mg/gCr,且接受其他 DPP-4 抑制剂和肾素-血管紧张素系统抑制剂治疗,转换为替格列汀 20mg/天。转换为替格列汀治疗 24 周后,评估糖化血红蛋白(HbA1c)、空腹血糖水平、血浆 DPP-4 活性和 UACR 的变化。
与基线相比,24 周时 HbA1c、空腹血糖和 UACR 无显著变化。然而,与基线相比(1.49±1.73nmol/min/mL,P=0.012),24 周时血浆 DPP-4 活性显著降低(0.57±0.26nmol/min/mL),并且血浆 DPP-4 活性的变化率(Δ%DPP-4)与基线时的血浆 DPP-4 活性(r=-0.5997,P=0.0025)和空腹血糖(r=-0.4235,P=0.0440)呈正相关。此外,24 周时的Δ%DPP-4与 UACR 的变化率(r=0.556,P=0.0059)显著相关。然而,Δ%DPP-4 与ΔHbA1c(HbA1c 变化量)之间无相关性。
2 型糖尿病合并糖尿病肾病患者由其他 DPP-4 抑制剂转换为替格列汀治疗 24 周可降低血浆 DPP-4 活性,与血糖水平变化无关,可降低白蛋白尿。