Shimoda Kenichiro, Hoshino Teruhiko, Morisaki Takafumi, Shiotsu Kazunori, Mizuno Yuji
Department of Pharmacy, Kumamoto Kinoh Hospital.
Division of Cardiovascular Medicine, Kumamoto Kinoh Hospital.
Yakugaku Zasshi. 2018;138(10):1323-1327. doi: 10.1248/yakushi.18-00060.
Incretin-based therapy consists of dipeptidyl peptidase-4 (DPP-4) inhibitors and glucagon-like peptide-1 (GLP-1) receptor agonists. Whether switching from DPP-4 inhibitors to one of the GLP-1 receptor agonists, dulaglutide, has greater beneficial effects remains unknown. Therefore, this study aimed to investigate the effectiveness of switching from DPP-4 inhibitors to dulaglutide in four patients with type 2 diabetes. All four patients with hyperglycemia who switched from DPP-4 inhibitors to dulaglutide demonstrated noticeable decreased plasma glucose levels on the next day after switching. Two of the patients observed maintained a decreased plasma glucose level over 14 day after switching. Moreover, all patients demonstrated decreased glycosylated hemoglobin A1c levels during the observation period (1-6 months) after switching and lost weight from 6 to 27 day. Minor and manageable hypoglycemia, nausea, and diarrhea were observed as side effects in one case. The current findings suggest that dulaglutide is a suitable treatment alternative in patients with type 2 diabetes who are not currently achieving adequate glycemic control with DPP-4 inhibitors.
基于肠促胰岛素的治疗方法包括二肽基肽酶-4(DPP-4)抑制剂和胰高血糖素样肽-1(GLP-1)受体激动剂。从DPP-4抑制剂转换为GLP-1受体激动剂之一度拉糖肽是否具有更大的有益效果尚不清楚。因此,本研究旨在调查4例2型糖尿病患者从DPP-4抑制剂转换为度拉糖肽的有效性。所有4例从DPP-4抑制剂转换为度拉糖肽的高血糖患者在转换后的第二天血糖水平均显著下降。观察到其中2例患者在转换后14天内血糖水平持续下降。此外,所有患者在转换后的观察期(1 - 6个月)内糖化血红蛋白A1c水平均下降,且在6至27天内体重减轻。有1例患者出现轻微且可控的低血糖、恶心和腹泻等副作用。目前的研究结果表明,对于目前使用DPP-4抑制剂未实现充分血糖控制的2型糖尿病患者,度拉糖肽是一种合适的治疗选择。