Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Clinical Development and Medical Affairs, Nippon Boehringer Ingelheim Co., Ltd, Tokyo, Japan.
Diabetes Obes Metab. 2018 Dec;20(12):2830-2839. doi: 10.1111/dom.13463. Epub 2018 Aug 2.
To evaluate the persistence with oral antidiabetic drug (OAD) treatment characterized by drug class, patient characteristics and severity of renal impairment (RI) in patients with type 2 diabetes (T2DM) in Japan.
This retrospective, observational study extracted data from a large-scale hospital database (April 2008 to September 2016). Patients with T2DM aged ≥40 years on the day of their first prescription (index date) of any OAD (biguanides [BGs], thiazolidinediones [TZDs], sulphonylureas [SUs], glinides, dipeptidyl peptidase-4 [DPP-4] inhibitors, or α-glucosidase inhibitors [α-GIs]) available between January 1, 2014 and September 30, 2016 were identified. Sodium-glucose co-transporter-2 inhibitors were not available at study initiation. Treatment persistence was assessed by Kaplan-Meier survival curves. Patients were also categorized by RI status using estimated glomerular filtration rate: ≥90 mL/min/1.73 m (G1); 60 to <90 mL/min/1.73 m (G2); 30 to <60 mL/min/1.73 m (G3); and <30 mL/min/1.73 m (G4+).
We identified 206 406 index dates from 162 116 eligible patients. The largest number of index dates (91634) was observed for DPP-4 inhibitors, followed by BGs, SUs, α-GIs, glinides and TZDs. Treatment persistence was longest for DPP-4 inhibitors (median 17.0 months, 95% confidence interval [CI] 16.4-17.5) and BGs (median 17.3 months, 95% CI 16.6-18.2), and shortest for α-GIs (median 5.6 months, 95% CI 5.4-5.9) and SUs (median 4.3 months, 95% CI 4.2-4.6). Persistence was longest with DPP-4 inhibitors at all RI stages (G1-G4+), followed by BGs at stages G1/G2.
The longest OAD persistence was observed for BGs and DPP-4 inhibitors at RI stages G1/G2, and for DPP-4 inhibitors at RI stages G3/G4+.
评估日本 2 型糖尿病(T2DM)患者中按药物类别、患者特征和肾功能损害(RI)严重程度划分的口服降糖药(OAD)治疗的持久性。
这是一项回顾性、观察性研究,从一个大型医院数据库中提取数据(2008 年 4 月至 2016 年 9 月)。在 2014 年 1 月 1 日至 2016 年 9 月 30 日期间,将在任何 OAD(二甲双胍[BGs]、噻唑烷二酮[TZDs]、磺酰脲类[SUs]、格列奈类、二肽基肽酶-4[DPP-4]抑制剂或α-葡萄糖苷酶抑制剂[α-GIs])首次处方(索引日期)之日年龄≥40 岁的 T2DM 患者纳入研究。研究开始时,钠-葡萄糖协同转运蛋白 2 抑制剂不可用。通过 Kaplan-Meier 生存曲线评估治疗的持久性。还根据估计肾小球滤过率(eGFR)将患者分为 RI 状态:≥90mL/min/1.73m(G1);60 至<90mL/min/1.73m(G2);30 至<60mL/min/1.73m(G3);和<30mL/min/1.73m(G4+)。
我们从 162116 名合格患者中确定了 206406 个索引日期。DPP-4 抑制剂的索引日期最多(91634 个),其次是 BGs、SUs、α-GIs、格列奈类和 TZDs。DPP-4 抑制剂(中位 17.0 个月,95%置信区间 [CI] 16.4-17.5)和 BGs(中位 17.3 个月,95% CI 16.6-18.2)的治疗持久性最长,而α-GIs(中位 5.6 个月,95% CI 5.4-5.9)和 SUs(中位 4.3 个月,95% CI 4.2-4.6)的治疗持久性最短。在所有 RI 阶段(G1-G4+),DPP-4 抑制剂的持久性最长,其次是 BGs 在 RI 阶段 G1/G2。
在 RI 阶段 G1/G2,BGs 和 DPP-4 抑制剂的 OAD 持久性最长,在 RI 阶段 G3/G4+,DPP-4 抑制剂的 OAD 持久性最长。