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维格列汀在2型糖尿病患者中的心血管安全性和有效性:日本一项为期3年的大规模上市后监测

Cardiovascular safety and effectiveness of vildagliptin in patients with type 2 diabetes mellitus: a 3-year, large-scale post-marketing surveillance in Japan.

作者信息

Ishida Yosuke, Murayama Hiroki, Shinfuku Yohei, Taniguchi Tomoko, Sasajima Takayoshi, Oyama Naotsugu

机构信息

Medical Division, Novartis Pharma K.K, Tokyo, Japan.

Regulatory Office Japan, Novartis Pharma K.K., Tokyo, Japan.

出版信息

Expert Opin Drug Saf. 2020 May;19(5):625-631. doi: 10.1080/14740338.2020.1740679. Epub 2020 Mar 31.

Abstract

: The dipeptidyl peptidase-4 (DPP-4) inhibitor vildagliptin is indicated for type 2 diabetes mellitus (T2DM). However, the long-term safety, effectiveness, and clinical relationship with cardiovascular events of vildagliptin have not been evaluated in Japan.: The authors conducted post-marketing surveillance (PMS) to evaluate the safety and effectiveness of vildagliptin in more than 3000 Japanese T2DM patients for up to 3 years. Main assessments included demographics, major adverse cardiovascular events (MACE), adverse events (AEs), adverse drug reactions (ADRs), and glycated hemoglobin (HbA1c).: In this PMS, 3831 patients (775 sites) were registered in April 2010 - April 2012. The safety analysis population comprised 3769 patients; 2085 patients were aged ≥65 years, and 240, 411, and 114 had renal impairment, hepatic impairment, and heart failure, respectively. The median treatment duration was 2.7 years. The incidence of MACE was 6.04 cases/1000 person-years, mostly attributable to cerebrovascular events (4.27 cases/1000 person-years). The AE and ADR incidences were 26.0% and 5.3%, respectively. The incidence of hypoglycemia was 0.6%. No significant changes in body weight occurred and mean change in HbA1c from baseline at final assessment was -0.74 ± 1.41% ( < 0.0001).: In real-world clinical settings, vildagliptin was well tolerated, with similar profiles as previously reported.

摘要

二肽基肽酶-4(DPP-4)抑制剂维格列汀适用于2型糖尿病(T2DM)。然而,在日本尚未对维格列汀的长期安全性、有效性以及与心血管事件的临床关系进行评估。

作者开展了上市后监测(PMS),以评估维格列汀在3000多名日本T2DM患者中长达3年的安全性和有效性。主要评估指标包括人口统计学数据、主要不良心血管事件(MACE)、不良事件(AE)、药物不良反应(ADR)以及糖化血红蛋白(HbA1c)。

在这项PMS中,2010年4月至2012年4月期间登记了3831例患者(775个地点)。安全性分析人群包括3769例患者;2085例患者年龄≥65岁,分别有240例、411例和114例存在肾功能损害、肝功能损害和心力衰竭。中位治疗持续时间为2.7年。MACE的发生率为6.04例/1000人年,主要归因于脑血管事件(4.27例/1000人年)。AE和ADR的发生率分别为26.0%和5.3%。低血糖的发生率为0.6%。体重无显著变化,最终评估时HbA1c较基线的平均变化为-0.74±1.41%(<0.0001)。

在真实世界的临床环境中,维格列汀耐受性良好,与先前报道的情况相似。

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