Department of Diabetology and Nephrology, Ogaki Municipal Hospital, Ogaki, Japan.
Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
J Diabetes Investig. 2019 Mar;10(2):392-398. doi: 10.1111/jdi.12877. Epub 2018 Jul 25.
AIMS/INTRODUCTION: Bullous pemphigoid (BP) might be drug-induced. The present study evaluated the relationship between BP and dipeptidyl peptidase-4 inhibitors (DPP4Is).
We recruited patients diagnosed with BP at Ogaki Municipal Hospital from 1 December 2009 through 31 December 2017. We retrospectively collected data from medical records and divided patients into two groups based on whether they received DPP4Is. Additionally, we determined the incidence of BP in patients who were first prescribed DPP4Is at our hospital during the study period.
Of 168 patients diagnosed with BP, 133 (79.1%) were positive for anti-BP180NC16a antibody. A total of 32 (19.0%) patients had been prescribed a DPP4I, 21 of whom (65.6%) were positive for anti-BP180NC16a antibody; this rate was lower than that in patients not receiving a DPP4I (82.3%; P = 0.0360). A total of 16 patients with type 2 diabetes mellitus had not been prescribed a DPP4I; only one (6.3%) was positive for anti-BP180NC16a antibody (P = 0.0339). During the study period, 9,304 patients were prescribed DPP4Is, eight of whom developed BP; six (75.0%) had non-inflammatory BP, and five of the six (83.3%) were negative for anti-BP180NC16a antibody.
The positive rate of anti-BP180NC16a antibody was lower in BP patients with DPP4I than without DPP4I, regardless of type 2 diabetes mellitus. The antibody titer was low in both the overall and type 2 diabetes mellitus populations. The prevalence of BP in 9,304 patients receiving DPP4Is was 0.0859%, which is higher than that in the general population. As DPP4Is are common diabetes treatments, we must be aware of the risk of BP.
目的/引言:大疱性类天疱疮(BP)可能是药物诱导的。本研究评估了 BP 与二肽基肽酶-4 抑制剂(DPP4I)之间的关系。
我们招募了 2009 年 12 月 1 日至 2017 年 12 月 31 日期间在大垣市医院诊断为 BP 的患者。我们从病历中回顾性地收集数据,并根据是否接受 DPP4I 将患者分为两组。此外,我们确定了在研究期间首次在我院开处 DPP4I 的患者中 BP 的发生率。
在 168 名诊断为 BP 的患者中,有 133 名(79.1%)抗 BP180NC16a 抗体阳性。共有 32 名(19.0%)患者接受了 DPP4I 治疗,其中 21 名(65.6%)抗 BP180NC16a 抗体阳性;这一比例低于未接受 DPP4I 治疗的患者(82.3%;P = 0.0360)。共有 16 名 2 型糖尿病患者未服用 DPP4I;其中只有 1 名(6.3%)抗 BP180NC16a 抗体阳性(P = 0.0339)。在研究期间,有 9304 名患者服用了 DPP4I,其中 8 名患者发生了 BP;6 名(75.0%)为非炎症性 BP,其中 6 名中的 5 名(83.3%)抗 BP180NC16a 抗体阴性。
无论是否患有 2 型糖尿病,接受 DPP4I 治疗的 BP 患者的抗 BP180NC16a 抗体阳性率均低于未接受 DPP4I 治疗的患者。总体和 2 型糖尿病患者的抗体滴度均较低。在接受 DPP4I 治疗的 9304 名患者中,BP 的患病率为 0.0859%,高于普通人群。由于 DPP4I 是常见的糖尿病治疗药物,我们必须意识到 BP 的风险。