Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Canada.
Department of Medicine, McGill University, Montreal, Canada.
Diabetes Care. 2019 Aug;42(8):1496-1503. doi: 10.2337/dc19-0409. Epub 2019 Jun 10.
There are uncertainties regarding the association between dipeptidyl peptidase 4 (DPP-4) inhibitors and bullous pemphigoid (BP), a potentially severe autoimmune skin disease. Thus, we conducted a population-based study to determine whether use of DPP-4 inhibitors, when compared with other second- to third-line antidiabetic drugs, is associated with an increased risk of BP in patients with type 2 diabetes.
Using the U.K. Clinical Practice Research Datalink, we conducted a cohort study among 168,774 patients initiating antidiabetic drugs between January 2007 and March 2018. Using time-dependent Cox proportional hazards models, we estimated adjusted hazard ratios (HRs) with 95% CIs of incident BP associated with current use of DPP-4 inhibitors, compared with current use of other second- to third-line antidiabetic drugs. We also conducted a propensity score-matched analysis to assess the impact of residual confounding.
During 711,311 person-years of follow-up, 150 patients were newly diagnosed with BP (crude incidence rate, 21.1 per 100,000 person-years). Current use of DPP-4 inhibitors was associated with an increased risk of BP (47.3 vs. 20.0 per 100,000 person-years; HR 2.21 [95% CI 1.45-3.38]). HRs gradually increased with longer durations of use, reaching a peak after 20 months (HR 3.60 [95% CI 2.11-6.16]). Similar results were obtained in the propensity score-matched analysis (HR 2.40 [95% CI 1.13-4.66]).
In this large population-based study, use of DPP-4 inhibitors was associated with an at least doubling of the risk of BP in patients with type 2 diabetes, albeit the absolute risk was low.
二肽基肽酶 4(DPP-4)抑制剂与大疱性类天疱疮(BP)之间的关联存在不确定性,BP 是一种潜在严重的自身免疫性皮肤病。因此,我们进行了一项基于人群的研究,以确定与其他二线至三线抗糖尿病药物相比,使用 DPP-4 抑制剂是否会增加 2 型糖尿病患者患 BP 的风险。
利用英国临床实践研究数据链,我们在 2007 年 1 月至 2018 年 3 月期间,对 168774 名开始使用抗糖尿病药物的患者进行了队列研究。使用时间依赖性 Cox 比例风险模型,我们估计了当前使用 DPP-4 抑制剂与当前使用其他二线至三线抗糖尿病药物相比,与 BP 相关的发生率(HR)及其 95%CI。我们还进行了倾向评分匹配分析,以评估残余混杂的影响。
在 711311 人年的随访期间,有 150 名患者新诊断出患有 BP(粗发病率为 21.1/100000 人年)。当前使用 DPP-4 抑制剂与 BP 风险增加相关(47.3 比 20.0/100000 人年;HR 2.21 [95%CI 1.45-3.38])。HR 随使用时间的延长而逐渐增加,在 20 个月后达到峰值(HR 3.60 [95%CI 2.11-6.16])。在倾向评分匹配分析中也得到了类似的结果(HR 2.40 [95%CI 1.13-4.66])。
在这项大型基于人群的研究中,使用 DPP-4 抑制剂与 2 型糖尿病患者 BP 风险增加至少两倍相关,尽管绝对风险较低。