Department of Pharmacy, New Taipei Municipal TuCheng Hospital (Built and Operated by Chang Gung Medical Foundation), New Taipei City, Taiwan.
Department of Dermatology, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan.
JAMA Dermatol. 2020 Aug 1;156(8):891-900. doi: 10.1001/jamadermatol.2020.1587.
The association between the use of medications and the development of bullous pemphigoid (BP) is unclear.
To assess the associations between previous exposure to certain medications and BP.
For this systematic review and meta-analysis, PubMed, the Cochrane Central Register of Controlled Trials, and Embase were searched for relevant studies from inception to February 20, 2020.
Case-control or cohort studies and randomized clinical trials that examined the odds or risk of BP in patients with previous medication use were included. No geographic or language limitations were imposed.
The Meta-analysis of Observational Studies in Epidemiology (MOOSE) guideline was followed. The Newcastle-Ottawa Scale was used to evaluate the risk of bias of included observational studies; Cochrane Collaboration's tool was used for randomized clinical trials. Aggregate data were used to conduct a random-effects model meta-analysis if the included studies were sufficiently homogenous. Subgroup analyses were performed for use of various medications of the same category.
Odds ratio (OR), hazard ratio, and risk ratio of bullous pemphigoid in association with medication use.
This meta-analysis included 13 case-control studies, 1 cohort study, and 1 randomized clinical trial with a total of 285 884 participants. The meta-analysis of case-control studies showed a significant association of BP with previous use of aldosterone antagonists (pooled OR, 1.75; 95% CI, 1.28-2.40), dipeptidyl peptidase 4 inhibitors (pooled OR, 1.92; 95% CI, 1.55-2.38), anticholinergics (pooled OR, 3.12; 95% CI, 1.54-6.33), and dopaminergic medications (pooled OR, 2.03; 95% CI, 1.34-3.05). One cohort study found an increased risk of BP among patients receiving dipeptidyl peptidase 4 inhibitors (hazard ratio, 2.38; 95% CI, 1.16-4.88; P = .02). One trial found a higher occurrence of BP in patients with diabetes receiving linagliptin (0.2% in diabetes group vs 0% in the placebo group).
The findings of this systematic review and meta-analysis suggest that aldosterone antagonists, dipeptidyl peptidase 4 inhibitors, anticholinergics, and dopaminergic medications are associated with BP. These medications should be judiciously prescribed, particularly in high-risk patients who are elderly and have disabling neurologic disorders.
药物使用与大疱性类天疱疮(BP)的发展之间的关联尚不清楚。
评估先前暴露于某些药物与 BP 之间的关联。
本系统评价和荟萃分析检索了从成立到 2020 年 2 月 20 日的 PubMed、Cochrane 对照试验中心注册库和 Embase 相关研究。
纳入了病例对照或队列研究以及随机临床试验,以检查先前使用药物的患者中 BP 的几率或风险。没有对地理或语言进行限制。
遵循观察性研究的荟萃分析(MOOSE)指南。使用纽卡斯尔-渥太华量表评估纳入观察性研究的偏倚风险;Cochrane 协作工具用于随机临床试验。如果纳入研究足够同质,则使用汇总数据进行随机效应模型荟萃分析。对同一类别药物的使用进行了亚组分析。
与药物使用相关的大疱性类天疱疮的比值比(OR)、风险比和危险比。
这项荟萃分析包括 13 项病例对照研究、1 项队列研究和 1 项随机临床试验,共纳入 285884 名参与者。病例对照研究的荟萃分析显示,BP 与先前使用醛固酮拮抗剂(汇总 OR,1.75;95%CI,1.28-2.40)、二肽基肽酶 4 抑制剂(汇总 OR,1.92;95%CI,1.55-2.38)、抗胆碱能药物(汇总 OR,3.12;95%CI,1.54-6.33)和多巴胺能药物(汇总 OR,2.03;95%CI,1.34-3.05)之间存在显著关联。一项队列研究发现,接受二肽基肽酶 4 抑制剂治疗的患者发生 BP 的风险增加(风险比,2.38;95%CI,1.16-4.88;P=0.02)。一项试验发现,接受利拉利汀治疗的糖尿病患者发生 BP 的发生率更高(糖尿病组为 0.2%,安慰剂组为 0%)。
本系统评价和荟萃分析的结果表明,醛固酮拮抗剂、二肽基肽酶 4 抑制剂、抗胆碱能药物和多巴胺能药物与 BP 相关。这些药物应谨慎处方,特别是在患有老年和致残性神经疾病的高危患者中。