From the Division of Cardiology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Allergy Asthma Proc. 2023 Sep 1;44(5):345-353. doi: 10.2500/aap.2023.44.230035.
Proton-pump inhibitors (PPI) are among the most widely used drugs worldwide. However, the association between PPI use and the risk of asthma remains unclear. To investigate the association between PPI use and subsequent asthma risk. We included participants from the Taiwan National Health Insurance Research Database between 1999 and 2013. Patients who used PPIs and experienced new-onset asthma (n = 20,344) were assigned to the case cohort and matched in a 1:1 ratio with controls who did not subsequently develop asthma. PPI use was defined as > 30 cumulative defined daily doses (cDDD); non-PPI use was defined as ≤ 30 cDDDs. The Charlson Comorbidity Index (CCI) score was used for clinical prognosis and comorbidity adjustment. Multivariate Cox regression models were used for the calculation of adjusted odds ratios (OR). There was a significant and dose-dependent association between PPI use and the risk of developing asthma. The adjusted ORs were 1.24 (95% confidence interval [CI], 1.15-1.33), 1.39 (95% CI, 1.28-1.50), and 1.61 (95% CI, 1.43-1.81) for the male subject with 31-120 cDDDs, 120-365 cDDDs, and >365 cDDDs, respectively, compared with PPI nonusers. Men were at higher risk of developing asthma with longer PPI use compared with women. Stratified analyses based on the PPI type showed that exposure to lansoprazole, pantoprazole, omeprazole, and esomeprazole was associated with subsequent asthma risk. Extended use of PPIs was found to be linked to an increased risk of asthma development. This association remained consistent across different age groups, sexes, demographic factors, indications for PPI use, CCI scores, and other atopic diseases. However, further prospective studies are required to elucidate the causal mechanisms involved.
质子泵抑制剂(PPI)是全球应用最广泛的药物之一。然而,PPI 使用与哮喘风险之间的关系尚不清楚。为了研究 PPI 使用与随后发生哮喘风险之间的关系。我们纳入了 1999 年至 2013 年期间来自台湾全民健康保险研究数据库的参与者。使用 PPI 并出现新发哮喘(n = 20,344)的患者被分配到病例队列,并与未随后发生哮喘的对照组按 1:1 比例匹配。PPI 使用定义为 > 30 累积定义日剂量(cDDD);非 PPI 使用定义为 ≤ 30 cDDD。Charlson 合并症指数(CCI)评分用于临床预后和合并症调整。多变量 Cox 回归模型用于计算调整后的优势比(OR)。PPI 使用与发生哮喘的风险之间存在显著且剂量依赖性的关联。调整后的 OR 分别为 1.24(95%置信区间 [CI],1.15-1.33)、1.39(95% CI,1.28-1.50)和 1.61(95% CI,1.43-1.81),用于男性受试者,分别为 31-120 cDDD、120-365 cDDD 和 >365 cDDD,与非 PPI 使用者相比。与女性相比,男性使用 PPI 的时间越长,患哮喘的风险越高。基于 PPI 类型的分层分析表明,暴露于兰索拉唑、泮托拉唑、奥美拉唑和埃索美拉唑与随后发生哮喘的风险相关。长期使用 PPI 与哮喘发病风险增加相关。这种关联在不同年龄组、性别、人口统计学因素、PPI 使用指征、CCI 评分和其他特应性疾病中均保持一致。然而,需要进一步的前瞻性研究来阐明所涉及的因果机制。