Tsai Min-Lan, Lin Hsiu-Chen, Yen Chiung-Hui, Ku Jung-Tzu, Sung Shian-Ying, Chang Hsi
Department of Pediatrics, Taipei Medical University Hospital, Taipei 110, Taiwan.
Department of Pediatrics, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Children (Basel). 2022 Oct 22;9(11):1607. doi: 10.3390/children9111607.
(1) Background: Cysteinyl leukotriene receptor antagonists (LTRAs), including montelukast and zafirlukast, are FDA-approved for treating pediatric asthma and allergic diseases. Tourette syndrome (TS), a common neuropsychiatric disorder in children, is associated with allergic diseases and asthma. In this study, we investigated the risk of TS following an LTRA prescription for pediatric allergic diseases. (2) Methods: Children younger than 18 years of age who were newly diagnosed with asthma, allergic rhinitis, or atopic dermatitis between 1 January 2005 and 31 December 2018 and who were registered in the Taiwan National Health Insurance Research Database, which comprises the medical records of nearly 23 million Taiwanese population, were enrolled. LTRA users were matched with randomly selected LTRA non-users by sex, age, asthma-diagnosis year, and urbanization level. In total, 26,984 participants with allergic disease and TS were enrolled and included in the Cox proportional hazards model analysis. (3) Results: Children with allergic disease and asthma treated with LTRAs had a higher risk for TS than LTRA non-users (adjusted hazard ratio 1.376 [95% CI: 1.232−1.536], p < 0.001). LTRA users had a significantly higher risk for TS than LTRA non-users with allergic disease. The cumulative incidence of TS was significantly higher in LTRA users than in non-users with allergic diseases and asthma (log-rank test, p < 0.0001). (4) Conclusion: A prescription of LTRAs, mainly montelukast, increased the risk of TS among children with asthma, allergic rhinitis, or atopic dermatitis. The mechanism underlying the neuropsychiatric effect of LTRAs needs further investigation.
(1)背景:半胱氨酰白三烯受体拮抗剂(LTRA),包括孟鲁司特和扎鲁司特,已获美国食品药品监督管理局(FDA)批准用于治疗儿童哮喘和过敏性疾病。抽动秽语综合征(TS)是儿童常见的神经精神疾病,与过敏性疾病和哮喘有关。在本研究中,我们调查了儿童过敏性疾病使用LTRA处方后发生TS的风险。(2)方法:纳入2005年1月1日至2018年12月31日期间新诊断为哮喘、过敏性鼻炎或特应性皮炎且年龄小于18岁并登记在台湾国民健康保险研究数据库中的儿童,该数据库包含近2300万台湾人口的医疗记录。LTRA使用者按性别、年龄、哮喘诊断年份和城市化水平与随机选择的非LTRA使用者进行匹配。总共纳入26984名患有过敏性疾病和TS的参与者并纳入Cox比例风险模型分析。(3)结果:接受LTRA治疗的过敏性疾病和哮喘儿童发生TS的风险高于非LTRA使用者(调整后风险比1.376 [95%可信区间:1.232 - 1.536],p < 0.001)。LTRA使用者发生TS的风险显著高于患有过敏性疾病的非LTRA使用者。LTRA使用者中TS的累积发病率显著高于患有过敏性疾病和哮喘的非使用者(对数秩检验,p < 0.0001)。(4)结论:LTRA处方,主要是孟鲁司特,增加了哮喘、过敏性鼻炎或特应性皮炎儿童发生TS的风险。LTRA神经精神效应的潜在机制需要进一步研究。