Tsai Ching-Piao, Lin Feng-Cheng, Lee Johnny Kuang-Wu, Lee Charles Tzu-Chi
Neurology, Neurological Institute, Taipei Veterans General Hospital and National Yang-Ming University.
J Epidemiol. 2015;25(2):172-7. doi: 10.2188/jea.JE20140070. Epub 2014 Dec 27.
The association of aspirin use and nonsteroid anti-inflammatory drug (NSAID) use with amyotrophic lateral sclerosis (ALS) risk is unclear. This study determined whether use of any individual compound is associated with ALS risk by conducting a total population-based case-control study in Taiwan.
A total of 729 patients with newly diagnosed ALS who had a severely disabling disease certificate between January 1, 2002, and December 1, 2008, comprised the case group. These cases were compared with 7290 sex-, age-, residence-, and insurance premium-matched controls. Drug use by each Anatomical Therapeutic Chemical code was analyzed using conditional logistic regression models. False discovery rate (FDR)-adjusted P values were reported in order to avoid inflating false positives.
Of the 1336 compounds, only the 266 with use cases exceeding 30 in our database were included in the screening analysis. Without controlling for steroid use, the analysis failed to reveal any compound that was inversely associated with ALS risk according to FDR criteria. After controlling for steroid use, we found use of the following compounds to be associated with ALS risk: aspirin, diphenhydramine (one of the antihistamines), and mefenamic acid (one of the NSAIDs). A multivariate analysis revealed that aspirin was independently inversely associated with ALS risk after controlling for diphenhydramine, mefenamic acid, and steroid use. The inverse association between aspirin and ALS was present predominately in patients older than 55 years.
The results of this study suggested that aspirin use might reduce the risk of ALS, and the benefit might be more prominent for older people.
阿司匹林和非甾体抗炎药(NSAID)的使用与肌萎缩侧索硬化症(ALS)风险之间的关联尚不清楚。本研究通过在台湾开展一项基于全人群的病例对照研究,确定使用任何单一化合物是否与ALS风险相关。
2002年1月1日至2008年12月1日期间,共有729例新诊断的患有严重致残疾病证明的ALS患者组成病例组。将这些病例与7290名性别、年龄、居住地和保险费匹配的对照进行比较。使用条件逻辑回归模型分析每个解剖治疗化学代码的药物使用情况。报告了错误发现率(FDR)调整后的P值,以避免假阳性增加。
在1336种化合物中,我们的数据库中仅筛选分析了使用病例超过30例的266种化合物。在不控制类固醇使用的情况下,根据FDR标准,分析未能发现任何与ALS风险呈负相关的化合物。在控制类固醇使用后,我们发现使用以下化合物与ALS风险相关:阿司匹林、苯海拉明(一种抗组胺药)和甲芬那酸(一种NSAID)。多变量分析显示,在控制苯海拉明、甲芬那酸和类固醇使用后,阿司匹林与ALS风险独立呈负相关。阿司匹林与ALS之间的负相关主要存在于55岁以上的患者中。
本研究结果表明,使用阿司匹林可能降低ALS风险,且对老年人的益处可能更为显著。