Department of Medicine, Section of Epidemiology and Population Sciences, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Departments of Neurology and Preventive Medicine, University of Southern California, Keck School of Medicine, Los Angeles, California.
Cancer Epidemiol Biomarkers Prev. 2019 Mar;28(3):555-562. doi: 10.1158/1055-9965.EPI-18-0702. Epub 2018 Nov 27.
There have been few studies of sufficient size to address the relationship between glioma risk and the use of aspirin or NSAIDs, and results have been conflicting. The purpose of this study was to examine the associations between glioma and aspirin/NSAID use, and to aggregate these findings with prior published studies using meta-analysis.
The Glioma International Case-Control Study (GICC) consists of 4,533 glioma cases and 4,171 controls recruited from 2010 to 2013. Interviews were conducted using a standardized questionnaire to obtain information on aspirin/NSAID use. We examined history of regular use for ≥6 months and duration-response. Restricted maximum likelihood meta-regression models were used to aggregate site-specific estimates, and to combine GICC estimates with previously published studies.
A history of daily aspirin use for ≥6 months was associated with a 38% lower glioma risk, compared with not having a history of daily use [adjusted meta-OR = 0.62; 95% confidence interval (CI), 0.54-0.70]. There was a significant duration-response trend ( = 1.67 × 10), with lower ORs for increasing duration of aspirin use. Duration-response trends were not observed for NSAID use. In the meta-analysis aggregating GICC data with five previous studies, there was a marginally significant association between use of aspirin and glioma (mOR = 0.84; 95% CI, 0.70-1.02), but no association for NSAID use.
Our study suggests that aspirin may be associated with a reduced risk of glioma.
These results imply that aspirin use may be associated with decreased glioma risk. Further research examining the association between aspirin use and glioma risk is warranted.
已有少数研究的规模足以解决胶质瘤风险与阿司匹林或 NSAIDs 使用之间的关系,但结果相互矛盾。本研究的目的是检查胶质瘤与阿司匹林/NSAID 使用之间的关联,并使用荟萃分析汇总以前发表的研究结果。
Glioma International Case-Control Study(GICC)由 2010 年至 2013 年间招募的 4533 例胶质瘤病例和 4171 例对照组成。访谈采用标准化问卷进行,以获取关于阿司匹林/NSAID 使用的信息。我们检查了≥6 个月的定期使用史和时间-反应。受限最大似然元回归模型用于汇总特定部位的估计值,并将 GICC 估计值与以前发表的研究相结合。
与没有每日使用史相比,每日使用阿司匹林≥6 个月与胶质瘤风险降低 38%相关[调整后的 meta-OR = 0.62;95%置信区间(CI),0.54-0.70]。存在显著的时间-反应趋势( = 1.67×10),随着阿司匹林使用时间的增加,比值比降低。未观察到 NSAID 使用的时间-反应趋势。在荟萃分析中将 GICC 数据与五项先前研究相结合时,阿司匹林使用与胶质瘤之间存在边缘显著的关联(mOR = 0.84;95%CI,0.70-1.02),但 NSAID 使用没有关联。
我们的研究表明,阿司匹林可能与降低胶质瘤风险有关。
这些结果表明,阿司匹林的使用可能与降低胶质瘤风险有关。需要进一步研究检查阿司匹林使用与胶质瘤风险之间的关联。