Niikura Ryota, Hirata Yoshihiro, Hayakawa Yoku, Kawahara Takuya, Yamada Atsuo, Koike Kazuhiko
Department of Gastroenterology, Graduate School of Medicine The University of Tokyo Bunkyo-ku Japan.
Division of Advanced Genome Medicine The Institute of Medical Science, The University of Tokyo Bunkyo-ku Japan.
JGH Open. 2019 Jul 19;4(2):117-125. doi: 10.1002/jgh3.12226. eCollection 2020 Apr.
A number of recent studies have been published evaluating the chemopreventive effect of aspirin against gastric cancer, and an updated meta-analysis is required to evaluate this relationship further. This study presents a meta-analysis of studies examining the effect of aspirin on gastric cancer incidence and death.
The PUBMED and Cochrane Central Registration of Controlled Trials databases were searched for eligible studies published up to December 2018. Pooled risk ratios for gastric cancer incidence and death in aspirin users nonusers were determined using fixed- and random-effects models. The influence of the frequency of aspirin use, duration of aspirin use, and geographic location on gastric cancer incidence was evaluated.
The meta-analysis comprised 33 studies with a total of 1 927 971 patients. The pooled risk ratios for gastric cancer incidence in the fixed- and random-effects models were 0.890 (95% confidence interval, 0.871-0.909) and 0.826 (0.740-0.922), respectively. In Asia and North America, the maximum preventive benefit of aspirin use was observed with weekly or daily use. Aspirin use was most effective for noncardiac gastric cancer. The pooled risk ratios for gastric cancer death in the fixed- and random-effects models were 0.798 (0.749-0.850) and 0.894 (0.780-1.024), respectively. Significant heterogeneity was observed among studies of gastric cancer incidence but not gastric cancer death.
Aspirin use may reduce the risk of gastric cancer incidence and death; however, the relationship may be limited to a specific frequency and duration of aspirin use and geographic location.
近期已发表了多项评估阿司匹林对胃癌化学预防作用的研究,需要进行一项更新的荟萃分析来进一步评估这种关系。本研究对考察阿司匹林对胃癌发病率和死亡率影响的研究进行了荟萃分析。
检索了PUBMED和Cochrane对照试验中心注册库,查找截至2018年12月发表的符合条件的研究。使用固定效应模型和随机效应模型确定阿司匹林使用者与非使用者中胃癌发病率和死亡率的合并风险比。评估了阿司匹林使用频率、使用持续时间和地理位置对胃癌发病率的影响。
该荟萃分析纳入了33项研究,共1927971例患者。固定效应模型和随机效应模型中胃癌发病率的合并风险比分别为0.890(95%置信区间,0.871 - 0.909)和0.826(0.740 - 0.922)。在亚洲和北美,每周或每日使用阿司匹林可观察到最大的预防益处。阿司匹林对非心源性胃癌最为有效。固定效应模型和随机效应模型中胃癌死亡的合并风险比分别为0.798(0.749 - 0.850)和0.894(0.780 - 1.024)。在胃癌发病率的研究中观察到显著的异质性,但在胃癌死亡的研究中未观察到。
使用阿司匹林可能降低胃癌发病率和死亡率;然而,这种关系可能仅限于阿司匹林使用的特定频率、持续时间和地理位置。