Negative Association of Proton Pump Inhibitors With Subsequent Development of Breast Cancer: A Nationwide Population-Based Study

被引:21
|
作者
Chen, Chao-Hung [1 ,2 ,3 ]
Lee, Cha-Ze [4 ]
Lin, Yi-Chun [5 ]
Kao, Li-Ting [6 ,7 ]
Lin, Herng-Ching [8 ,9 ]
机构
[1] Mackay Mem Hosp, Dept Thorac Surg, Taipei, Taiwan
[2] Mackay Jr Coll Med Nursing & Management, Dept Cosmet Applicat & Management, Taipei, Taiwan
[3] Taipei Med Univ, Coll Med, Res Ctr Sleep Med, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp & Coll Med, Dept Internal Med, Taipei, Taiwan
[5] Taipei Med Univ, Coll Management, Biostat Ctr, Taipei, Taiwan
[6] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[7] Triserv Gen Hosp, Dept Pharm Practice, Taipei, Taiwan
[8] Taipei Med Univ, Sch Hlth Care Adm, 250 Wu Hsing St, Taipei 11031, Taiwan
[9] Taipei Med Univ Hosp, Sleep Res Ctr, Taipei, Taiwan
来源
JOURNAL OF CLINICAL PHARMACOLOGY | 2019年 / 59卷 / 03期
关键词
breast cancer; epidemiology; proton pump inhibitors; RISK;
D O I
10.1002/jcph.1329
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although current evidence suggests potential antitumor activity of proton pump inhibitors (PPIs), there is no population-based evidence of an association between PPI use and subsequent breast cancer risks. We used an observational case-control study to examine the association between prior PPI use and breast cancer occurrence. Additional analysis examined dose-response and age-stratified associations of PPIs with breast cancer. This study used data from the Taiwan National Health Insurance Research Dataset. A total of 64,234 women diagnosed with breast cancer between 2004 and in 2013 were selected as cases. Controls were 64,234 women without cancer who were selected by matching them with cases on the basis of sociodemographic characteristics and widely prevalent comorbidities. Each study subject's claims data were tracked back for 5 years to determine precancer prescriptions of PPIs. Logistic regression modeling was used for the analysis. A total of 11,871 (9.24%) women had used PPIs within the prior 5 years, 8.06% and 10.42% among cases and controls, respectively. Breast cancer patients were 25% less likely to have had prior PPI exposure after adjustment for comorbidities that predispose to PPI exposure (95%CI 0.72-0.78) in the risk of breast cancer occurrence. A dose-response effect was also detected, with the highest effect, 35% lower PPI odds (95%CI 0.61-0.70) among patients in the highest exposure category. Our findings may suggest that women at a higher-than-average risk of breast cancer may benefit from PPI prescriptions if they have medical conditions that could benefit from PPIs.
引用
收藏
页码:350 / 355
页数:6
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