Institution of Occupational Medicine and Industrial Hygiene, National Taiwan University College of Public Health bDepartment of Internal Medicine, Taipei City Hospital, Zhongxing Branch, Taipei, Taiwan.
J Hypertens. 2012 Dec;30(12):2432-9. doi: 10.1097/HJH.0b013e328358d42f.
Angiotensin-converting enzyme (ACE) inhibitors are first-line antihypertensive and potential cancer preventive agents. Interest in breast cancer prevention is growing, and more clinical evidence is needed regarding the effects of preventive therapy, alone or in combination.
This was a nationwide case-control analysis from the Taiwan National health Insurance Research Database. We analyzed 16,847 female breast cancer patients (diagnosed between 1 January 2002 and 31 December 2008) and 50,541 matched individuals. Longitudinal exposure to ACE inhibitors and cyclooxygenase inhibitors was compared.
The risk of developing breast cancer among patients taking both aspirin and an ACE inhibitor decreased as the ACE inhibitor dose increased. Among patients receiving between 28 and 364 cumulative defined daily doses (cDDDs) of aspirin, the adjusted odds ratios (ORs) were 0.97 (0.90-1.06), 0.91 (0.82-1.03), and 0.79 (0.68-0.92) for women taking ACE inhibitors for 0-27, 28-364, and more than 365 cDDD, respectively. Among women receiving more than 365 cDDD of aspirin, the adjusted ORs were 0.91 (0.80-1.03), 0.81 (0.70-0.94), and 0.81 (0.71-0.92) as the ACE inhibitor dose increased, respectively. Women taking nonaspirin NSAIDs along with an ACE inhibitor had the same finding. Among women taking 28-364 cDDD of NSAIDs, the adjusted ORs were 0.85 (0.81-0.89), 0.87 (0.81-0.94), and 0.80 (0.73-0.88); for women receiving more than 365 cDDD of NSAIDs, the adjusted ORs were 0.68 (0.62-0.74), 0.61 (0.53-0.70), and 0.60 (0.52-0.70) as the ACE inhibitor dose increased, respectively.
The findings of this nationwide analysis support the hypothesis that ACE inhibitors enhance the antitumor effect of cyclooxygenase inhibitors on breast cancer.
血管紧张素转换酶(ACE)抑制剂是一线降压药和潜在的癌症预防药物。人们对乳腺癌预防的兴趣日益浓厚,需要更多关于预防治疗的临床证据,包括单独使用或联合使用时的效果。
这是一项来自台湾全民健康保险研究数据库的全国性病例对照分析。我们分析了 16847 名女性乳腺癌患者(2002 年 1 月 1 日至 2008 年 12 月 31 日诊断)和 50541 名匹配个体。比较了长期服用 ACE 抑制剂和环氧化酶抑制剂的情况。
在服用阿司匹林和 ACE 抑制剂的患者中,随着 ACE 抑制剂剂量的增加,发生乳腺癌的风险降低。在接受 28 至 364 个累积定义日剂量(cDDD)阿司匹林的患者中,女性服用 ACE 抑制剂的调整后比值比(OR)分别为 0.97(0.90-1.06)、0.91(0.82-1.03)和 0.79(0.68-0.92),剂量分别为 0-27、28-364 和大于 365 cDDD。在服用超过 365 cDDD 阿司匹林的女性中,随着 ACE 抑制剂剂量的增加,调整后的 OR 分别为 0.91(0.80-1.03)、0.81(0.70-0.94)和 0.81(0.71-0.92)。同时服用非阿司匹林非甾体抗炎药(NSAIDs)和 ACE 抑制剂的女性也有同样的发现。在服用 28-364 cDDD 非甾体抗炎药的女性中,调整后的 OR 分别为 0.85(0.81-0.89)、0.87(0.81-0.94)和 0.80(0.73-0.88);在服用超过 365 cDDD 非甾体抗炎药的女性中,调整后的 OR 分别为 0.68(0.62-0.74)、0.61(0.53-0.70)和 0.60(0.52-0.70)。
这项全国性分析的结果支持 ACE 抑制剂增强环氧化酶抑制剂对乳腺癌抗肿瘤作用的假说。