Hagberg Katrina Wilcox, Sahasrabuddhe Vikrant V, McGlynn Katherine A, Jick Susan S
Boston Collaborative Drug Surveillance Program and Boston University School of Public Health, Lexington, Massachusetts.
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
Pharmacotherapy. 2016 Feb;36(2):187-95. doi: 10.1002/phar.1704. Epub 2016 Feb 5.
It has been suggested that use of the antihypertensive drugs angiotensin-converting enzyme (ACE) inhibitors and β-blockers may decrease the risk of primary liver cancer; thus, the objective of this study was to evaluate whether use of ACE inhibitors and/or β-blockers is associated with a lower risk of liver cancer.
Nested case-control study.
United Kingdom Clinical Practice Research Datalink.
We identified 490 cases with hypertension and a first-time (incident) diagnosis of primary liver cancer between 1988 and 2011. To account for an induction period, the index date was defined as the date of the first recorded liver cancer diagnosis minus 1 year. Controls were selected from patients with hypertension in the CPRD during the study period with a recorded diagnosis of hypertension who had no diagnosis of liver cancer and were free of any other cancer (except nonmelanoma skin cancer) before the index date; they were matched up to a 4:1 ratio to cases based on index date (same index date as that of their matched case), age (same year of birth), sex, general practice, and number of years of recorded history in the CPRD before the index date (1909 controls). Both cases and controls were required to have at least 2 years of recorded activity in the database before the index date.
Exposure was defined as receipt of two or more prescriptions for ACE inhibitors and/or β-blockers before the index date; the reference group was nonuse (0-1 prescription) of ACE or β-blocker prescriptions before the index date. We also examined the effect of duration of use and, separately, the effect of individual drugs within each medication class on risk of liver cancer, and conducted analyses restricted to patients without liver disease or diabetes mellitus. Conditional logistic regression analysis was used to calculate odds ratios (ORs) and 95% confidence intervals (CIs). No association was found between use of ACE inhibitors and/or β-blockers and the risk of liver cancer compared with nonuse (adjusted OR 1.14, 95% CI 0.85-1.55). No significant differences were noted in risk by duration of use or by individual drugs, or after restricting the analyses to patients without diabetes or liver disease.
Use of ACE inhibitors and/or β-blockers was not associated with reduced risk of primary liver cancer compared with nonuse of these drugs in persons with hypertension.
有人提出,使用抗高血压药物血管紧张素转换酶(ACE)抑制剂和β受体阻滞剂可能会降低原发性肝癌的风险;因此,本研究的目的是评估使用ACE抑制剂和/或β受体阻滞剂是否与较低的肝癌风险相关。
巢式病例对照研究。
英国临床实践研究数据链。
我们确定了1988年至2011年间490例患有高血压且首次(新发)诊断为原发性肝癌的患者。为了考虑诱导期,索引日期定义为首次记录的肝癌诊断日期减去1年。对照组从研究期间CPRD中患有高血压且有高血压记录诊断、在索引日期前未诊断出肝癌且无任何其他癌症(非黑色素瘤皮肤癌除外)的患者中选取;根据索引日期(与匹配病例的索引日期相同)、年龄(出生年份相同)、性别、全科医疗以及索引日期前在CPRD中的记录病史年限,以4:1的比例与病例进行匹配(1909名对照)。病例和对照在索引日期前均需在数据库中有至少2年的记录活动。
暴露定义为在索引日期前接受两种或更多ACE抑制剂和/或β受体阻滞剂的处方;参照组为在索引日期前未使用(0 - 1张处方)ACE或β受体阻滞剂处方。我们还研究了使用持续时间的影响,以及分别研究每个药物类别中每种药物对肝癌风险的影响,并对无肝病或糖尿病的患者进行了分析。采用条件逻辑回归分析计算比值比(OR)和95%置信区间(CI)。与未使用相比,未发现使用ACE抑制剂和/或β受体阻滞剂与肝癌风险之间存在关联(调整后OR为1.14,95%CI为0.85 - 1.55)。在使用持续时间、个别药物方面,或在将分析限制于无糖尿病或肝病的患者后,均未发现风险有显著差异。
与未使用这些药物的高血压患者相比,使用ACE抑制剂和/或β受体阻滞剂与原发性肝癌风险降低无关。