From the Department of Medicine, The University of Hong Kong, Queen Mary Hospital (K.S.C., W.K.S., W.K.L.).
Department of Pharmacology and Pharmacy, Centre for Safe Medication Practice and Research, The University of Hong Kong (E.W.C., I.C.K.W.).
Hypertension. 2020 Sep;76(3):968-975. doi: 10.1161/HYPERTENSIONAHA.120.15317. Epub 2020 Jul 6.
Whether ACE (angiotensin-converting enzyme) inhibitors and angiotensin receptor blockers modify colorectal cancer risk remains controversial. We aimed to determine association between their use and colorectal cancer risk after a negative baseline colonoscopy. This is a territory-wide retrospective cohort study recruiting patients aged ≥40 who had undergone colonoscopy between 2005 and 2013. Exclusion criteria included colorectal cancer detected <6 months of index colonoscopy, prior colorectal cancer, inflammatory bowel disease, and prior colectomy. The primary outcome was colorectal cancer diagnosed between 6 and 36 months after index colonoscopy. Sites of colorectal cancer were categorized as proximal (proximal to splenic flexure) and distal cancer. The adjusted hazard ratio of colorectal cancer with ACE inhibitor/angiotensin receptor blocker use (≥180-day use within 5 years before index colonoscopy) was derived by propensity score regression adjustment of 23 covariates (including patient's factors, concurrent medication use, and endoscopy center's performance). Of 187 897 eligible patients, 30 856 (16.4%) were ACE inhibitors/angiotensin receptor blocker users. Eight hundred fifty-four (0.45%) developed colorectal cancer between 6 and 36 months after index colonoscopy (proximal cancer: 147 [17.2%]). These drugs were associated with lower risk of colorectal cancer that developed <3 years after index colonoscopy (adjusted hazard ratio, 0.78 [95% CI, 0.64-0.96]), but not colorectal cancer that developed >3years (adjusted hazard ratio, 1.18 [95% CI, 0.88-1.57]); every single year increase in the drug use was associated with 5% reduction in adjusted hazard ratio risk. ACE inhibitors/angiotensin receptor blocker were associated with a lower colorectal cancer risk in a duration-response manner.
无论血管紧张素转换酶(ACE)抑制剂和血管紧张素受体阻滞剂是否会改变结直肠癌的风险仍存在争议。我们的目的是在基线结肠镜检查结果为阴性后,确定这些药物的使用与结直肠癌风险之间的关系。这是一项全港范围的回顾性队列研究,纳入了 2005 年至 2013 年间接受过结肠镜检查且年龄≥40 岁的患者。排除标准包括在索引结肠镜检查后<6 个月发现结直肠癌、既往结直肠癌、炎症性肠病和既往结肠切除术。主要结局是在索引结肠镜检查后 6 至 36 个月间诊断为结直肠癌。结直肠癌的部位分为近端(脾曲前)和远端癌。通过倾向评分回归调整 23 个协变量(包括患者因素、同时使用的药物和内镜中心的表现),得出 ACE 抑制剂/血管紧张素受体阻滞剂使用者(在索引结肠镜检查前 5 年内使用≥180 天)的结直肠癌调整后的危险比。在 187897 名合格患者中,有 30856 名(16.4%)是 ACE 抑制剂/血管紧张素受体阻滞剂使用者。854 名(0.45%)患者在索引结肠镜检查后 6 至 36 个月间发生结直肠癌(近端癌:147 例[17.2%])。这些药物与索引结肠镜检查后<3 年发生的结直肠癌风险降低相关(调整后的危险比,0.78[95%CI,0.64-0.96]),但与索引结肠镜检查后>3 年发生的结直肠癌风险无关(调整后的危险比,1.18[95%CI,0.88-1.57]);药物使用年限每增加一年,调整后的危险比风险降低 5%。ACE 抑制剂/血管紧张素受体阻滞剂与结直肠癌风险呈剂量反应关系。