Rodríguez-Miguel Antonio, Fernández-Antón Encarnación, Barreira-Hernández Diana, García-Rodríguez Luis A, Gil Miguel, García-Lledó Alberto, De Abajo Francisco J
Clinical Pharmacology Unit, University Hospital "Príncipe de Asturias", 28805 Alcalá de Henares, Spain.
Pharmacology Unit, Department of Biomedical Sciences, School of Medicine and Health Sciences, University of Alcalá (IRYCIS), 28805 Alcalá de Henares, Spain.
J Clin Med. 2022 Mar 10;11(6):1528. doi: 10.3390/jcm11061528.
(1) Background: The pleiotropic effects of statins may explain a chemoprotective action against colorectal cancer (CRC). Many studies have tested this hypothesis, but results have been inconsistent so far. Moreover, few have examined statins individually which is important for determining whether there is a class effect and if lipophilicity and intensity may play a role. (2) Methods: From 2001-2014, we carried out a study comprised of 15,491 incident CRC cases and 60,000 matched controls extracted from the primary healthcare database BIFAP. We fit a logistic regression model to compute the adjusted-odds ratios (AOR) with their 95% confidence intervals (CIs). Additionally, we carried out a systematic review and meta-analysis. (3) Results: Current use of statins showed a reduced risk of CRC (AOR = 0.87; 95% CI: 0.83-0.91) not sustained after discontinuation. The association was time-dependent, starting early (AOR = 0.85; 95% CI: 0.76-0.96) but weakened beyond 3-years. A class effect was suggested, although only significant for simvastatin and rosuvastatin. The risk reduction was more marked among individuals aged 70 or younger, and among moderate-high intensity users. Forty-eight studies were included in the meta-analysis (pooled-effect-size = 0.90; 95% CI: 0.86-0.93). (4) Conclusions: Results from the case-control study and the pooled evidence support a moderate chemoprotective effect of statins on CRC risk, modified by duration, intensity, and age.
(1) 背景:他汀类药物的多效性可能解释其对结直肠癌(CRC)的化学保护作用。许多研究已对这一假设进行了检验,但迄今为止结果并不一致。此外,很少有研究单独考察他汀类药物,而这对于确定是否存在类效应以及亲脂性和强度是否可能起作用很重要。(2) 方法:2001年至2014年,我们开展了一项研究,该研究包括从初级医疗保健数据库BIFAP中提取的15491例新发CRC病例和60000例匹配对照。我们拟合了一个逻辑回归模型来计算调整后的比值比(AOR)及其95%置信区间(CI)。此外,我们还进行了一项系统评价和荟萃分析。(3) 结果:当前使用他汀类药物显示CRC风险降低(AOR = 0.87;95%CI:0.83 - 0.91),停药后这种风险降低不再持续。这种关联具有时间依赖性,早期开始(AOR = 0.85;95%CI:0.76 - 0.96),但超过3年后减弱。提示存在类效应,尽管仅辛伐他汀和瑞舒伐他汀的效应显著。在70岁及以下个体以及中高强度使用者中,风险降低更为明显。荟萃分析纳入了48项研究(合并效应量 = 0.90;95%CI:0.86 - 0.93)。(4) 结论:病例对照研究结果和汇总证据支持他汀类药物对CRC风险具有适度的化学保护作用,这种作用受用药持续时间、强度和年龄的影响。