Sleiman Joelle, Kreidieh Malek, Lee Un Jung, Khouri Peter, Plann-Curley Brendan, Sison Cristina, Deeb Liliane
Department of Internal Medicine, Staten Island University Hospital, Northwell Health, Staten Island, NY, USA.
Division of Gastroenterology, Department of Internal Medicine, Staten Island University Hospital, Northwell Health, Staten Island, NY, USA.
Gastroenterology Res. 2025 Jun;18(3):108-118. doi: 10.14740/gr2028. Epub 2025 Jun 4.
Statins are reported to reduce colorectal cancer (CRC) risk in the general population, but their effect on individuals with inflammatory bowel disease (IBD) remains uncertain. We aimed to evaluate the relationship between statin use and CRC risk in patients with IBD.
A comprehensive review of the literature was conducted on PubMed, Web of Science, and EMBASE to evaluate the association between statin use and the development of CRC in patients with IBD. After deduplication, there were 324 studies screened, and those reporting odds ratios (ORs) or hazard ratios (HRs) for CRC risk in IBD patients using statins were included. The primary endpoints included the development of CRC (OR) and time to CRC (HR). A meta-analysis utilizing fixed or random-effects models, heterogeneity tests, and a funnel plot was performed in R (version 4.3.0) with alpha of 0.05.
This meta-analysis included seven studies involving 59,596 patients: three for OR (11,116 patients) and four for HR (48,480 patients). The pooled OR was 0.22 (95% confidence interval (CI): 0.01 - 7.81), suggesting 78% lower odds of CRC in statin users, though not statistically significant (P = 0.21), with potential publication bias. The pooled HR was 0.77 (95% CI: 0.63 - 0.94), indicating a significant 23% reduction in CRC hazard for statin users (P < 0.05), with low publication bias.
Our meta-analysis showed that statin use is associated with a reduced risk of CRC in IBD, significant in HR-based but not in OR-based analysis. Large randomized controlled trials are needed to clarify the duration of statin use and their chemopreventive effects, independent of factors such as targeted therapy for chronic mucosal inflammation.
据报道,他汀类药物可降低普通人群患结直肠癌(CRC)的风险,但其对炎症性肠病(IBD)患者的影响仍不确定。我们旨在评估IBD患者使用他汀类药物与CRC风险之间的关系。
对PubMed、Web of Science和EMBASE进行全面的文献综述,以评估IBD患者使用他汀类药物与CRC发生之间的关联。在去除重复项后,筛选出324项研究,纳入那些报告使用他汀类药物的IBD患者患CRC风险的比值比(OR)或风险比(HR)的研究。主要终点包括CRC的发生(OR)和CRC发生时间(HR)。在R(版本4.3.0)中使用固定或随机效应模型、异质性检验和漏斗图进行荟萃分析,α值为0.05。
该荟萃分析纳入了7项研究,涉及59,596名患者:3项研究用于OR分析(11,116名患者),4项研究用于HR分析(48,480名患者)。汇总OR为0.22(95%置信区间(CI):0.01 - 7.81),表明他汀类药物使用者患CRC的几率降低78%,尽管无统计学意义(P = 0.21),存在潜在的发表偏倚。汇总HR为0.77(95%CI:0.63 - 0.94),表明他汀类药物使用者患CRC的风险显著降低23%(P < 0.05),发表偏倚较低。
我们的荟萃分析表明,IBD患者使用他汀类药物与CRC风险降低相关,基于HR的分析具有显著性,但基于OR的分析无显著性。需要大型随机对照试验来明确他汀类药物的使用时长及其化学预防效果,独立于慢性黏膜炎症靶向治疗等因素。