Clinical and Practice Research Group, School of Pharmacy, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, Northern Ireland, UK.
Cancer Causes Control. 2010 Dec;21(12):2093-100. doi: 10.1007/s10552-010-9628-0. Epub 2010 Aug 10.
To investigate the relationship between statin use and pancreatic cancer risk.
A nested case-control study was conducted within the UK GPRD. Cases had a diagnosis of primary malignant neoplasia of the exocrine pancreas. Controls were matched with cases on general practice site, sex and year of birth. Exposure of interest was exposure to statins since entry into the GPRD until 1 year before the case diagnosis date. Conditional logistic regression analyses were used to generate ORs and 95% CI associated with statin use compared to non-use.
A total of 1,141 pancreatic cancer cases and 7,954 controls were identified. Any use of a statin since entry into the GPRD (excluding the year prior to diagnosis) was not associated with the risk of pancreatic cancer OR 0.93 (95% CI, 0.76-1.14). Neither dose nor duration of statin use affected pancreatic cancer risk. When dose and duration of statin use combined were assessed, no evidence of reduced risk was seen for long-term users of high-dose statins OR 0.71 (0.42-1.20). Statin type (simvastatin vs atorvastatin) was not associated with pancreatic cancer risk.
Statin use at doses for managing hypercholesterolaemia, in a UK population, was not associated with the risk of exocrine pancreatic cancer.
研究他汀类药物使用与胰腺癌风险之间的关系。
在英国 GPRD 中进行了一项巢式病例对照研究。病例组有原发性胰腺外分泌恶性肿瘤的诊断。对照组与病例组在全科医生诊所、性别和出生年份上相匹配。研究的暴露因素是从进入 GPRD 到病例诊断日期前一年的他汀类药物暴露。采用条件逻辑回归分析生成与他汀类药物使用相关的比值比(OR)和 95%置信区间(CI),与未使用他汀类药物相比。
共确定了 1141 例胰腺癌病例和 7954 例对照。从进入 GPRD 开始(不包括诊断前一年)使用任何他汀类药物与胰腺癌风险无关,OR 为 0.93(95%CI,0.76-1.14)。他汀类药物的剂量和使用时间均不影响胰腺癌的风险。当评估他汀类药物的剂量和使用时间的综合影响时,未发现长期使用高剂量他汀类药物的患者风险降低,OR 为 0.71(0.42-1.20)。他汀类药物的类型(辛伐他汀与阿托伐他汀)与胰腺癌风险无关。
在英国人群中,使用剂量用于治疗高胆固醇血症的他汀类药物与外分泌性胰腺癌的风险无关。