Division of Urology, Department of Surgery, Changhua Christian Hospital, Changhua, Taiwan.
School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Prostate Cancer Prostatic Dis. 2017 Sep;20(3):328-333. doi: 10.1038/pcan.2017.14. Epub 2017 Apr 11.
Clinical observations indicated an increased risk of developing prostate cancer in gout patients. Chronic inflammation is postulated to be one crucial mechanism for prostate carcinogenesis. Allopurinol, a widely used antigout agent, possesses potent anti-inflammation capacity. We elucidated whether allopurinol decreases the risk of prostate cancer in gout patients.
We analyzed data retrieved from Taiwan National Health Insurance Database between January 2000 and December 2012. Patients diagnosed with gout during the study period with no history of prostate cancer and who had never used allopurinol were selected. Four allopurinol use cohorts (that is, allopurinol use (>365 days), allopurinol use (181-365 days), allopurinol use (91-180 days) and allopurinol use (31-90 days)) and one cohort without using allopurinol (that is, allopurinol use (No)) were included. The study end point was the diagnosis of new-onset prostate cancer. Multivariable Cox proportional hazards regression and propensity score-adjusted Cox regression models were used to estimate the association between the risk of prostate cancer and allopurinol treatment in gout patients after adjusting for potential confounders.
A total of 25 770 gout patients (aged between 40 and 100 years) were included. Multivariable Cox regression analyses revealed that the risk of developing prostate cancer in the allopurinol use (>365 days) cohort was significantly lower than the allopurinol use (No) cohort (adjusted hazard ratio (HR)=0.64, 95% confidence interval (CI)=0.45-0.9, P=0.011). After propensity score adjustment, the trend remained the same (adjusted HR=0.66, 95% CI=0.46-0.93, P=0.019).
Long-term (more than 1 year) allopurinol use may associate with a decreased risk of prostate cancer in gout patients.
临床观察表明,痛风患者患前列腺癌的风险增加。慢性炎症被认为是前列腺癌发生的一个关键机制。别嘌醇是一种广泛使用的抗痛风药物,具有很强的抗炎能力。我们探讨了别嘌醇是否降低痛风患者患前列腺癌的风险。
我们分析了 2000 年 1 月至 2012 年 12 月期间从台湾国家健康保险数据库中检索到的数据。选择在研究期间诊断为痛风且无前列腺癌病史且从未使用过别嘌醇的患者。共纳入 4 个别嘌醇使用队列(即别嘌醇使用 (>365 天)、别嘌醇使用 (181-365 天)、别嘌醇使用 (91-180 天) 和别嘌醇使用 (31-90 天))和一个未使用别嘌醇的队列(即别嘌醇使用 (No))。研究终点是新诊断的前列腺癌。多变量 Cox 比例风险回归和倾向评分调整的 Cox 回归模型用于估计在调整潜在混杂因素后,痛风患者中前列腺癌风险与别嘌醇治疗之间的关系。
共纳入 25770 例痛风患者(年龄 40-100 岁)。多变量 Cox 回归分析显示,别嘌醇使用 (>365 天) 队列发生前列腺癌的风险明显低于别嘌醇使用 (No) 队列(调整后的危险比 (HR)=0.64,95%置信区间 (CI)=0.45-0.9,P=0.011)。在倾向评分调整后,趋势仍然相同(调整后的 HR=0.66,95% CI=0.46-0.93,P=0.019)。
长期(超过 1 年)使用别嘌醇可能与痛风患者前列腺癌风险降低相关。