5PSQ-196 Association between phosphodiesterase 5 inhibitor use and incident dementia in prostate cancer patients treated with androgen deprivation therapy

Kc Chang, SC Shao, Jm Liu, E. Lai
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Abstract

Background and importance Recent studies have indicated that androgen deprivation therapy (ADT) increased the dementia risk in prostate cancer (PCa) patients. Phosphodiesterase 5 inhibitors (PDE5i) with nitric oxide mediated vasodilation can increase blood flow in the brain. However, no current studies have explored the association between PDE5i exposure and dementia in PCa patients treated with ADT. Aim and objectives To determine the association between PDE5i exposure and incident dementia in PCa patients treated with ADT. Material and methods We conducted a retrospective cohort study using the Chang Gung Research Database (CGRD) in Taiwan. We included PCa patients newly receiving ADT between 2009 and 2016. We conducted a three step matching and modified landmark approach to identify PDE5i users and non-users after ADT use. The landmark date was defined as 1 year following the start of ADT, and we defined PDE5i users as patients initiating PDE5i before and after the landmark date. We matched PDE5i users to non-users by (1) age, (2) prostatic specific antigen and (3) 1:4 propensity scores for comorbidity and co-medication. We followed the patients from the landmark date until the incident diagnosis of dementia, last date of clinical visit or 31 December 2019. We performed multivariate Cox proportional hazard models to compare the dementia risk between PDE5i users and non-users. Results We included 4557 PCa patients starting ADT treatment, with a mean age of 69.5 (SD 7.0) years. After matching, we identified 161 PDE5i users and 644 non-PDE5i users. A total of 5.1 person years of PDE5i users and 4.6 person years of PDE5i non-users were included. Compared with non-users of PDE5i, PCa patients treated with ADT initiating PDE5i had a lower risk of dementia (adjusted HR=0.17, 95% CI 0.04 to 0.70) in the modified landmark analyses. Conclusion and relevance PDE5i use in PCa patients treated with ADT was associated with a decreased risk of subsequent dementia. Future large scale studies are suggested to confirm our findings. References and/or acknowledgements Conflict of interest No conflict of interest
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5PSQ-196磷酸二酯酶5抑制剂的使用与雄激素剥夺治疗前列腺癌患者痴呆发生率的关系
背景和重要性近年来的研究表明,雄激素剥夺治疗(ADT)增加了前列腺癌(PCa)患者痴呆的风险。磷酸二酯酶5抑制剂(PDE5i)与一氧化氮介导的血管舒张可以增加脑血流量。然而,目前还没有研究探讨PDE5i暴露与ADT治疗的PCa患者痴呆之间的关系。目的和目的确定PDE5i暴露与ADT治疗的PCa患者发生痴呆之间的关系。材料与方法本研究利用台湾长庚研究数据库(CGRD)进行回顾性队列研究。我们纳入了2009年至2016年间新接受ADT治疗的PCa患者。我们进行了三步匹配和改进的里程碑方法来识别ADT使用后的PDE5i用户和非用户。里程碑日期定义为ADT开始后1年,我们将PDE5i使用者定义为在里程碑日期之前和之后开始使用PDE5i的患者。我们根据(1)年龄,(2)前列腺特异性抗原和(3)合并症和联合用药的1:4倾向评分将PDE5i使用者与非使用者进行匹配。我们从具有里程碑意义的日期开始跟踪患者,直到痴呆事件诊断,最后一次临床就诊日期或2019年12月31日。我们使用多变量Cox比例风险模型来比较PDE5i使用者和非使用者之间的痴呆风险。我们纳入了4557例开始ADT治疗的PCa患者,平均年龄为69.5岁(SD 7.0)。匹配后,我们确定了161个PDE5i用户和644个非PDE5i用户。PDE5i使用者共5.1人年,非PDE5i使用者共4.6人年。与未使用PDE5i的PCa患者相比,在修改的里程碑分析中,使用ADT启动PDE5i的PCa患者患痴呆的风险较低(调整HR=0.17, 95% CI 0.04至0.70)。PDE5i在接受ADT治疗的PCa患者中的使用与随后痴呆的风险降低相关。建议未来进行大规模研究以证实我们的发现。参考文献和/或致谢利益冲突无利益冲突
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