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首页> 外文期刊>Journal of Clinical Oncology >Metformin Use and All-Cause and Prostate Cancer-Specific Mortality Among Men With Diabetes.
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Metformin Use and All-Cause and Prostate Cancer-Specific Mortality Among Men With Diabetes.

机译:二甲双胍的使用以及糖尿病男性的全因和前列腺癌死亡率。

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摘要

To evaluate the association between cumulative duration of metformin use after prostate cancer (PC) diagnosis and all-cause and PC-specific mortality among patients with diabetes.We used a population-based retrospective cohort design. Data were obtained from several Ontario health care administrative databases. Within a cohort of men older than age 66 years with incident diabetes who subsequently developed PC, we examined the effect of duration of antidiabetic medication exposure after PC diagnosis on all-cause and PC-specific mortality. Crude and adjusted hazard ratios (HRs) were calculated by using a time-varying Cox proportional hazard model to estimate effects.The cohort consisted of 3,837 patients. Median age at diagnosis of PC was 75 years (interquartile range [IQR], 72 to 79 years). During a median follow-up of 4.64 years (IQR, 2.7 to 7.1 years), 1,343 (35%) died, and 291 patients (7.6%) died as a result of PC. Cumulative duration of metformin treatment after PC diagnosis was associated with a significant decreased risk of PC-specific and all-cause mortality in a dose-dependent fashion. Adjusted HR for PC-specific mortality was 0.76 (95% CI, 0.64 to 0.89) for each additional 6 months of metformin use. The association with all-cause mortality was also significant but declined over time from an HR of 0.76 in the first 6 months to 0.93 between 24 and 30 months. There was no relationship between cumulative use of other antidiabetic drugs and either outcome.Increased cumulative duration of metformin exposure after PC diagnosis was associated with decreases in both all-cause and PC-specific mortality among diabetic men.
机译:为了评估前列腺癌(PC)诊断后二甲双胍的累积使用时间与糖尿病患者全因和PC特异性死亡率之间的关系,我们使用了基于人群的回顾性队列设计。数据是从几个安大略省医疗保健管理数据库中获得的。在随后发生PC的66岁以上患有糖尿病的男性队列中,我们检查了PC诊断后服用抗糖尿病药物持续时间对全因和PC特异性死亡率的影响。通过使用随时间变化的Cox比例风险模型估算效果来计算粗略和调整的风险比(HRs)。该队列包括3,837名患者。诊断为PC的中位年龄为75岁(四分位间距[IQR]为72至79岁)。在平均随访时间为4.64年(IQR,2.7至7.1年)中,因PC死亡1,343人(35%),有291例患者(7.6%)死亡。 PC诊断后二甲双胍治疗的累积持续时间与PC特异性和全因死亡率的降低的风险显着相关(呈剂量依赖性)。使用二甲双胍每增加6个月,针对PC特异性死亡率的调整后HR为0.76(95%CI,0.64至0.89)。与全因死亡率的关联也很显着,但随着时间的流逝从最初6个月的0.76 HR下降到24到30个月的0.93。其他抗糖尿病药物的累积使用与任何一种结局之间都没有关系。PC诊断后二甲双胍暴露累积持续时间的增加与糖尿病男性全因死亡率和PC特异性死亡率的降低有关。

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