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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:二甲双胍使用和糖尿病男性中的所有原因和前列腺癌特异性死亡率。

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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)在糖尿病患者诊断和所有原因和PC特异性死亡率后累积二甲双胍使用的关联。我们使用了基于人口的追溯队列设计。数据是从几个安大略省医疗保健行政数据库获得的。在66岁的男性队列中,随后发育了PC的入射糖尿病,我们检查了PC诊断后抗糖尿病药物暴露持续时间对全因和PC特异性死亡率的影响。通过使用时变的Cox比例危害模型来计算粗糙和调整的危险比(HRS)以估计效果。队列由3,837名患者组成。 PC诊断中位年龄为75岁(局部范围[IQR],72至79岁)。在4.64年(IQR,2.7至7.1岁)的中位随访期间,1,343名(35%)死亡,291名患者(7.6%)由于PC而死亡。 PC诊断后二甲双胍治疗累计持续时间与剂量依赖的时尚以显着降低的PC特异性和全导致死亡率的显着降低有关。对于二甲双胍的每种额外6个月,PC特异性死亡率的调整后的HR为0.76(95%CI,0.64至0.89)。与全因死亡率的关联也显着,但随着时间的推移,从前6个月的人力资源增加0.76,达到24至30个月之间的0.93。其他抗糖尿病药物的累积使用与结果之间没有任何关系。在PC诊断后,在PC诊断后的累积二甲双胍暴露的累积持续时间与糖尿病男性的所有原因和PC特异性死亡率降低有关。

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