Randazzo Marco, Beatrice Josef, Huber Andreas, Grobholz Rainer, Manka Lukas, Wyler Stephen F, Chun Felix F, Recker Franz, Kwiatkowski Maciej
Department of Urology, Cantonal Hospital Aarau, Aarau, 5001, Switzerland,
World J Urol. 2015 Aug;33(8):1189-96. doi: 10.1007/s00345-014-1426-y. Epub 2014 Oct 31.
To analyze the effect of the oral antidiabetic drug metformin on PSA level, free-to-total PSA ratio (f/t-ratio), PCa incidence and grade as well as mortality in men participating in a population-based screening trial.
Data from 4,314 men aged 55-70 years from a population-based PSA-screening trial (ERSPC Aarau) were analyzed. Information on metformin exposure was obtained by a self-administered questionnaire. Serum PSA threshold at ≥3 ng/ml triggered prostate biopsy. Data on PCa incidence and mortality were obtained through registry linkages.
Median follow-up time was 7.6 years. Mean age at baseline was 65.5 years (±SD 4.4). In all, n = 150 (3.5 %) men used metformin [metf+]. Mean baseline PSA levels were comparable between both groups ([metf+] 1.6 ng/ml ± 2.4 vs. [metf-] 1.8ug/l ± 2.2, p = 0.4) while f/t-ratio was slightly higher in metformin users ([metf+] 30.7 % ± 10.9 vs. [metf-] 27.3 % ± 10.9, p = 0.01). Overall, n = 372 (8.6 %) PCa cases were detected. Neither cumulative PCa incidence (n = 11; 7.3 % [metf+] vs. n = 361 8.7 % [metf-]; p = 0.5) nor d`Amico risk groups were significantly different between both groups. One man in each group (metf+ 0.7 % and metf- 0.02 %) died from PCa (p < 0.0001), respectively. All-cause mortality was significantly higher among met + compared to met- (adjusted OR 2.50, 95 %CI 1.59-3.82; p = 0.0001).
No significant differences in PSA levels or PCa incidence and grade were observed. The slightly higher f/t-ratio did not result in lower PCa detection rate. Metformin users were at significantly higher risk of all-cause mortality. The relatively small number of men on metformin is a main limitation of the study.
分析口服抗糖尿病药物二甲双胍对参与一项基于人群的筛查试验的男性的前列腺特异性抗原(PSA)水平、游离PSA与总PSA比值(f/t比值)、前列腺癌(PCa)发病率和分级以及死亡率的影响。
分析了来自一项基于人群的PSA筛查试验(阿劳欧洲随机前列腺癌筛查试验)中4314名年龄在55至70岁之间男性的数据。通过一份自我填写的问卷获取二甲双胍暴露信息。血清PSA阈值≥3 ng/ml时进行前列腺活检。通过登记链接获取PCa发病率和死亡率数据。
中位随访时间为7.6年。基线时的平均年龄为65.5岁(标准差±4.4)。共有n = 150名(3.5%)男性使用二甲双胍[二甲双胍使用者组]。两组的平均基线PSA水平相当([二甲双胍使用者组]1.6 ng/ml±2.4,[非二甲双胍使用者组]1.8 ng/ml±2.2,p = 0.4),而二甲双胍使用者的f/t比值略高([二甲双胍使用者组]30.7%±10.9,[非二甲双胍使用者组]27.3%±10.9,p = 0.01)。总体上,共检测到n = 372例(8.6%)PCa病例。两组之间的累积PCa发病率(n = 11;7.3%[二甲双胍使用者组]对n = 361;8.7%[非二甲双胍使用者组];p = 0.5)和达米科风险组均无显著差异。每组各有一名男性(二甲双胍使用者组0.7%和非二甲双胍使用者组0.02%)死于PCa(p < 0.0001)。与非二甲双胍使用者相比,二甲双胍使用者的全因死亡率显著更高(校正后的比值比2.50,95%置信区间1.59 - 3.82;p = 0.0001)。
未观察到PSA水平、PCa发病率和分级有显著差异。f/t比值略高并未导致PCa检测率降低。二甲双胍使用者的全因死亡风险显著更高。使用二甲双胍的男性数量相对较少是本研究的一个主要局限性。