Jayalath Viranda H, Ireland Christopher, Fleshner Neil E, Hamilton Robert J, Jenkins David J A
Clinical Nutrition and Risk Factor Modification Center, St. Michael's Hospital, Toronto, Ontario, Canada.
Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Prostate. 2016 Nov;76(15):1445-53. doi: 10.1002/pros.23228. Epub 2016 Jul 12.
Metformin is the first-line oral antihyperglycemic of choice for individuals with type 2 diabetes. Recent evidence supports a role for metformin in prostate cancer chemoprotection. However, whether metformin indeed influences prostate biology is unknown. We aimed to study the association between metformin and serum prostate-specific antigen (PSA) levels-the primary prostate cancer biomarker.
We conducted a cross-sectional study of 326 prostate cancer-free men with type 2 diabetes were recruited between 2004 and 2013 at St. Michael's Hospital. Men were excluded if they had a PSA ≥10-ng/ml, or used >2,550-mg/d metformin or supplemental androgens. Multivariate linear regressions quantified the association between metformin dose and log-PSA. Secondary analyses quantified the association between other antihyperglycemics (sulfonylureas, thiazolidinediones) and PSA; sensitivity analyses tested covariate interactions.
Median PSA was 0.9-ng/ml (IQR: 0.5-1.6-ng/ml). Metformin dose associated positively with BMI, HbA1c, diabetes duration, and number of statin, acetylsalicylic acid, diuretic users, and number of antihyperglycemics used, and negatively with LDL-C. In multivariate models, PSA changed by -8% (95%CI: -13 to -2%, P = 0.011) per 500-mg/d increase in metformin. Men with diabetes for ≥6 years (n = 163) saw a greater difference in PSA per 500-mg/d metformin (-12% [95% CI: -19 to -4%, P = 0.002], P-interaction = 0.018). Serum PSA did not relate with sulfonylureas, thiazolidinediones, or total number of antihyperglycemic agents used. Our findings are limited by the cross-sectional design of this study.
Metformin dose-dependently inversely associated with serum PSA, independent of other antihyperglycemic medications. Whether metformin confers a dose-dependent benefit on prostate tumorigenesis and progression warrants investigation. Prostate 76:1445-1453, 2016. © 2016 The Authors. The Prostate published by Wiley Periodicals, Inc.
二甲双胍是2型糖尿病患者的一线口服降糖药。近期证据支持二甲双胍在前列腺癌化学预防中发挥作用。然而,二甲双胍是否真的会影响前列腺生物学尚不清楚。我们旨在研究二甲双胍与血清前列腺特异性抗原(PSA)水平(前列腺癌的主要生物标志物)之间的关联。
我们对2004年至2013年期间在圣迈克尔医院招募的326名无前列腺癌的2型糖尿病男性进行了一项横断面研究。如果男性的PSA≥10 ng/ml,或使用超过2550 mg/d的二甲双胍或补充雄激素,则将其排除。多变量线性回归量化了二甲双胍剂量与log-PSA之间的关联。二次分析量化了其他降糖药(磺脲类、噻唑烷二酮类)与PSA之间的关联;敏感性分析测试了协变量相互作用。
PSA中位数为0.9 ng/ml(四分位间距:0.5 - 1.6 ng/ml)。二甲双胍剂量与BMI、糖化血红蛋白、糖尿病病程、他汀类药物、乙酰水杨酸、利尿剂使用者数量以及使用的降糖药数量呈正相关,与低密度脂蛋白胆固醇呈负相关。在多变量模型中,二甲双胍每增加500 mg/d,PSA下降8%(95%置信区间:-13%至-2%,P = 0.011)。糖尿病病程≥6年的男性(n = 163),二甲双胍每增加500 mg/d,PSA的差异更大(-12% [95%置信区间:-19%至-4%,P = 0.002],P相互作用 = 0.018)。血清PSA与磺脲类、噻唑烷二酮类或使用的降糖药总数无关。本研究的横断面设计限制了我们的研究结果。
二甲双胍剂量依赖性地与血清PSA呈负相关,独立于其他降糖药物。二甲双胍是否对前列腺肿瘤发生和进展具有剂量依赖性益处值得研究。《前列腺》76:1445 - 1453,2016年。© 2016作者。由威利期刊公司出版的《前列腺》