Yannucci Jennifer, Manola Judi, Garnick Marc B, Bhat Gajanan, Bubley Glenn J
Beth Israel Deaconess Medical Center, Waltham, Massachusetts 02215, USA.
J Urol. 2006 Aug;176(2):520-5. doi: 10.1016/j.juro.2006.03.057.
Although prostate cancer specific mortality is decreasing, there is little effect on overall mortality in this population, suggesting the possibility of an increased risk of death from nonprostate cancer related causes. Androgen deprivation therapy could adversely affect cardiovascular health. We investigated changes in lipid and glucose during androgen deprivation therapy.
We performed an exploratory analysis of pooled data from 3 prospective clinical trials aimed at achieving medical castration by comparing the gonadotropin releasing hormone antagonist abarelix, the gonadotropin releasing hormone agonist leuprolide acetate and leuprolide acetate plus the antiandrogen bicalutamide. Most patients were treated in the neoadjuvant setting or because of biochemical recurrence. Fasting serum lipid, glucose and hemoglobin A1C were determined in 1,102 men at baseline, and on treatment days 85 and 169. In the current study men were categorized into 3 treatment groups according to the type of androgen deprivation therapy, that is leuprolide acetate, leuprolide acetate plus bicalutamide or abarelix, and statin therapy.
Significant increases in total cholesterol, triglyceride and high density lipoprotein-cholesterol were observed in patients on leuprolide acetate or abarelix but not in patients on leuprolide acetate plus bicalutamide. Consistent changes in low density lipoprotein-cholesterol were not detected. Increased total cholesterol was usually due to an increase in high density lipoprotein-cholesterol. Hemoglobin A1C increased from baseline to day 85 only and there were no significant changes in fasting glucose measurements. The type of androgen deprivation therapy did not affect these parameters.
Short-term androgen deprivation therapy affects serum lipid and hemoglobin A1C independent of statin therapy.
尽管前列腺癌特异性死亡率在下降,但该人群的总体死亡率几乎没有受到影响,这表明非前列腺癌相关原因导致的死亡风险可能增加。雄激素剥夺治疗可能会对心血管健康产生不利影响。我们研究了雄激素剥夺治疗期间血脂和血糖的变化。
我们对3项前瞻性临床试验的汇总数据进行了探索性分析,这些试验旨在通过比较促性腺激素释放激素拮抗剂阿巴瑞克、促性腺激素释放激素激动剂醋酸亮丙瑞林以及醋酸亮丙瑞林加抗雄激素比卡鲁胺来实现药物去势。大多数患者在新辅助治疗阶段接受治疗,或因生化复发而接受治疗。在1102名男性患者的基线期、治疗第85天和第169天测定空腹血脂、血糖和糖化血红蛋白A1C。在本研究中,根据雄激素剥夺治疗的类型,即醋酸亮丙瑞林、醋酸亮丙瑞林加比卡鲁胺或阿巴瑞克,以及他汀类药物治疗,将男性患者分为3个治疗组。
接受醋酸亮丙瑞林或阿巴瑞克治疗的患者总胆固醇、甘油三酯和高密度脂蛋白胆固醇显著升高,但接受醋酸亮丙瑞林加比卡鲁胺治疗的患者未出现这种情况。未检测到低密度脂蛋白胆固醇的一致变化。总胆固醇升高通常是由于高密度脂蛋白胆固醇升高所致。糖化血红蛋白A1C仅从基线期到第85天有所升高,空腹血糖测量无显著变化。雄激素剥夺治疗的类型不影响这些参数。
短期雄激素剥夺治疗会影响血脂和糖化血红蛋白A1C,且与他汀类药物治疗无关。