Suppr超能文献

接受睾酮替代疗法的性腺功能减退男性的前列腺特异性抗原变化与前列腺癌

Prostate-specific antigen changes and prostate cancer in hypogonadal men treated with testosterone replacement therapy.

作者信息

Coward Robert M, Simhan Jay, Carson Culley C

机构信息

Division of Urologic Surgery, The University of North Carolina, Chapel Hill, NC, USA.

出版信息

BJU Int. 2009 May;103(9):1179-83. doi: 10.1111/j.1464-410X.2008.08240.x. Epub 2008 Dec 23.

Abstract

OBJECTIVES

To retrospectively review hypogonadal men receiving testosterone replacement therapy (TRT), and evaluate the changes in prostate-specific antigen (PSA) levels over an extended period, and thus evaluate the occurrence of prostate cancer, as a primary concern in treating late-onset hypogonadism (LOH) is the potential increased risk of prostate cancer; we also recorded the cardiovascular effects of TRT.

PATIENTS AND METHODS

In all, 81 hypogonadal men (mean age 56.8 years) were followed for a mean (range) of 33.8 (6-144) months after starting TRT. All men had a normal baseline PSA level before TRT and had routine laboratory investigations, including measurements of body mass index (BMI), haematocrit, lipid profile, and liver function tests (LFTs). Testosterone and PSA levels were assessed every 6-12 months. Patients with a biopsy-confirmed or recent history of prostatitis before treatment were excluded. TRT was discontinued in men who developed prostate cancer.

RESULTS

Before and 36 months after treatment the total testosterone levels were 241.1 and 379.8 ng/dL (P < 0.05), respectively. Four men (4.9%) developed prostate cancer at a mean (range) of 32.5 (22-41) months after starting TRT. In men without prostate cancer (95.1%), PSA levels did not increase significantly at 1-year intervals for 5 years. There was no statistical difference in PSA level change from baseline to 36 months when patients without prostate cancer were stratified into groups according to age (< or =50, 55-65 and > or =70 years). In men with prostate cancer there was an increase in mean PSA level from baseline to 18 months of 1.8 ng/mL, and to 36 months of 3.2 ng/mL (P < 0.05). Total cholesterol improved from 203.8 to 166.6 mg/dL (P < 0.05) after 36 months of TRT; the BMI, haematocrit and LFTs did not change significantly.

CONCLUSIONS

LOH is an increasingly prevalent disease characterized by a symptomatically low testosterone level, and TRT is effective in normalizing serum testosterone levels, providing a beneficial cardiovascular effect, and improving sexual function and overall quality of life. PSA levels remain stable after normalization of testosterone for > or =5 years, prostate cancer can be effectively diagnosed and treated in men taking TRT, and the incidence of prostate cancer among men with LOH on TRT is no greater than that in the general population.

摘要

目的

回顾性研究接受睾酮替代疗法(TRT)的性腺功能减退男性,评估其前列腺特异性抗原(PSA)水平在较长时间内的变化,从而评估前列腺癌的发生情况,因为治疗迟发性性腺功能减退(LOH)时主要关注的是前列腺癌风险可能增加;我们还记录了TRT的心血管效应。

患者与方法

共有81例性腺功能减退男性(平均年龄56.8岁)在开始TRT后平均随访33.8(6 - 144)个月。所有男性在TRT前PSA水平正常,并进行了常规实验室检查,包括测量体重指数(BMI)、血细胞比容、血脂谱和肝功能检查(LFTs)。每6 - 12个月评估一次睾酮和PSA水平。排除治疗前活检确诊或近期有前列腺炎病史的患者。患前列腺癌的男性停止TRT。

结果

治疗前和治疗36个月后,总睾酮水平分别为241.1和379.8 ng/dL(P < 0.05)。4例男性(4.9%)在开始TRT后平均32.5(22 - 41)个月时患前列腺癌。在无前列腺癌的男性(95.1%)中,5年内PSA水平每年间隔无显著升高。将无前列腺癌的患者按年龄(≤50、55 - 65和≥70岁)分层后,从基线到36个月PSA水平变化无统计学差异。在患前列腺癌的男性中,从基线到18个月平均PSA水平升高1.8 ng/mL,到36个月升高3.2 ng/mL(P < 0.05)。TRT 36个月后总胆固醇从203.8降至166.6 mg/dL(P < 0.05);BMI、血细胞比容和LFTs无显著变化。

结论

LOH是一种日益普遍的疾病,其特征是睾酮水平有症状性降低,TRT可有效使血清睾酮水平正常化,具有有益的心血管效应,并改善性功能和总体生活质量。睾酮正常化≥5年后PSA水平保持稳定,接受TRT的男性中前列腺癌可有效诊断和治疗,接受TRT的LOH男性中前列腺癌的发病率不高于普通人群。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验