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首页> 外文期刊>BJU international >Prostate-specific antigen changes and prostate cancer in hypogonadal men treated with testosterone replacement therapy.
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Prostate-specific antigen changes and prostate cancer in hypogonadal men treated with testosterone replacement therapy.

机译:睾丸激素替代疗法治疗性腺功能减退男性的前列腺特异性抗原变化和前列腺癌。

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摘要

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.
机译:目的:回顾性研究接受睾丸激素替代疗法(TRT)的性腺功能减退的男性,并评估长期以来前列腺特异性抗原(PSA)水平的变化,从而评估前列腺癌的发生,将其作为治疗晚期肝癌的主要关注因素性腺功能减退症(LOH)是可能增加前列腺癌的风险;我们还记录了TRT对心血管的影响。患者与方法:总共81例性腺功能减退男性(平均年龄56.8岁)接受了TRT治疗后平均(范围)为33.8(6-144)个月。所有男性在接受TRT治疗前均具有正常的PSA基线水平,并进行了常规实验室检查,包括体重指数(BMI),血细胞比容,脂质分布和肝功能测试(LFT)的测量。每6-12个月评估一次睾丸激素和PSA水平。治疗前经活检证实或近期有前列腺炎病史的患者被排除在外。在患有前列腺癌的男性中停用TRT。结果:治疗前和治疗后36个月的总睾丸激素水平分别为241.1和379.8 ng / dL(P <0.05)。开始TRT后,四名男性(4.9%)患前列腺癌的平均时间(范围)为32.5(22-41)个月。在没有前列腺癌的男性中(95.1%),PSA水平在5年内以1年间隔没有显着增加。当没有前列腺癌的患者按年龄(<或= 50、55-65和>或= 70岁)分组时,从基线到36个月的PSA水平变化无统计学差异。在患有前列腺癌的男性中,平均PSA水平从基线增加到18个月时为1.8 ng / mL,增加到36个月时为3.2 ng / mL(P <0.05)。 TRT治疗36个月后,总胆固醇从203.8毫克/分升提高到166.6毫克/分升(P <0.05); BMI,血细胞比容和LFTs没有明显变化。结论:LOH是一种越来越普遍的疾病,其特征是睾丸激素水平低,而TRT可以有效地使血清睾丸激素水平正常化,提供有益的心血管作用,并改善性功能和整体生活质量。睾丸激素正常化≥5年后,PSA水平保持稳定,接受TRT的男性可以有效地诊断和治疗前列腺癌,接受TRT的LOH男性中前列腺癌的发生率不高于一般人群。

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