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度他雄胺(一种双重 5α-还原酶抑制剂)对良性前列腺增生症患者血清睾酮和体重指数的影响。

Effect of the dual 5alpha-reductase inhibitor, dutasteride, on serum testosterone and body mass index in men with benign prostatic hyperplasia.

机构信息

Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea.

出版信息

BJU Int. 2010 Apr;105(7):970-4. doi: 10.1111/j.1464-410X.2009.08915.x. Epub 2009 Sep 29.

DOI:10.1111/j.1464-410X.2009.08915.x
PMID:19793378
Abstract

OBJECTIVE

To investigate the effects of dutasteride on serum testosterone level and body mass index (BMI) in men who received medical therapy for benign prostatic hyperplasia (BPH).

PATIENTS AND METHODS

In all, 120 patients with BPH were randomized to three treatment groups: tamsulosin 0.2 mg/day (alpha-blocker group), dutasteride 0.5 mg/day (dutasteride group), or tamsulosin 0.2 mg plus dutasteride 0.5 mg/day (combination group) for 1 year. For all patients the BMI and serum testosterone levels were checked at baseline and after 1 year of treatment.

RESULTS

Among the evaluable 107 patients, the dutasteride (33) and combination groups (37) had significantly greater increases in serum testosterone level (16.3% and 15%, respectively) than the alpha-blocker group (37; 0.3%) after 1 year of treatment (both P < 0.001). When analysed by baseline serum testosterone tertile, the increases in serum testosterone level among the dutasteride and combination group were greatest in the lowest tertile. For BMI, the dutasteride and combination group had mean decreases of 0.17 and 0.20 kg/m(2), respectively, at 1 year, whereas the alpha-blocker group had a mean increase of 0.04 kg/m(2). The decreases in BMI for the dutasteride and combination group were statistically significant only in the lowest tertile (P = 0.048 and 0.010, respectively).

CONCLUSION

Our results show that dutasteride treatment in men with BPH led to a significant increase in serum testosterone level and a significant decrease in BMI among those with relatively lower baseline serum testosterone levels.

摘要

目的

研究度他雄胺对接受良性前列腺增生(BPH)药物治疗的男性的血清睾酮水平和体重指数(BMI)的影响。

患者和方法

共 120 例 BPH 患者被随机分为三组治疗:坦索罗辛 0.2mg/天(α受体阻滞剂组)、度他雄胺 0.5mg/天(度他雄胺组)或坦索罗辛 0.2mg+度他雄胺 0.5mg/天(联合组),疗程 1 年。所有患者在基线和治疗 1 年后检查 BMI 和血清睾酮水平。

结果

在可评价的 107 例患者中,度他雄胺(33 例)和联合组(37 例)治疗 1 年后血清睾酮水平分别显著升高(分别为 16.3%和 15%),而 α受体阻滞剂组(37 例;0.3%)(均 P < 0.001)。按基线血清睾酮三分位值分析,度他雄胺和联合组的血清睾酮水平升高幅度在最低三分位值最大。BMI 方面,度他雄胺和联合组在 1 年内平均下降 0.17 和 0.20kg/m2,而 α受体阻滞剂组平均增加 0.04kg/m2。只有在最低三分位值时,度他雄胺和联合组的 BMI 下降有统计学意义(P = 0.048 和 0.010)。

结论

我们的结果表明,度他雄胺治疗 BPH 可导致血清睾酮水平显著升高,且基线血清睾酮水平较低的患者 BMI 显著降低。

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