Sexual Medicine and Andrology Unit, Department of Clinical Physiopathology, University of Florence, Italy.
Andrology. 2013 Sep;1(5):764-71. doi: 10.1111/j.2047-2927.2013.00114.x.
Although in females of infertile couples abnormal prolactin (PRL) has a definitive role in the medical flowchart, its role in males is less clear. Animal models suggest that PRL does not play a major role in male reproduction, although its trophic action on male accessory glands was often observed. Studies in humans are scanty. We systematically evaluated possible clinical and ultrasound correlates of PRL in males of infertile couples. Of 288 consecutive males of infertile couples, 269 (36.6 ± 4.4 years) without genetic abnormalities were studied. All men underwent physical, biochemical, seminal evaluation and scrotal and transrectal ultrasound before and after ejaculation. Ejaculatory and erectile functions were assessed by Premature Ejaculation Diagnostic Tool (PEDT) and International Index of Erectile Function (IIEF)-15 respectively; prostate-related symptoms by National Institutes of Health-Chronic Prostatitis Symptom Index and International Prostate Symptom Score; psychological symptoms by Middlesex Hospital Questionnaire. Among semen parameters, only the positive association between PRL and ejaculate volume was significant, even adjusting for age, total testosterone and thyroid-stimulating hormone (adj. r = 0.126, p < 0.05). In a logistic ordinal model, adjusting for the aforementioned confounders and ejaculate volume, PRL was negatively associated with delaying ejaculation according to PEDT#1 score (Wald = 4.65, p < 0.05). In an age- and ejaculate volume-adjusted, iterative binary logistic model, low PRL was associated with a fivefold risk of any failure in controlling ejaculation (HR = 5.15 [1.15-23], p < 0.05). Among scrotal and transrectal ultrasound features, we found a significant positive association between PRL and seminal vesicles (SV) volume and inhomogeneity, before and after ejaculation, and with deferential ampullas diameter. Associations with PRL were confirmed in nested 1 : 1 case-control analysis. No significant associations were found between PRL and other clinical parameters. For the first time, this study extends the concept of a trophic effect of PRL on male accessory glands from animals to humans. We report a positive association among PRL and ejaculate and SV volume, before and after ejaculation. Low PRL is associated with a lessened ability to control ejaculation.
尽管在不孕夫妇的女性中,异常的催乳素(PRL)在医学流程图中具有明确的作用,但在男性中的作用尚不明确。动物模型表明,PRL 对男性生殖没有主要作用,尽管它对男性附属性腺的营养作用经常被观察到。人类的研究很少。我们系统地评估了 PRL 在不孕夫妇男性中的可能临床和超声相关性。在 288 名连续的不孕夫妇男性中,研究了 269 名(36.6±4.4 岁)无遗传异常的男性。所有男性在射精前和射精后都进行了体格检查、生化检查、精液评估以及阴囊和经直肠超声检查。射精和勃起功能分别通过早泄诊断工具(PEDT)和国际勃起功能指数(IIEF)-15 进行评估;前列腺相关症状通过美国国立卫生研究院-慢性前列腺炎症状指数和国际前列腺症状评分进行评估;心理症状通过米德尔塞克斯医院问卷进行评估。在精液参数中,只有 PRL 与精液量之间的正相关关系具有统计学意义,即使在调整年龄、总睾酮和促甲状腺激素后也是如此(调整后 r=0.126,p<0.05)。在逻辑有序模型中,在调整上述混杂因素和精液量后,PRL 与 PEDT#1 评分的延迟射精呈负相关(Wald=4.65,p<0.05)。在年龄和精液量调整的迭代二项逻辑模型中,低 PRL 与任何控制射精失败的风险增加五倍相关(HR=5.15[1.15-23],p<0.05)。在阴囊和经直肠超声特征中,我们发现 PRL 与射精后和射精前的精囊(SV)体积和不均匀性以及差异管直径之间存在显著正相关。在嵌套的 1:1 病例对照分析中证实了与 PRL 的相关性。PRL 与其他临床参数之间无显著相关性。这项研究首次将 PRL 对男性附属性腺的营养作用从动物扩展到人类。我们报告了 PRL 与精液和 SV 体积之间的正相关关系,包括射精前后。低 PRL 与控制射精的能力降低有关。