Puah C M, Williams G, Ghanadian R
Urol Res. 1982;10(2):81-4. doi: 10.1007/BF00262407.
A sensitive and reliable radioimmunoassay (RIA) for urinary unconjugated 5 alpha-androstane-3 alpha, 17 beta-diol is described. The mean overall recovery of unconjugated 5 alpha-androstane-3 alpha, 17 beta-diol was found to be 57.4%. The sensitivity of the assay was 79 fmol per assay tube and the intra and inter-assay variations ranged between 7.2% and 11.4%. The mean +/- SEM for the concentration of this androgen in the urine of normal men was 339.6 +/- 66.8 nmol/24 h. The corresponding values for patients with benign prostatic hypertrophy (BPH) and carcinoma of the prostate (Ca) were 297.8 +/- 44.7 and 1592.1 +/- 622.7 respectively. The mean value for Ca patients was significantly higher than either BPH (p less than 0.05) or normal subject (p less than 0.02), suggesting a differential urinary excretion pattern for unconjugated 5 alpha-androstane-3 alpha, 17 beta-diol between BPH and Ca patients. It is concluded that the combined measurement of this androgen in the plasma and urine provides a more accurate assessment of the profile of this hormone than a single plasma estimation.
本文描述了一种用于检测尿中未结合的5α-雄甾烷-3α,17β-二醇的灵敏且可靠的放射免疫分析方法(RIA)。未结合的5α-雄甾烷-3α,17β-二醇的平均总回收率为57.4%。该分析方法的灵敏度为每管79飞摩尔,批内和批间变异范围在7.2%至11.4%之间。正常男性尿液中这种雄激素浓度的平均值±标准误为339.6±66.8纳摩尔/24小时。良性前列腺增生(BPH)患者和前列腺癌(Ca)患者的相应值分别为297.8±44.7和1592.1±622.7。Ca患者的平均值显著高于BPH患者(p<0.05)或正常受试者(p<0.02),这表明BPH患者和Ca患者之间未结合的5α-雄甾烷-3α,17β-二醇的尿排泄模式存在差异。结论是,与单次血浆估计相比,联合检测血浆和尿液中的这种雄激素能更准确地评估该激素的情况。