Tomasi Paolo A, Oates Robert, Brown Laura, Delitala Giuseppe, Page David C
Howard Hughes Medical Institute, Whitehead Institute, and Department of Biology, Massachusetts Institute of Technology, Cambridge, 02142, USA.
Clin Endocrinol (Oxf). 2003 Aug;59(2):214-22. doi: 10.1046/j.1365-2265.2003.01828.x.
The most frequent known genetic causes of severe oligospermia (< 5 million sperm/ml) or azoospermia in men are Klinefelter's syndrome (KS), and deletions in the Y chromosome long arm (Yq). We aimed to compare the function of the pituitary-testicular axis in patients with severe oligospermia or azoospermia, idiopathic or associated with Y chromosome deletions or Klinefelter's syndrome (KS) and in control subjects.
We studied 47 men with idiopathic oligo-azoospermia, 42 with Yq deletions (27 AZFc, 13 AZFb and two AZFa) and oligo-azoospermia, 14 with KS and 39 control subjects (total 143).
We analysed levels of FSH, inhibin-B, LH, free testosterone and oestradiol in all subjects, and we calculated indexes based on those hormones.
Inhibin-B levels were indistinguishable between patients with idiopathic and Y deletion-associated oligo-azoospermia, lowest in the Klinefelter's patients and highest in controls. FSH levels followed the reverse pattern: indistinguishable between patients with idiopathic and deletion-associated oligo-azoospermia, highest in Klinefelter's patients and lowest in controls. Oestradiol, free testosterone and the derived indeces were not different in subjects with Yq deletions compared to those with idiopathic oligo-azoospermia. Among the Yq-deleted patients, no measured or derived parameter differed between the subjects with AZFc deletion and those with AZFb deletion. When non-KS oligo-azoospermic patients were classified according to histology [Sertoli cell-only (SCO), n = 18 or non-Sertoli cell only (non-SCO), n= 18] and compared to KS patients, the hormonal pattern did not differ between SCO and non-SCO subjects, but levels in KS patients were significantly different for FSH, inhibin-B and the FSH/inhibin-B ratio. KS patients not only had lower inhibin-B than SCO and non-SCO oligo-azoospermic men, but also higher FSH levels for any given inhibin-B concentration.
Our data show that Y-deleted patients do not have a lesser impairment of Sertoli cell function than patients with idiopathic oligo-azoospermia, and support the concept that the main determinant of inhibin-B production is the germ cell mass. Also, our results suggest that one or more other factors, apart from inhibin-B, may contribute to increased pituitary secretion of FSH in KS patients.
男性严重少精子症(<500万精子/毫升)或无精子症最常见的已知遗传原因是克氏综合征(KS)以及Y染色体长臂(Yq)缺失。我们旨在比较严重少精子症或无精子症患者(特发性或与Y染色体缺失或克氏综合征相关)与对照者垂体-睾丸轴的功能。
我们研究了47例特发性少精子症-无精子症患者、42例Yq缺失(27例AZFc、13例AZFb和2例AZFa)合并少精子症-无精子症患者、14例KS患者以及39例对照者(共143例)。
我们分析了所有受试者的促卵泡激素(FSH)、抑制素B、促黄体生成素(LH)、游离睾酮和雌二醇水平,并基于这些激素计算指数。
特发性和Y缺失相关少精子症-无精子症患者的抑制素B水平无差异,在克氏综合征患者中最低,在对照者中最高。FSH水平呈现相反模式:特发性和缺失相关少精子症-无精子症患者之间无差异,在克氏综合征患者中最高,在对照者中最低。与特发性少精子症患者相比,Yq缺失患者的雌二醇、游离睾酮及衍生指数无差异。在Yq缺失患者中,AZFc缺失患者和AZFb缺失患者的任何测量参数或衍生参数均无差异。当非KS少精子症-无精子症患者根据组织学分类[仅支持细胞(SCO),n = 18或非仅支持细胞(非SCO),n = 18]并与KS患者比较时,SCO和非SCO受试者的激素模式无差异,但KS患者的FSH、抑制素B及FSH/抑制素B比值水平有显著差异。KS患者不仅抑制素B低于SCO和非SCO少精子症-无精子症男性,而且在任何给定的抑制素B浓度下FSH水平更高。
我们的数据表明,Y缺失患者的支持细胞功能损害并不比特发性少精子症患者轻,支持了抑制素B产生的主要决定因素是生殖细胞数量的概念。此外,我们的结果表明,除抑制素B外,一个或多个其他因素可能导致KS患者垂体FSH分泌增加。