Tateno T, Sasagawa I, Ichiyanagi O, Ashida J, Nakada T, Saito H, Hiroi M
Department of Urology, Yamagata University School of Medicine, Japan.
Fertil Steril. 1999 Apr;71(4):746-9. doi: 10.1016/s0015-0282(98)00546-9.
To evaluate the occurrence of microdeletions of the Y chromosome involving the DAZ and YRRM genes in patients with Klinefelter's syndrome with and without spermatogenesis.
Controlled clinical study.
Yamagata University Hospital, Yamagata, Japan.
PATIENT(S): Patients with Klinefelter's syndrome with spermatogenesis (n = 1) and without spermatogenesis (n = 20) and a control group of men of proven fertility (n = 10).
INTERVENTION(S): Blood and semen sampling and testicular biopsy.
MAIN OUTCOME MEASURE(S): Semen analysis, polymerase chain reaction amplification of 32 DNA loci on the long arm of the Y chromosome involving the DAZ (deleted in azoospermia) and YRRM (Y chromosome ribonucleic acid recognition motif) genes, and measurement of plasma FSH, LH, and testosterone levels.
RESULT(S): No microdeletions of 32 loci were found in any of the patients with Klinefelter's syndrome, either with or without spermatogenesis. Plasma LH and FSH levels were abnormally high and testosterone levels were reduced in all the patients with Klinefelter's syndrome. American Society for Reproductive Medicine.)
CONCLUSION(S): Severe impairment of spermatogenesis in patients with Klinefelter's syndrome is not caused by microdeletions of the Y chromosome involving the DAZ and YRRM genes.
评估克氏综合征患者中涉及DAZ和YRRM基因的Y染色体微缺失情况,这些患者有或无精子发生。
对照临床研究。
日本山形县山形大学医院。
有精子发生的克氏综合征患者(n = 1)、无精子发生的克氏综合征患者(n = 20)以及已证实有生育能力的男性对照组(n = 10)。
采集血液和精液样本以及进行睾丸活检。
精液分析、对Y染色体长臂上涉及DAZ(无精子症缺失基因)和YRRM(Y染色体核糖核酸识别基序)基因的32个DNA位点进行聚合酶链反应扩增,以及测量血浆促卵泡激素、促黄体生成素和睾酮水平。
在有或无精子发生的克氏综合征患者中均未发现32个位点的微缺失。所有克氏综合征患者血浆促黄体生成素和促卵泡激素水平异常升高,睾酮水平降低。(美国生殖医学学会)
克氏综合征患者精子发生的严重受损并非由涉及DAZ和YRRM基因的Y染色体微缺失所致。