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日本特发性无精子症男性雄激素受体基因的CAG重复长度分析及突变筛查

CAG repeat length analysis and mutation screening of the androgen receptor gene in Japanese men with idiopathic azoospermia.

作者信息

Sasagawa I, Suzuki Y, Ashida J, Nakada T, Muroya K, Ogata T

机构信息

Department of Urology, Yamagata University School of Medicine, Japan.

出版信息

J Androl. 2001 Sep-Oct;22(5):804-8.

Abstract

Because androgens are required for normal spermatogenesis, we are investigating abnormalities in the androgen receptor as a possible cause of impaired spermatogenesis in patients with idiopathic male infertility. The CAG repeat length in exon 1 and mutations of the androgen receptor gene were studied in 30 men with idiopathic azoospermia and in 51 fertile men. In men with azoospermia, plasma luteinizing hormone (LH), follicle-stimulating hormone (FSH), and testosterone levels were measured and testicular biopsies were performed. The CAG repeat length ranged from 19 to 30 (mean 23.4 +/- 2.9) and from 17 to 28 (mean 23.7 +/- 3.2) in men with azoospermia and in controls, respectively. There was no significant difference between the 2 groups. In men with azoospermia, the Johnsen testicular biopsy score negatively correlated with plasma FSH (P < .01). However, the Johnsen testicular biopsy score did not correlate with plasma LH and testosterone levels. The CAG repeat length did not correlate with the Johnsen testicular biopsy score, or with plasma concentrations of LH, FSH, and testosterone. No abnormalities in the androgen receptor gene were detected. These facts suggest that the CAG repeat length and alterations in the androgen receptor gene are not associated with the etiology of idiopathic azoospermia.

摘要

由于雄激素是正常精子发生所必需的,我们正在研究雄激素受体异常,将其作为特发性男性不育患者精子发生受损的可能原因。我们对30名特发性无精子症男性和51名有生育能力的男性进行了雄激素受体基因第1外显子CAG重复序列长度及突变情况的研究。对无精子症男性测定了血浆黄体生成素(LH)、卵泡刺激素(FSH)和睾酮水平,并进行了睾丸活检。无精子症男性和对照组的CAG重复序列长度分别为19至30(平均23.4±2.9)和17至28(平均23.7±3.2)。两组之间无显著差异。在无精子症男性中,约翰森睾丸活检评分与血浆FSH呈负相关(P<.01)。然而,约翰森睾丸活检评分与血浆LH和睾酮水平无关。CAG重复序列长度与约翰森睾丸活检评分以及血浆LH、FSH和睾酮浓度均无相关性。未检测到雄激素受体基因异常。这些事实表明,CAG重复序列长度及雄激素受体基因改变与特发性无精子症的病因无关。

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