Li Quan, Song Ning-Hong, Cao Wen-Zhou, Shao Qiang, Xie Jian-Jun, Liu Chao, Wang Ya-Min, Shen Hua
Department of Urology, Suzhou Municipal Hospital Affiliated to Nanjing Medical University, 16 Baita Road, Suzhou, 215001 China.
Department of Urology, First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029 China.
Springerplus. 2016 Oct 18;5(1):1805. doi: 10.1186/s40064-016-3512-7. eCollection 2016.
The AZFc deletion has been associated with wide range of phenotypes including complete absence of germ cells in the testes (SCOS), reduction in germ cells hypospermatogenesis, and maturation arrest. The main objective of this study was to evaluate the relationship between AZFc microdeletions and testicular histology in South Chinese men with azoospermia or severe oligospermia.
338 men presenting with idiopathic non-obstructive azoospermia or severe oligospermia were evaluated between March 2012 and April 2015. Thirty-nine of the patients examined had an AZFc deletion (10.9 %). Testicular cytopathology was examined in 25 patients with an AZFc microdeletion and 14 with an AZFc deletion. There was no significant difference in the testicular histology of patients with partial or complete AZFc deletions (Mann-Whitney U = 152.500, p = 0.515). There was an association between testicular histology and gr/gr, b1/b3 or b2/b3 deletion (Fisher's exact test, p = 0.013).
Men with a gr/gr partial deletion were at higher risk of having hypospermatogenesis or maturation arrest. Men with a b1/b3 partial deletion were at higher risk of having maturation arrest. Men with a b2/b3 partial deletion were at higher risk of having maturation arrest or complete absence of germ cells in the testes.
AZFc缺失与多种表型相关,包括睾丸中完全没有生殖细胞(唯支持细胞综合征)、生殖细胞减少导致精子发生减少以及成熟停滞。本研究的主要目的是评估中国南方无精子症或严重少精子症男性中AZFc微缺失与睾丸组织学之间的关系。
在2012年3月至2015年4月期间对338例特发性非梗阻性无精子症或严重少精子症男性进行了评估。其中39例患者存在AZFc缺失(10.9%)。对25例AZFc微缺失患者和14例AZFc缺失患者进行了睾丸细胞病理学检查。部分或完全AZFc缺失患者的睾丸组织学无显著差异(曼-惠特尼U检验=152.500,p=0.515)。睾丸组织学与gr/gr、b1/b3或b2/b3缺失之间存在关联(费舍尔精确检验,p=0.013)。
gr/gr部分缺失的男性发生精子发生减少或成熟停滞的风险较高。b1/b3部分缺失的男性发生成熟停滞的风险较高。b2/b3部分缺失的男性发生成熟停滞或睾丸中完全没有生殖细胞的风险较高。