摘要
目的探讨Y染色体无精子因子（azoospennia factor，AZF）区域微缺失与原发无精、严重少精症之间的关系。方法采用多重聚合酶链反应技术对广州地区103例原发无精子症、72例原发严重少精症患者及60名正常生育男性进行AZFa、AZFb、AZFc3个区域微缺失分析。结果60名正常生育男性未发现Y染色体AZF区域微缺失，175例生精障碍患者中发现AZF微缺失19例，总缺失率为10．9％。其中11例无精症患者和4例少精症患者的缺失发生在AZFc区域，缺失率为8．6％；1例无精症患者和2例少精症患者发生AZFb、AZFc双重缺失，缺失率为1．7％；1例无精症患者发生AZFa、b、c3个区域同时微缺失，缺失率0．6％。生精障碍组与正常生育男性组比较Y染色体AZF区域微缺失率差异具有统计学意义（P〈0．01）。结论Y染色体AZF区域微缺失是引起男性无精、少精子症的重要原因之一，对原发无精、少精子症患者在单精子注射之前进行微缺失筛查是必要的。
Objective To investigate the relationship between microdeletion of azoospennia factor （AZF） and male infertility. Methods Multiplex PCR was used to detect Y chromosome microdeletion in AZFa, AZFb and AZFc in 103 cases of idiopathic azoospemfia, 72 cases of severe idiopathic oligozoospemfia, and 60 healthy male controls. Results No microdeletion was found in 60 controls. Y chromosome microdeletion was found in 19 of 175 azoospemfia patients, the total prevalence rate of microdeletion was 10.9%. There were 15 cases （11 for azoospemfia, 4 for severe oligozoospemfia） in AZFc （8.6%）, 3 cases （1 for azoospemfia, 2 for severe oligozoospennia） in AZFb＋ c （1.7%）, 1 case （azoospemfia） in AZFa ＋ b ＋ c （0.6%）. According to statistics, the difference of microdeletion rate between two groups was significant（ P 〈 O. O1 ）. Conclusion Y chromosome microdeletions is an important mason of azoospemfia. Screening of Y chromosome microdeletions for azoospemfia patients before intracytoplasmic sperm injection treatment is essential.
出处
《中华医学遗传学杂志》
CAS
CSCD
北大核心
2007年第5期564-566,共3页
Chinese Journal of Medical Genetics
基金
2004广东省自然科学博士启动基金（04300344）
关键词
无精子因子
微缺失
男性不育
azoospennia factor
microdeletion
male infertility
