Cinar Ciğdem, Yazici Cenk, Ergünsu Sebnem, Beyazyürek Cağri, Javadova Dilara, Sağlam Yaman, Tarcan Tufan, Güney Ahmet Ilter
Department of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
Genet Test. 2008 Jun;12(2):195-202. doi: 10.1089/gte.2007.0056.
Infertile men having numerical or structural sperm defects may carry several genetic abnormalities (karyotype abnormalities, Y chromosome microdeletions, cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations, androgen receptor gene mutations, and abnormalities seen in sperm cells) leading to this situation. First we aimed to investigate the relationship between the numerical and constitutional (morphological) sperm anomalies and the genetic disorders that can be seen in infertile males. Our other aim was to compare two different kinds of kits that we use for the detection of Y chromosome microdeletions. Sixty-three infertile males [44 nonobstructive azoospermic, 8 severe oligozoospermic, and 11 oligoasthenoteratozoospermic] were investigated in terms of somatic chromosomal constitutions and microdeletions of the Y chromosome. Sperm aneuploidy levels were analyzed by fluorescence in situ hybridization (FISH) in sperm cells obtained from the semen of six OAT patients. Microdeletion and sex chromosome aneuploidy (47,XXY) rates in somatic cells were found to be approximately 3.2% and 4.7%, respectively. Sperm aneuploidy rates were determined as 9%, 22%, and 47% in three patients out of six. Two of these three patients also had high rates of head anomalies in semen samples. High correlation was found between sperm aneuploidy rates and sperm head anomalies. Since the introduction of the assisted reproductive techniques for the treatment of severe male infertility, genetic tests and genetic counseling became very important due to the transmission of genetic abnormalities to the next generation. Thus in a very near future, for a comprehensive male infertility panel, it will be essential to include additional genetic tests, such as CFTR gene mutations, sperm mitochondrial DNA mutations, and androgen receptor gene mutations, besides the conventional chromosomal analyses, Y chromosome microdeletion detection, and sperm-FISH analyses.
患有精子数量或结构缺陷的不育男性可能存在多种导致这种情况的基因异常(核型异常、Y染色体微缺失、囊性纤维化跨膜传导调节因子(CFTR)基因突变、雄激素受体基因突变以及精子细胞中出现的异常)。首先,我们旨在研究精子数量和形态异常与不育男性中可见的基因疾病之间的关系。我们的另一个目标是比较用于检测Y染色体微缺失的两种不同试剂盒。对63名不育男性[44例非梗阻性无精子症、8例严重少精子症和11例少弱畸精子症]进行了体细胞染色体构成和Y染色体微缺失方面的研究。通过荧光原位杂交(FISH)分析了从6例少弱畸精子症患者精液中获取的精子细胞中的精子非整倍体水平。发现体细胞中的微缺失和性染色体非整倍体(47,XXY)率分别约为3.2%和4.7%。6例患者中有3例的精子非整倍体率分别确定为9%、22%和47%。这3例患者中有2例精液样本中的头部异常率也很高。发现精子非整倍体率与精子头部异常之间存在高度相关性。自从引入辅助生殖技术治疗严重男性不育以来,由于基因异常会传递给下一代,基因检测和遗传咨询变得非常重要。因此,在不久的将来,对于全面的男性不育检测,除了传统的染色体分析、Y染色体微缺失检测和精子FISH分析外,纳入额外的基因检测,如CFTR基因突变、精子线粒体DNA突变和雄激素受体基因突变将至关重要。