Sen S, Ambulkar P, Hinduja I, Zaveri K, Gokral J, Pal A, Modi D
Molecular and Cellular Biology Laboratory, National Institute for Research in Reproductive Health (ICMR), J. M. Street, Parel, Mumbai, 400012, India.
Human Genetic Division, Department of Anatomy, Mahatma Gandhi Institute of Medical Sciences, Sevagram, 442102, Wardha, India.
J Assist Reprod Genet. 2015 Sep;32(9):1333-41. doi: 10.1007/s10815-015-0520-4. Epub 2015 Jul 7.
The purpose of this study was to determine the association of AZFc subdeletions (gr/gr, b1/b3 and b2/b3) and deletion of DAZ and CDY1 gene copies with male infertility
Three hundred twelve controls, 172 azoospermic and 343 oligozoospermic subjects were subjected to AZFc subdeletion typing by STS PCR. Deletion of DAZ and CDY1 gene copies was done using sequence family variant analysis. Sperm concentration and motility were compared between men with and without AZFc subdeletions. Effect of the AZFc subdeletions on ICSI outcome was evaluated.
Amongst the three AZFc subdeletions, the frequency of gr/gr was higher in oligozoospermic (10.5 %) and azoospermic (11.6 %) men as compared to controls (5.1 %). In men with AZFc subdeltions, loss of two DAZ and one CDY1 gene copy made them highly susceptible to azoospermia and severe oligozoospermia with OR of 29.7 and 26, respectively. These subdeletions had no effect on ICSI outcome, albeit there were an increased number of poor quality embryos in AZFc subdeleted group.
AZFc subdeletions are a major risk factor for male infertility in the Indian population. In the subjects with AZFc subdeletions, the deletion of DAZ and CDY1 gene copies increases its susceptibility to azoospermia or severe oligozoospermia. Since these deletions can be vertically transmitted to the future male offspring by ICSI, it will be essential to counsel the couples for the transmission of the genetic defect in the male offspring born after assisted reproduction and the risk of perpetuating infertility in future generation.
本研究旨在确定AZFc亚缺失(gr/gr、b1/b3和b2/b3)以及DAZ和CDY1基因拷贝缺失与男性不育的关联。
对312名对照者、172名无精子症患者和343名少精子症患者进行STS PCR检测以进行AZFc亚缺失分型。使用序列家族变异分析检测DAZ和CDY1基因拷贝的缺失情况。比较有无AZFc亚缺失男性的精子浓度和活力。评估AZFc亚缺失对卵胞浆内单精子注射(ICSI)结局的影响。
在三种AZFc亚缺失中,与对照组(5.1%)相比,少精子症男性(10.5%)和无精子症男性(11.6%)中gr/gr的频率更高。在患有AZFc亚缺失的男性中,两个DAZ基因拷贝和一个CDY1基因拷贝的缺失使他们极易患无精子症和严重少精子症,其比值比分别为29.7和26。这些亚缺失对ICSI结局无影响,尽管在AZFc亚缺失组中质量差的胚胎数量有所增加。
AZFc亚缺失是印度人群男性不育的主要危险因素。在患有AZFc亚缺失的受试者中,DAZ和CDY1基因拷贝的缺失增加了其患无精子症或严重少精子症的易感性。由于这些缺失可通过ICSI垂直遗传给未来的男性后代,因此必须为夫妇提供咨询,告知他们辅助生殖后出生的男性后代遗传缺陷的传递情况以及未来几代人不孕延续的风险。