Thanh Tung Nguyen, Tien Sang Trieu, Van Phong Nguyen, Thai Son Dang, Cong Thuc Luong, Le Tuan Dinh, Nguyen Son Tien, Van Tuan Tran, Duong Hoang Huy, Bui Tien Minh, Nguyen Kien Trung
Military Institute of Clinical Embryology and Histology, Vietnam Military Medical University, Hanoi, 100000, Vietnam.
Department of Biology and Medical Genetics, Vietnam Military Medical University, Hanoi, 100000, Vietnam.
Int J Gen Med. 2024 Apr 24;17:1579-1589. doi: 10.2147/IJGM.S455513. eCollection 2024.
To optimize the multiplex polymerase chain reaction (M-PCR) technique to diagnose microdeletions of azoospermia factors (AZF) on the Y chromosome and initially apply the technique to diagnose male patients with sperm density less than 5×10 million sperm/mL was assigned to do a test to check for AZF microdeletions on the Y chromosome.
Based on the positive control samples which belong to male subjects who have had 2 healthy children without any assisted reproductive technologies, the M-PCR method was developed to detect simultaneously and accurately AZF microdeletions on 32 male patients with sperm densities below 5×10 million sperm/mL of semen at the Department of Biology and Medical Genetics - Vietnam Military Medical University.
Successful optimization of the M-PCR technique including 7 reactions arranged according to each AZFabc region using 24 STS/gene on the Y chromosome. Initial application to diagnose AZF deletion on 32 azoospermic and oligospermic men reveals that AZFa deletion accounts for 6.25% (2/32); deletion of all 3 regions AZFa,b,c with 18.75% (6/32 cases); The combined deletion rate of AZFb,c is highest, accounting for 56.24% (18/32 patients).
Successfully optimized the M-PCR technique in identifying AZF microdeletions using 24 sequence tagged sites (STS)/gene for azoospermic and oligozoospermic men. The M-PCR technique has great potential in the application of AZF deletion diagnosis.
为优化多重聚合酶链反应(M-PCR)技术以诊断Y染色体上无精子症因子(AZF)的微缺失,并初步应用该技术对精子密度低于5×10⁶/mL的男性患者进行检测,以检查Y染色体上的AZF微缺失情况。
以生育2个健康孩子且未使用任何辅助生殖技术的男性为阳性对照样本,开发M-PCR方法,对越南军事医学大学生物与医学遗传学系32例精液精子密度低于5×10⁶/mL的男性患者同时准确检测AZF微缺失情况。
成功优化M-PCR技术,包括根据Y染色体上每个AZFabc区域安排7个反应,使用24个序列标签位点/基因。对32例无精子症和少精子症男性进行AZF缺失诊断的初步应用显示,AZFa缺失占6.25%(2/32);AZFa、b、c所有3个区域缺失占18.75%(6/32例);AZFb、c联合缺失率最高,占56.24%(18/32例患者)。
成功优化了M-PCR技术,使用24个序列标签位点(STS)/基因对无精子症和少精子症男性进行AZF微缺失鉴定。M-PCR技术在AZF缺失诊断应用中具有很大潜力。