Gavilan M, Vivar C, Núñez V, Choque C, Guzmán M, Duarte C
BIOLINKS Laboratories, Research & Development Lab, Lima, Peru.
Niu Vida. Specialized Center for Assisted Reproduction, Lima, Peru.
Heliyon. 2023 Sep 18;9(10):e20221. doi: 10.1016/j.heliyon.2023.e20221. eCollection 2023 Oct.
Y chromosome Microdeletions are the second genetic cause of infertility in men. Despite its importance for infertility treatment, there is no previous research in Peru. The aim of this study was to determine the frequencies and characteristics of Y chromosome microdeletions in a group of men who sought infertility consultation at a specialized reproductive medicine center in Peru.
In this study, 201 semen samples were analyzed. The samples were obtained from Niu Vida's fertility program. Each seminal sample was analyzed according to the recommendations of the Laboratory Manual of the World Health Organization (WHO) 2010. A buccal swab and a 500 μL aliquot of seminal sample were used for the molecular study of Y chromosome microdeletions in each patient. The frequencies and the type of Y chromosome microdeletion in the AZFa, AZFb and AZFc regions were evaluated.
The prevalence of Y chromosome microdeletions in the AZF region was 6.45% in oligozoospermic and azoospermic patients, and a prevalence of 20% was observed specifically in azoospermic patients. No microdeletions of AZFb type were detected. A partial region microdeletion of AZFa was detected in a teratozoospermic patient with a normal sperm count.
The study represents the first report on the incidence of Y chromosome microdeletions in Peru. Our results indicate a high prevalence of microdeletions in azoospermic patients compared to similar studies. It is suggested to assess the presence of AZFa microdeletions and to evaluate additional genetic markers in this region to identify specific mutations that may cause impaired sperm production and male infertility in the Peruvian male population.
Y染色体微缺失是男性不育的第二大遗传原因。尽管其对不育治疗很重要,但秘鲁此前尚无相关研究。本研究的目的是确定在秘鲁一家专业生殖医学中心寻求不育咨询的一组男性中Y染色体微缺失的频率和特征。
在本研究中,分析了201份精液样本。这些样本来自牛维达生育计划。每份精液样本均按照世界卫生组织(WHO)2010年《实验室手册》的建议进行分析。对每位患者,使用口腔拭子和500μL精液样本等分试样进行Y染色体微缺失的分子研究。评估了AZFa、AZFb和AZFc区域中Y染色体微缺失的频率和类型。
在少精子症和无精子症患者中,AZF区域Y染色体微缺失的患病率为6.45%,在无精子症患者中尤其观察到20%的患病率。未检测到AZFb型微缺失。在一名精子计数正常的畸形精子症患者中检测到AZFa的部分区域微缺失。
该研究是秘鲁关于Y染色体微缺失发生率的首份报告。我们的结果表明,与类似研究相比,无精子症患者中微缺失的患病率较高。建议评估AZFa微缺失的存在,并评估该区域的其他遗传标记,以确定可能导致秘鲁男性人群精子生成受损和男性不育的特定突变。