Mascarenhas Mariano, Thomas Sumi, Kamath Mohan S, Ramalingam Ramya, Kongari Ann Marie, Yuvarani S, Srivastava Vivi M, George Korula
Leeds Centre for Reproductive Medicine, Seacroft Hospital, Leeds, United Kingdom.
Reproductive Medicine Unit, Christian Medical College and Hospital, Vellore, India.
J Hum Reprod Sci. 2016 Jul-Sep;9(3):187-193. doi: 10.4103/0974-1208.192065.
To estimate the prevalence of chromosomal abnormalities and Y chromosome microdeletion among men with azoospermia and severe oligozoospermia and its correlation with successful surgical sperm retrieval.
A prospective study in a tertiary level infertility unit.
In a prospective observation study, men with azoospermia and severe oligozoospermia (concentration <5 million/ml) attending the infertility center underwent genetic screening. Peripheral blood karyotype was done by Giemsa banding. Y chromosome microdeletion study was performed by a multiplex polymerase chain reaction.
The study group consisted of 220 men, 133 of whom had azoospermia and 87 had severe oligozoospermia. Overall, 21/220 (9.5%) men had chromosomal abnormalities and 13/220 (5.9%) men had Y chromosome microdeletions. Chromosomal abnormalities were seen in 14.3% (19/133) of azoospermic men and Y chromosome microdeletions in 8.3% (11/133). Of the 87 men with severe oligozoospermia, chromosomal abnormalities and Y chromosome microdeletions were each seen in 2.3% (2/87). Testicular sperm aspiration was done in 13 men and was successful in only one, who had a deletion of azoospermia factor c.
Our study found a fairly high prevalence of genetic abnormality in men with severe semen abnormalities and a correlation of genetic abnormalities with surgical sperm retrieval outcomes. These findings support the need for genetic screening of these men prior to embarking on surgical sperm retrieval and assisted reproductive technology intracytoplasmic sperm injection.
评估无精子症和严重少精子症男性中染色体异常及Y染色体微缺失的患病率及其与手术取精成功的相关性。
在一家三级不孕不育治疗中心进行的前瞻性研究。
在一项前瞻性观察研究中,前往不孕不育中心就诊的无精子症和严重少精子症(浓度<500万/毫升)男性接受了基因筛查。外周血核型分析采用吉姆萨染色法。Y染色体微缺失研究通过多重聚合酶链反应进行。
研究组由220名男性组成,其中133人患有无精子症,87人患有严重少精子症。总体而言,220名男性中有21人(9.5%)存在染色体异常,220名男性中有13人(5.9%)存在Y染色体微缺失。无精子症男性中染色体异常的发生率为14.3%(19/133),Y染色体微缺失的发生率为8.3%(11/133)。在87名严重少精子症男性中,染色体异常和Y染色体微缺失的发生率均为2.3%(2/87)。对13名男性进行了睾丸精子抽吸术,仅1人成功,该男性存在无精子症因子c缺失。
我们的研究发现,精液严重异常的男性中遗传异常的患病率相当高,且遗传异常与手术取精结果相关。这些发现支持在进行手术取精和辅助生殖技术胞浆内单精子注射之前,对这些男性进行基因筛查的必要性。