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首页> 外文期刊>Annals of laboratory medicine. >Evaluation of a Multiplex PCR Kit Used for Detecting Y Chromosome Microdeletions
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Evaluation of a Multiplex PCR Kit Used for Detecting Y Chromosome Microdeletions

机译:用于检测Y染色体微缺失的多重PCR试剂盒的评估

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Background : In addition to Klinefelter’s syndrome, microdeletion of Yq is the most common genetic cause of male infertility; 15% of azoospermic or 5-10% of oligozoospermic males have Yq deletions. We evaluated a Yq microdeletion kit (LG Life Sciences, Korea) for identifying microdeletions in the azoospermic factor (AZF) regions of the Yq. Methods : The kit was designed to amplify 3 regions of the AZF gene (AZFa, AZFb, and AZFc) using 15 sequence-tagged sites. We evaluated the preclinical performance of the kit. For clinical validation, 58 patients including 25 idiopathic azoospermic or oligozoospermic patients were examined. Results : We observed clear bands on electrophoresis of DNA, up to a DNA concentration of 3.12 ng/mL; the known microdeletion regions of all 6 reference cell-lines (Coriell, USA) were accurately detected and no false positiveegative results showed with normal female (n=11) and fertile male (n=15) specimens. This kit could identify the same microdeletions in the common regions, similar to another commercial kit. Among the 58 male infertile patients, 7 (12.1%) had microdeletions of the Yq. Among the idiopathic azoospermic (n=22) and oligozoospermic (n=3) patients, 3 (12.0%) had microdeletions. Further, 2 of 21 varicocele patients (9.5%), 1 of 4 patients with testicular failure, and 1 patient with a 45,X/46,XY mosaic had microdeletions. Conclusions : The kit was effective for detecting microdeletions of the Yq. We identified microdeletions in 12% of the infertile patients. This Y chromosome microdeletion detection kit is useful for screening Yq microdeletions in infertile patients.
机译:背景:除克氏综合征外,Yq的微缺失是男性不育的最常见遗传原因。 15%的无精子症男性或5-10%的少精子症男性具有Yq缺失。我们评估了Yq微缺失试剂盒(韩国LG生命科学),以鉴定Yq的无精子因子(AZF)区域中的微缺失。方法:该试剂盒经设计可使用15个带有序列标签的位点扩增AZF基因的3个区域(AZFa,AZFb和AZFc)。我们评估了该试剂盒的临床前性能。为了临床验证,检查了58例患者,包括25例特发性无精症或少精症患者。结果:我们在DNA电泳中观察到清晰的条带,最高DNA浓度为3.12 ng / mL。准确检测了所有6种参考细胞系(美国科里尔)的已知微缺失区域,正常雌性(n = 11)和可育雄性(n = 15)标本没有假阳性/阴性结果。该试剂盒可以识别共同区域中的相同微缺失,类似于另一种商用试剂盒。在58例男性不育患者中,有7例(12.1%)具有Yq微缺失。在特发性无精子症(n = 22)和少精子症(n = 3)患者中,3例(12.0%)有微缺失。此外,21例精索静脉曲张患者中有2例(9.5%),睾丸衰竭4例中的1例,45,X / 46,XY镶嵌有1例具有微缺失。结论:该试剂盒可有效检测Yq的微量缺失。我们在12%的不育患者中发现了微缺失。这种Y染色体微缺失检测试剂盒可用于筛选不育患者的Yq微缺失。

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