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投稿时间:2021-02-04 网络发布日期:2021-10-20
投稿时间:2021-02-04 网络发布日期:2021-10-20
中文摘要: 目的 探讨全外显子组测序(WES)检测技术在特发性重度少畸精子症中的临床意义。
方法 选取2019年1月至10月收治的54例特发性重度少畸精子症患者为研究对象,收集患者个人史、性激素等结果,采集全血标本进行WES检测,随访生育结局。
结果 54例患者中8例(14.81%)WES结果阳性,46例(85.19%)结果阴性;8例WES阳性病例共9种基因变异中的5种变异与临床表型一致,分别是SLC26A8、SPO11、DPY19L2、DNAH1和SUN5。WES阳性与WES阴性两组性激素水平、个人史方面差异无统计学意义( P >0.05)。随访中总体成功生育率37.04%(20/54),其中通过卵胞浆内单精子注射(ICSI)成功受孕率占80.00%(16/20)。总体不育率62.96%(34/54),其中受孕失败[包括自然流产和体外授精(IVF)失败]者占38.24%(13/34),仍在备孕者占61.76%(21/34),备孕者中拟行IVF者占71.43%(15/21)。
结论 WES检测为部分特发性重度少畸精子症患者提供了基因诊断依据。但临床治疗上,IVF仍是该类患者配偶成功受孕的主要方式。
Abstract:Objective To investigate the clinical significance of whole exome sequencing (WES) in severe idiopathic oligoasthenoteratozoospermia(iOAT).
Methods Fifty-four patients with severe iOAT treated from January to October 2019 were selected as the research subjects. After collecting the patients personal history, sex hormones and whole blood samples for WES detection, the patients were followed up for fertility outcomes. Results
There were WES-positive Results in 8 of 54 patients (14.81%)and WES-negative in 46 of 54 patients (85.19%). In WES-positive group, 5 out of 9 gene variants (SLC26A8, SPO11, DPY19L2, DNAH1 and SUN5) were consistent with the clinical phenotype. There were no significant differences in hormone levels and personal history between WES-positive group and WES-negative group ( P >0.05). During the follow-up period, the overall successful fertility rate was 37.04% (20/54), in which the successful pregnancy rate through intracytoplasmic sperm injection (ICSI) accounted for 80.00% (16/20). The overall infertility rate was 62.96% (34/54), in which spontaneous abortion and in vitro fertilization(IVF) failure accounted for 38.24% (13/34), and the persons still preparing for pregnancy were 61.76% (21/34). The persons proposed for IVF accounted for 72.43%(15/21).
Conclusions WES detection provides a basis for the genetic diagnosis of some severe iOAT patients. In clinical practice, IVF remains an effective option for successful pregnancy for the spouses of iOAT patients.
文章编号: 中图分类号: 文献标志码:A
基金项目:国家自然科学基金(81771572);十三五南京市卫生青年人才培养工程项目(QRX17071)
附件
引用文本:
潘锋,张兴源,潘连军.特发性重度少畸精子症全外显子组测序的临床意义[J].中国临床研究,2021,34(10):1314-1318.
潘锋,张兴源,潘连军.特发性重度少畸精子症全外显子组测序的临床意义[J].中国临床研究,2021,34(10):1314-1318.