首页 | 本学科首页   官方微博 | 高级检索  
     

高通量测序技术检测孕早期自然流产绒毛样本染色体异常发生的Meta分析
引用本文:辛淑文,杨少哲,胥博,滕少侠,李荣香,付秀虹. 高通量测序技术检测孕早期自然流产绒毛样本染色体异常发生的Meta分析[J]. 现代检验医学杂志, 2021, 0(1): 38-43. DOI: 10.3969/j.issn.1671-7414.2021.01.010
作者姓名:辛淑文  杨少哲  胥博  滕少侠  李荣香  付秀虹
作者单位:(漯河市中心医院生殖医学与遗传中心,河南漯河 462000)
基金项目:河南省医学科技攻关计划联合共建项目(LHGJ20191418);漯河医学高等专科学校2020年度创新创业发展能力提升工程科研类项目(2020-LYZKYYB021)。
摘    要:目的 通过单组率的Meta分析,探索早期流产绒毛样本染色体异常发生情况.方法 以自然流产、高通量测序技术等为检索词在CNKI,Pubmed等相关中英文数据库等进行检索,筛选纳入高通量测序技术检测孕早期自然流产绒毛样本染色体异常发生情况的文献,采用Revman 4.3软件进行荟萃分析.结果 该研究共纳入12篇文献,723...

关 键 词:高通量测序  自然流产  染色体  Meta分析

Incidence of the Chromosomal Abnormality of the Early Abortion Villi Samples by the Next Generation Sequence:A Meta-Analysis
XIN Shu-wen,YANG Shao-zhe,XU Bo,TENG Shao-xia,LI Rong-xiang,FU Xiu-hong. Incidence of the Chromosomal Abnormality of the Early Abortion Villi Samples by the Next Generation Sequence:A Meta-Analysis[J]. Journal of Modern Laboratory Medicine, 2021, 0(1): 38-43. DOI: 10.3969/j.issn.1671-7414.2021.01.010
Authors:XIN Shu-wen  YANG Shao-zhe  XU Bo  TENG Shao-xia  LI Rong-xiang  FU Xiu-hong
Affiliation:(Center for Reproductive Medicine and Genetics of Luohe Central Hospital, Henan Luohe 462000, China)
Abstract:Objective To explore the incidence of the chromosomal abnormality of the early abortion villi samples using the next generation sequence with a Meta-analysis.Methods The CNKI,Pubmed and other related Chinese and English database were retrieved to screen the literature that included the incidence of the chromosomal abnormality of the early abortion villi samples using the high throughput sequencing.Revman 4.3 software was used for meta-analysis.Results A total of 12 articles were included in the analysis,which includes 723 early abortion villi samples.Meta-analysis showed that there were 477 samples of chromosomal abnormality in 723 early abortion villi samples,the overall abnormal rate was 68%(0.58~0.76),the incidence rates of chromosomal abnormal number were 50%(0.43~0.57),and the incidence rates of chromosomal segmental deletion or duplication was 16%(0.09~0.24).Conclusion The next generation sequence technology can be used as the key means to detect the abnormality chromosomal in these early abortion villi samples.The abnormality of chromosomal is an important cause of spontaneous abortion in early pregnancy.
Keywords:next generation sequence  spontaneous abortion  chromosome  meta-analysis
本文献已被 维普 等数据库收录!
点击此处可从《现代检验医学杂志》浏览原始摘要信息
点击此处可从《现代检验医学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号