Massively Parallel Sequencing-based Noninvasive Prenatal Detection of Fetal Sex Chromosome Aneuploid

来源 :中华医学会2012年医学遗传学年会暨全国第十一次医学遗传学学术会议 | 被引量 : 0次 | 上传用户:wqkabc0
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  Objectives To explore the accuracy of sex chromosome aneuploidy detection when clinically applied MPS-based noninvasive fetal aneuploidy test in Southwest hospital and investigate the accuracy of this method in noninvasive prenatal determination of fetal gender.Methods A large scale of clinical implementation was carried out in Southwest Hospital,the Third Military Medical University,Chongqing,China over a 12month period from June,2011 to June,2012.2251 pregnant women referred to outpatient clinic of Southwest hospital were recruited.All of them were ethnic Chinese with singleton pregnancies.Plasma cell free DNA was extracted from 5ml maternal peripheral blood and was prepared for massively parallel sequencing(MPS)by HiSeq2000.Then student t test and the estimation of fetal DNA concentration by sex chromosome are applied to distinguish sex chromosome aneuploidies.Meanwhile,fetal gender was classified by the representation of DNA from chromosome Y for all the samples before getting karyotyping results and follow-up results.Results In MPSbased noninvasive prenatal aneuploidy test,we totally detected out 46 cases with high risk of sex chromosome aneuploidy from all 2251 pregnant women(Positive Rate,2.04%).Among them,7 were tested out as high risk ofXO,5 of them were performed invasive procedure and 2 of them is confirmed,with a PPV(Positive Prediction Value)40.00%;9 cases as high risk ofXXX,6 of them were with karyotyping result and all of them were confirmed to be XXX with a PPV 100%(one of these cases is confirmed to be maternal XXX);Still there are 8 cases we reported as high risk of XXY,7 of them performed karyotyping testing,but only 3 of them is confirmed to be true XXY with a PPV 42.86%;We only detected out 3 XYY cases and 1 of them had accepted amniocentesis which is confirmed to be XYY already;In our earlier clinical application,we reported out 19 non-specific sex chromosome aneuploidy cases(with chromosome Y representation and with lower representation of chromosome X),but only one of them is confirmed to be 45,X,[16]/46,XY,[16] by amniocentesis and other 18 cases confirmed to be false positive with a PPV only 5.26% which showed this non-specific type is of poor prediction power and maybe unsuitable for reporting out in the future.In the gender classification analysis,1669 out of 1683 samples with confirmed gender information of kayotyping result or follow-up result was accurately classified(accuracy rate,99.17%).Conclusion:Our data demonstrates MPS-based noninvasive prenatal testing is an effective way to distinguish sex chromosome aneuploidies and could provide an outstanding additional support to genetic counseling.
其他文献
背景 输注血细胞和移植造血干细胞是细胞治疗的常用手段,可以用来治疗遗传性疾病、恶性血液病和重症免疫缺陷等多种疾病.造血系细胞也是采用ex vivo基因治疗策略的重要靶细胞.本研究组前期已经利用人核糖体基因区打靶载体(pHrneo)将人凝血因子IX(hFIX)靶入到人胚胎干细胞(human embryonic stem cells,hESCs)的rDNA区,因此将hESCs定向分化成造血系细胞,将为
目的 研究p53基因结合区域单核苷酸多态性(single nucleotide polymorphism,SNP)与中国汉族人群食管鳞状细胞癌(esophageal squamous cell carcinoma,ESCC)的相关性.方法 采用SnapShot的方法,对400例食管鳞状细胞癌患者和400例正常对照的人群的三个p53下游靶基因Bax、CDKN1A、GADD45A的6个SNPs rs1
A new class of non-coding RNAs,designated long non-coding RNAs(lncRNAs),was recently found to be frequently deregulated in various diseases.Although previous data suggested that lncRNAs are likely to
肥厚型心肌病(hypertrophic cardiomyopathy,HCM)是一种主要由心肌肌小节基因突变导致的常染色体显性遗传病,以无明显诱因下出现的以非对称性室间隔肥厚(≥13mm)为主的左室肥厚为主要表现,大多数患者无症状,预后良好,少数患者可同时出现黑朦、晕厥、心绞痛、心力衰竭及心源性猝死(sudden cardiac death,SCD),是青年人SCD的首要原因.心肌肌球蛋白结合蛋白
目的 MicroRNA-126定位于9q34.3,该区域在非小细胞肺癌(NSCLC)中经常缺失,在前期研究中,发现MicroRNA-126表达在NSCLC癌组织中显著低于癌旁组织;同时生物信息学分析发现其靶基因中有多个肿瘤相关基因.因此推测此miRNA表达下调或缺失可能导致其靶基因调控紊乱,参与了NSCLC发生、发展和转移.本研究旨在探讨MicroRNA-126对非小细胞肺癌肿瘤生长的作用及与非小
A new class of non-coding RNAs,designated long non-coding RNAs(lncRNAs),was recently found to be frequently deregulated in various diseases.Although previous data suggested that lncRNAs are likely to
会议
会议
目的 探讨人胰岛素样生长因子受体-1(IGF-1R)基因单核苷酸多态性(SNP)位点与特发性矮小(ISS)遗传易感性的关系.方法 选择788例ISS患儿(ISS组),572名身高正常人(对照组),用SNaPshot技术平台进行基因分型.结果 ①初筛后发现2个阳性位点rs1976667(P=0.03636)及rs2684788(P=0.01352)SNP位点与ISS有关;②扩大样本验证后发现,两个S
会议
It is widely accepted that aberrant DNA methylation at promoter regions commonly occurs in cancer cells and has been implicated in the epigenetic silencing of tumor suppressor genes.Here we demonstrat
Objective To report the application and accuracy ofMPS-based noninvasive fetal aneuploidy test in prenatal detection of fetal chromosomal aneuploidies in Southwest Hospital.Methods 2251 outpatient eth