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NIPT技术介入临床检测后产前筛查与诊断唐氏儿的临床资料变化分析 被引量:2

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摘要 目的分析Noninvasive Prenatal Test(NIPT)技术是否可以替代所有血清学唐氏综合征的筛查以及其使用前景。方法比较首都医科大学附属北京妇产医院NIPT技术介入临床检测前后产前筛查与诊断的有关唐氏儿临床资料数据的变化。结果(2011年NIPT技术开始出现在部分孕妇中)2009年羊水穿刺总数2 262例,21-三体16例,诊断率0.7%,2010年羊水穿刺总数2 396例,21-三体18例,诊断率0.8%,2013年羊水穿刺总数2 179例,21-三体76例,诊断率3.5%,有62例外来NIPT结果为21-三体高风险的孕妇,经羊水穿刺核型分析结果为21-三体的是59例。2014年羊水穿刺总数2549例,21-三体69例,诊断率2.7%,有47例外来NIPT结果为21-三体的高风险者,经核型分析诊断后结果为21-三体者45例。结论 NIPT技术将大幅度改变羊水穿刺比例数,成为近乎诊断水平的唐氏儿筛查技术。
出处 《中国妇产科临床杂志》 CSCD 北大核心 2015年第5期457-458,共2页 Chinese Journal of Clinical Obstetrics and Gynecology
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参考文献10

  • 1刘子建,梁德杨,陈敏,廖灿.唐氏综合征的产前筛查模式和临床应用[J].中华妇产科杂志,2010,45(6):473-476. 被引量:19
  • 2Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and semm. Lancet, 1997, 350: 485-487.
  • 3Jackson L, Pyeritz RE. Molecular technologies open newclinical genetic vitas. Sci. Transl. Med, 2011, 3: 65ps2.
  • 4Burgess DJ. Human Disease: Next-generation sequencing of the next generation. Nat. Rev Genet, 2011, 12: 78.
  • 5Dan S, Chen F, Choy KW, et al. Prenatal detection of aneuploidy and imbalanced chromosomal arrangements by massively parallel sequencing. PloS one, 2012, 7: e27835.
  • 6Dan S, Wang W, Ren J, et al. Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11, 105 pregnancies with mixed risk factors. Prenatal diagnosis, 2012, 32: 1225-1232.
  • 7Zhou Q, Pan L, Chen S, et al. Clinical application of noninvasive prenatal testing for the detection of trisomies 21, 18, and 13 : a hospital experience. Prenatal diagnosis, 2014, 34: 1061-1065.
  • 8山丹,朱玄,玄兆伶,苏跃.孕妇外周血中胎儿DNA在唐氏综合征产前诊断的应用前景[J].中国妇产科临床杂志,2012,13(3):235-237. 被引量:1
  • 9Zhang H, Gao Y, Jiang F, et al. Non-invasive Prenatal Testing for Trisomy 21, 18 and 13: Clinical Experience from 146, 958 Pregnancies. Ultrasound Obstet Gynecol, 2015, 45 : 530-538.
  • 10Yao H, Jiang F, Hu H, et al. Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA : initial experience in a Chinese hospital. Ultrasound Obstet Gynecol, 2014, 44: 17-24.

二级参考文献53

  • 1Kornman LH,Morssink LP,Beekhuis JR,et al.Nuchal translucency cannot be used as a screening test for chromosomal abnormalities in the first trimester of pregnancy in a routine ultrasound practice.Prenat Diagn,1996,16:797-805.
  • 2Monni G,Zoppi MA,Ibba RM,et al.Fetal nuchal translucency test for Down's syndrome.Lancet,1997,350:1631-1632.
  • 3Timor-Tritsch IE,Fuchs KM,Monteagudo A,et al.Performing a fetal anatomy scan at the time of first-trimester screening.Obstet Gynecol,2009,113:402-407.
  • 4Atzei A,Gajewska K,Huggon IC,et al.Relationship between nuchal translucency thickness and prevalence of major cardiac defects in fetuses with normal karyotype.Ultrasound Obstet Gynecol,2005,26:154-157.
  • 5Hadlow NC,Hewitt BG,Dickinson JE,et al.Community-based screening for Down's syndrome in the first trimester using ultrasound and maternal serum biochemistry.BJOG,2005,112:1561-1564.
  • 6Wφjdemann KR,Shalmi AC,Chrisfiansen M,et al.Improved first-trimester Down syndrome screening performance by lowering the false-positive rate:a prospective study of 9941 low-risk women.Ultrasound Obstet Gyneeol,2005,25:227-233.
  • 7Leung TY,Chan LW,Law LW,et al.First trimester combined screening for Trisomy 21 in Hong Kong:outcome of the first 10,000 cases.J Matem Fetal Neonatal Med,2009,22:300-304.
  • 8Stenhouse EJ,Crossley JA,Aitken DA,et al.First-trimester combined ultrasound and biochemical screening for Down syndrome in rourine clinical practice.Prenat Diagn,2004,24:774-780.
  • 9Avgidou K,Papageorghiou A,Bindra R,et al.Prospective first-trimester screening for trisomy 21 in 30,564 pregnancies.Am J Obstet Gynecol,2005,192:1761-1767.
  • 10Cicero S,Spencer K,Avgidou K,et al.Maternal serum biochemistry at 11-13(+6) weeks in relation to the presence or absence of the fetal nasal bone on ultrasonography in chromosomally abnormal fetuses:an updated analysis of integrated ultrasound and biochemical screening.Prenat Diagn,2005,25:977 -983.

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