用户名: 密码: 验证码:
Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
详细信息    查看全文
  • 作者:Fuman Jiang (1)
    Jinghui Ren (2)
    Fang Chen (1)
    Yuqiu Zhou (3)
    Jiansheng Xie (4)
    Shan Dan (5)
    Yue Su (5)
    Jianhong Xie (3)
    Baomin Yin (3)
    Wen Su (3)
    Huakun Zhang (4)
    Wei Wang (1)
    Xianghua Chai (1)
    Linhua Lin (2)
    Hui Guo (2)
    Qiyun Li (2)
    Peipei Li (1)
    Yuying Yuan (1)
    Xiaoyu Pan (1)
    Yihan Li (1)
    Lifu Liu (1)
    Huifei Chen (1)
    Zhaoling Xuan (1)
    Shengpei Chen (1)
    Chunlei Zhang (1)
    Hongyun Zhang (1)
    Zhongming Tian (1)
    Zhengyu Zhang (1)
    Hui Jiang (1)
    Lijian Zhao (1)
    Weimou Zheng (1)
    Songgang Li (1)
    Yingrui Li (1)
    Jun Wang (1)
    Jian Wang (1)
    Xiuqing Zhang (1)
  • 关键词:Noninvasive Fetal Trisomy (NIFTY) test ; Massively parallel sequencing ; Autosomal aneuploidies ; Sex chromosomal aneuploidies
  • 刊名:BMC Medical Genomics
  • 出版年:2012
  • 出版时间:December 2012
  • 年:2012
  • 卷:5
  • 期:1
  • 全文大小:621KB
  • 参考文献:1. Driscoll DA, Gross S: Clinical practice. Prenatal screening for aneuploidy. / N Engl J Med 2009,360(24):2556-562. CrossRef
    2. Bouchlariotou S, Tsikouras P, Dimitraki M, Athanasiadis A, Papoulidis I, Maroulis G, Liberis A, Liberis V: Turner’s syndrome and pregnancy: has the 45, X/47, XXX mosaicism a different prognosis? Own clinical experience and literature review. / J Matern Fetal Neonatal Med 2011,24(5):668-72. CrossRef
    3. Leggett V, Jacobs P, Nation K, Scerif G, Bishop DV: Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review. / Dev Med Child Neurol 2010,52(2):119-29. CrossRef
    4. Hofherr SE, Wiktor AE, Kipp BR, Dawson DB, Van Dyke DL: Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience. / J Assist Reprod Genet 2011,28(11):1091-098. CrossRef
    5. Rives N, Simeon N, Milazzo JP, Barthelemy C, Mace B: Meiotic segregation of sex chromosomes in mosaic and non-mosaic XYY males: case reports and review of the literature. / Int J Androl 2003,26(4):242-49. CrossRef
    6. Park JH, Burns-Cusato M, Dominguez-Salazar E, Riggan A, Shetty S, Arnold AP, Rissman EF: Effects of sex chromosome aneuploidy on male sexual behavior. / Genes Brain Behav 2008,7(6):609-17. CrossRef
    7. Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L: A review of trisomy X (47, XXX). / Orphanet J Rare Dis 2010, 5:8. CrossRef
    8. Sybert VP, McCauley E: Turner’s syndrome. / N Engl J Med 2004,351(12):1227-238. CrossRef
    9. Mujezinovic F, Alfirevic Z: Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review. / Obstet Gynecol 2007,110(3):687-94. CrossRef
    10. Pitukkijronnakorn S, Promsonthi P, Panburana P, Udomsubpayakul U, Chittacharoen A: Fetal loss associated with second trimester amniocentesis. / Arch Gynecol Obstet 2011,284(4):793-97. CrossRef
    11. Kagan KO, Wright D, Valencia C, Maiz N, Nicolaides KH: Screening for trisomies 21, 18 and 13 by maternal age, fetal nuchal translucency, fetal heart rate, free beta-hCG and pregnancy-associated plasma protein-A. / Hum Reprod 2008,23(9):1968-975. CrossRef
    12. Canick J: Prenatal screening for trisomy 21: recent advances and guidelines. / Clin Chem Lab Med 2011,50(6):1003-008.
    13. Lo YM, Corbetta N, Chamberlain PF, Rai V, Sargent IL, Redman CW, Wainscoat JS: Presence of fetal DNA in maternal plasma and serum. / Lancet 1997,350(9076):485-87. CrossRef
    14. Simpson JL: Choosing the best prenatal screening protocol. / N Engl J Med 2005,353(19):2068-070. CrossRef
    15. Bischoff FZ, Sinacori MK, Dang DD, Marquez-Do D, Horne C, Lewis DE, Simpson JL: Cell-free fetal DNA and intact fetal cells in maternal blood circulation: implications for first and second trimester non-invasive prenatal diagnosis. / Hum Reprod Update 2002,8(6):493-00. CrossRef
    16. Illanes S, Denbow M, Kailasam C, Finning K, Soothill PW: Early detection of cell-free fetal DNA in maternal plasma. / Early Hum Dev 2007,83(9):563-66. CrossRef
    17. Lo YM, Zhang J, Leung TN, Lau TK, Chang AM, Hjelm NM: Rapid clearance of fetal DNA from maternal plasma. / Am J Hum Genet 1999,64(1):218-24. CrossRef
    18. Birch L, English CA, O’Donoghue K, Barigye O, Fisk NM, Keer JT: Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41?weeks of gestation. / Clin Chem 2005,51(2):312-20. CrossRef
    19. Lo YM, Tein MS, Lau TK, Haines CJ, Leung TN, Poon PM, Wainscoat JS, Johnson PJ, Chang AM, Hjelm NM: Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. / Am J Hum Genet 1998,62(4):768-75. CrossRef
    20. Lo YM, Tsui NB, Chiu RW, Lau TK, Leung TN, Heung MM, Gerovassili A, Jin Y, Nicolaides KH, Cantor CR, / et al.: Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection. / Nat Med 2007,13(2):218-23. CrossRef
    21. Tsui NB, Chiu RW, Ding C, El-Sheikhah A, Leung TN, Lau TK, Nicolaides KH, Lo YM: Detection of trisomy 21 by quantitative mass spectrometric analysis of single-nucleotide polymorphisms. / Clin Chem 2005,51(12):2358-362. CrossRef
    22. Tong YK, Ding C, Chiu RW, Gerovassili A, Chim SS, Leung TY, Leung TN, Lau TK, Nicolaides KH, Lo YM: Noninvasive prenatal detection of fetal trisomy 18 by epigenetic allelic ratio analysis in maternal plasma: theoretical and empirical considerations. / Clin Chem 2006,52(12):2194-202. CrossRef
    23. Chiu RW, Chan KC, Gao Y, Lau VY, Zheng W, Leung TY, Foo CH, Xie B, Tsui NB, Lun FM, / et al.: Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma. / Proc Natl Acad Sci USA 2008,105(51):20458-0463. CrossRef
    24. Fan HC, Blumenfeld YJ, Chitkara U, Hudgins L, Quake SR: Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood. / Proc Natl Acad Sci USA 2008,105(42):16266-6271. CrossRef
    25. Ehrich M, Deciu C, Zwiefelhofer T, Tynan JA, Cagasan L, Tim R, Lu V, McCullough R, McCarthy E, Nygren AO, / et al.: Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. / Am J Obstet Gynecol 2011,204(3):e201-e211. 205 CrossRef
    26. Chiu RW, Akolekar R, Zheng YW, Leung TY, Sun H, Chan KC, Lun FM, Go AT, Lau ET, To WW, / et al.: Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. / BMJ 2011, 342:c7401. CrossRef
    27. Chen EZ, Chiu RW, Sun H, Akolekar R, Chan KC, Leung TY, Jiang P, Zheng YW, Lun FM, Chan LY, / et al.: Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing. / PLoS One 2011,6(7):e21791. CrossRef
    28. Fan HC, Quake SR: Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics. / PLoS One 2010,5(5):e10439. CrossRef
    29. Lau TK, Chen F, Pan X, Pooh RK, Jiang F, Li Y, Jiang H, Li X, Chen S, Zhang X: Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing. / J Matern Fetal Neonatal Med 2011,25(8):1370-374. CrossRef
    30. Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Rayyan AA, Parzefall T, Lev D, Shalev S, Frydman M, / et al.: Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families. / Genome Biol 2011,12(9):R89. CrossRef
    31. Bell CJ, Dinwiddie DL, Miller NA, Hateley SL, Ganusova EE, Mudge J, Langley RJ, Zhang L, Lee CC, Schilkey FD, / et al.: Carrier testing for severe childhood recessive diseases by next-generation sequencing. / Sci Transl Med 2011,3(65):65ra64. CrossRef
    32. Cheung MS, Down TA, Latorre I, Ahringer J: Systematic bias in high-throughput sequencing data and its correction by BEADS. / Nucleic Acids Res 2011,39(15):e103. CrossRef
    33. Aird D, Ross MG, Chen WS, Danielsson M, Fennell T, Russ C, Jaffe DB, Nusbaum C, Gnirke A: Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries. / Genome Biol 2011,12(2):R18. CrossRef
    34. Liao GJ, Lun FM, Zheng YW, Chan KC, Leung TY, Lau TK, Chiu RW, Lo YM: Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles. / Clin Chem 2011,57(1):92-01. CrossRef
    35. Purwosunu Y, Sekizawa A, Okai T: Detection and quantification of fetal DNA in maternal plasma by using LightCycler technology. / Methods Mol Biol 2008, 444:231-38. CrossRef
    36. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1755-8794/5/57/prepub
  • 作者单位:Fuman Jiang (1)
    Jinghui Ren (2)
    Fang Chen (1)
    Yuqiu Zhou (3)
    Jiansheng Xie (4)
    Shan Dan (5)
    Yue Su (5)
    Jianhong Xie (3)
    Baomin Yin (3)
    Wen Su (3)
    Huakun Zhang (4)
    Wei Wang (1)
    Xianghua Chai (1)
    Linhua Lin (2)
    Hui Guo (2)
    Qiyun Li (2)
    Peipei Li (1)
    Yuying Yuan (1)
    Xiaoyu Pan (1)
    Yihan Li (1)
    Lifu Liu (1)
    Huifei Chen (1)
    Zhaoling Xuan (1)
    Shengpei Chen (1)
    Chunlei Zhang (1)
    Hongyun Zhang (1)
    Zhongming Tian (1)
    Zhengyu Zhang (1)
    Hui Jiang (1)
    Lijian Zhao (1)
    Weimou Zheng (1)
    Songgang Li (1)
    Yingrui Li (1)
    Jun Wang (1)
    Jian Wang (1)
    Xiuqing Zhang (1)

    1. BGI- Shenzhen, Shenzhen, China
    2. The Center of Prenatal Diagnosis, Shenzhen People’s Hospital, 2nd Clinical Medical College of Jinan University, Shenzhen, Guangdong, China
    3. Zhuhai Institute of Medical Genetics, Zhuhai Municipal Maternal and Child Healthcare Hospital, Zhuhai, China
    4. Central for Prenatal Diagnosis, Shenzhen Maternity and Child Healthcare Hospital, Affiliated Southern Medical University, Shenzhen, China
    5. Department of Perinatology, Beijing Obstetrics and Gynecology Hospital, Capital University of Medical Sciences, Beijing, China
  • ISSN:1755-8794
文摘
Background Conventional prenatal screening tests, such as maternal serum tests and ultrasound scan, have limited resolution and accuracy. Methods We developed an advanced noninvasive prenatal diagnosis method based on massively parallel sequencing. The Noninvasive Fetal Trisomy (NIFTY) test, combines an optimized Student’s t-test with a locally weighted polynomial regression and binary hypotheses. We applied the NIFTY test to 903 pregnancies and compared the diagnostic results with those of full karyotyping. Results 16 of 16 trisomy 21, 12 of 12 trisomy 18, two of two trisomy 13, three of four 45, X, one of one XYY and two of two XXY abnormalities were correctly identified. But one false positive case of trisomy 18 and one false negative case of 45, X were observed. The test performed with 100% sensitivity and 99.9% specificity for autosomal aneuploidies and 85.7% sensitivity and 99.9% specificity for sex chromosomal aneuploidies. Compared with three previously reported z-score approaches with/without GC-bias removal and with internal control, the NIFTY test was more accurate and robust for the detection of both autosomal and sex chromosomal aneuploidies in fetuses. Conclusion Our study demonstrates a powerful and reliable methodology for noninvasive prenatal diagnosis.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700