Literature DB >> 25364649

Noninvasive prenatal testing in China: Future detection of rare genetic diseases?

Lin Mei1, Qi Tang2, Baiyu Sun3, Lingzhong Xu2.   

Abstract

Noninvasive prenatal testing (NIPT) provides an innovative method to detect genetic conditions in fetuses using a maternal blood sample, thus avoiding the risk of miscarriage associated with traditional invasive procedures. Since 80% of rare diseases are genetic diseases, NIPT has the potential to detect rare genetic diseases early on and it has been used in many countries and regions. Since China has the world's largest population of patients with rare diseases, NIPT has been implemented in China since 2010. However, the regulations governing NIPT in China are weak and NIPT oversight and research are still lacking. Strict registration is needed to ensure the quality of NIPT, additional certification can help a developer/manufacturer of an NIPT test to compile clinical data and to improve innovation, and academic societies can provide committee opinions that are suited to the current situation in China. These efforts may improve regulations governing NIPT and NIPT oversight and research in China. With these improvements, NIPT may offer promise in terms of the early detection of rare diseases.

Entities:  

Keywords:  Clinical Laboratory Improvement Amendments (CLIA); Committee opinion; Laboratory Developed Tests (LDTs); Premarket notification

Year:  2014        PMID: 25364649      PMCID: PMC4214242          DOI: 10.5582/irdr.2014.01012

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  10 in total

1.  Presence of fetal DNA in maternal plasma and serum.

Authors:  Y M Lo; N Corbetta; P F Chamberlain; V Rai; I L Sargent; C W Redman; J S Wainscoat
Journal:  Lancet       Date:  1997-08-16       Impact factor: 79.321

2.  Revisiting oversight and regulation of molecular-based laboratory-developed tests: a position statement of the Association for Molecular Pathology.

Authors:  Andrea Ferreira-Gonzalez; Rajyasree Emmadi; Stephen P Day; Robert F Klees; Jennifer R Leib; Elaine Lyon; Jan A Nowak; Victoria M Pratt; Mary S Williams; Roger D Klein
Journal:  J Mol Diagn       Date:  2014-01       Impact factor: 5.568

3.  Rare diseases and legislation in China.

Authors:  Jing-Bo Wang; Jeff J Guo; Li Yang; Yan-De Zhang; Zhao-Qi Sun; Yan-Jun Zhang
Journal:  Lancet       Date:  2010-02-27       Impact factor: 79.321

4.  The predictive capacity of personal genome sequencing.

Authors:  Nicholas J Roberts; Joshua T Vogelstein; Giovanni Parmigiani; Kenneth W Kinzler; Bert Vogelstein; Victor E Velculescu
Journal:  Sci Transl Med       Date:  2012-04-02       Impact factor: 17.956

Review 5.  Current situation and prospects of newborn screening and treatment for Phenylketonuria in China - compared with the current situation in the United States, UK and Japan.

Authors:  Lin Mei; Peipei Song; Norihiro Kokudo; Lingzhong Xu; Wei Tang
Journal:  Intractable Rare Dis Res       Date:  2013-11

6.  Research into rare diseases of childhood.

Authors:  Mark L Batshaw; Stephen C Groft; Jeffrey P Krischer
Journal:  JAMA       Date:  2014-05-07       Impact factor: 56.272

7.  Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.

Authors:  Patricia L Devers; Amy Cronister; Kelly E Ormond; Flavia Facio; Campbell K Brasington; Pamela Flodman
Journal:  J Genet Couns       Date:  2013-01-22       Impact factor: 2.537

8.  Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.

Authors:  Siân Jones; Ralph H Hruban; Mihoko Kamiyama; Michael Borges; Xiaosong Zhang; D Williams Parsons; Jimmy Cheng-Ho Lin; Emily Palmisano; Kieran Brune; Elizabeth M Jaffee; Christine A Iacobuzio-Donahue; Anirban Maitra; Giovanni Parmigiani; Scott E Kern; Victor E Velculescu; Kenneth W Kinzler; Bert Vogelstein; James R Eshleman; Michael Goggins; Alison P Klein
Journal:  Science       Date:  2009-03-05       Impact factor: 47.728

Review 9.  Non-invasive prenatal diagnosis: progress and potential.

Authors:  Rebecca Daley; Melissa Hill; Lyn S Chitty
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2014-04-30       Impact factor: 5.747

10.  Exome sequencing identifies the cause of a mendelian disorder.

Authors:  Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure; Michael J Bamshad
Journal:  Nat Genet       Date:  2009-11-13       Impact factor: 38.330

  10 in total
  2 in total

1.  "The Top Priority Is a Healthy Baby": Narratives of Health, Disability, and Abortion in Online Pregnancy Forum Discussions in the US and China.

Authors:  Grace Li; Subhashini Chandrasekharan; Megan Allyse
Journal:  J Genet Couns       Date:  2016-06-09       Impact factor: 2.537

2.  Clinical evaluation of non-invasive prenatal screening in 32,394 pregnancies from Changzhi maternal and child health care hospital of Shanxi China.

Authors:  XiaoZe Li; LiHong Wang; ZeRong Yao; FangYing Ruan; ZhiPeng Hu; WenXia Song
Journal:  J Med Biochem       Date:  2022-07-29       Impact factor: 2.157

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.