Recent Advances in the Noninvasive Prenatal Testing for Chromosomal Abnormalities Using Maternal Plasma DNA
Autor: | Tak Yeung Leung, Xiaofan Zhu, Tze Kin Lau, Yvonne K. Kwok, Kwong Wai Choy |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
medicine.medical_specialty 030219 obstetrics & reproductive medicine Screening test business.industry Obstetrics Plasma dna Reproductive medicine Diagnostic test 030105 genetics & heredity Predictive value 03 medical and health sciences 0302 clinical medicine Prenatal screening Chromosomal structural abnormalities Modeling and Simulation Medicine Detection rate business |
Zdroj: | Journal of Fetal Medicine. :17-23 |
ISSN: | 2348-8859 2348-1153 |
DOI: | 10.1007/s40556-019-00229-3 |
Popis: | Abstract No single invention in the past has created such a rapid and massive impact on clinical obstetric practice as the introduction of noninvasive prenatal screening (NIPS) for chromosomal abnormalities using cell-free DNA in maternal plasma. However, the technology of NIPS which has also been called noninvasive prenatal testing (NIPT) is rapidly evolving. Most clinicians may not be able to fully understand this new technology to enable good clinical practice. This review will be focused on issues that have important clinical implications. NIPT/S is only a screening test and all positive cases must be confirmed by invasive diagnostic techniques. Although NIPT/S is being expanded rapidly to cover other chromosomes and large chromosomal structural abnormalities, the detection rate is still uncertain, and the positive predictive value is expected to be lower. Pregnant women who are at risk of chromosomal abnormalities other than common trisomies should be offered a diagnostic test instead of NIPT/S. The use of NIPT/S as a primary Down syndrome screening test should not replace the 11–13 weeks scan. |
Databáze: | OpenAIRE |
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