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Extending non-invasive prenatal testing to non-invasive prenatal diagnosis
  1. Rachel Helen Horton,
  2. Diana Gay Wellesley
  1. Wessex Clinical Genetics Service, G Level, Princess Anne Hospital, Southampton, UK
  1. Correspondence to Dr Rachel Helen Horton, Wessex Clinical Genetics Service, G level, Princess Anne Hospital, Southampton SO16 5YA, UK; Rachel.Horton{at}

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Molecular prenatal diagnosis of genetic conditions has historically required invasive procedures to obtain a sample of tissue from a developing pregnancy—either from the placenta (chorionic villus sampling) or from the amniotic fluid (amniocentesis). Both have a small risk of causing a miscarriage, and the earliest point at which testing can be undertaken is 11 weeks into a pregnancy (for CVS). Non-invasive prenatal testing (NIPT) is an exciting step forward in prenatal genetic diagnosis, whereby fetal DNA can be obtained and tested by taking blood samples from a pregnant mother. This avoids the miscarriage risk associated with invasive prenatal tests and can also be performed at an earlier stage of gestation. The paper by Duan et al 1 demonstrates the great potential benefits of this new technology for families affected by genetic conditions.

The presence of cell-free fetal DNA in maternal blood was demonstrated in 1997 by Lo et al, who showed that Y-chromosome-derived sequences were present in serum samples from women pregnant with male fetuses. This cell-free fetal DNA is derived from the placenta: it has placental epigenetic signatures and is present in anembryonic pregnancies. Cell-free fetal DNA fragments are shorter than background maternally derived free DNA fragments, and the concentration of fetal DNA in maternal serum rises as a pregnancy advances.2

NIPT: screening in pregnancy

NIPT exploits the presence of cell-free fetal DNA to allow genetic testing of fetal material without the need for an invasive procedure. From the first study that showed the potential to establish fetal sex by detecting Y-chromosome-derived sequences, later studies went on to …

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  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent Not required.

  • Provenance and peer review Commissioned; externally peer reviewed.

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