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DOI 10.1002/pd.5260

Медицинская библиотека · Prenatal diagnosis · 2018

Biological explanations for discordant noninvasive prenatal test results: Preliminary data and lessons learned.

Wilkins-Haug Louise, Zhang Chengsheng, Cerveira Eliza, Ryan Mallory, Mil-Homens Adam, Zhu Qihui, Reddi Honey, Lee Charles, Bianchi Diana W

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

Maternal plasma cell-free DNA (cfDNA) analysis is a powerful screening tool for Down syndrome. In a pilot series, we examined biologic causes of discordance between the cfDNA test results and the fetal karyotype. We also explored the feasibility of obtaining trio biospecimens by using parental engagement.

METHODS

A convenience sample of women with discordant cfDNA results were recruited by their care providers. We provided shipping materials and instructions for biospecimen collection. Maternal, newborn, and placental samples were examined with droplet digital PCR.

RESULTS

Thirteen of 15 women successfully had biospecimens obtained remotely. High-quality DNA was extracted in 12 of 13 women. Presumed biologic etiologies for discordance were identified in 7 of 12 women: 3 cases from additional clinical review (male renal transplant, vanishing twin, and colon cancer) and 4 cases from additional laboratory investigation using droplet digital PCR (3 with confined placental mosaicism and 1 with true fetal mosaicism).

CONCLUSIONS

Understanding the biology behind cfDNA-fetal karyotype discordancy is useful for follow-up clinical care. Our study suggests that most cases could be resolved by using a trio biospecimen protocol and parental involvement. To improve accuracy, additional sequencing of biospecimens will be required.

Для цитирования: Wilkins-Haug Louise, Zhang Chengsheng, Cerveira Eliza, Ryan Mallory, Mil-Homens Adam, Zhu Qihui, Reddi Honey, Lee Charles, Bianchi Diana W. Biological explanations for discordant noninvasive prenatal test results: Preliminary data and lessons learned.. Prenatal diagnosis. 2018. DOI: 10.1002/pd.5260.

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