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Obesity and no call results: optimal timing of cell-free DNA testing and redraw.
Hopkins, Maeve K; Koelper, Nathanael; Caldwell, Samantha; Dyr, Brittany; Dugoff, Lorraine.
Afiliação
  • Hopkins MK; Division of Maternal-Fetal Medicine, Women's Health Institute, Cleveland Clinic, Cleveland, OH. Electronic address: hopkinm7@ccf.org.
  • Koelper N; Department of Obstetrics and Gynecology, Center for Research on Reproduction and Women's Health, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Caldwell S; Laboratory Corporation of America Holdings, Sequenom Center for Molecular Medicine, LLC, San Diego, CA.
  • Dyr B; Laboratory Corporation of America Holdings, Sequenom Center for Molecular Medicine, LLC, San Diego, CA.
  • Dugoff L; Divisions of Reproductive Genetics and Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Am J Obstet Gynecol ; 225(4): 417.e1-417.e10, 2021 10.
Article em En | MEDLINE | ID: mdl-33839096
ABSTRACT

BACKGROUND:

Fetal fraction of cell-free DNA decreases with increasing maternal weight. Consequently, cell-free DNA screening for fetal aneuploidy has higher screen failures or "no call" rates in women with obesity owing to a low fetal fraction. The optimal timing of testing based on maternal weight is unknown.

OBJECTIVE:

This study aimed to identify the optimal timing of initial cell-free DNA testing based on maternal weight and to identify the optimal timing of repeat cell-free DNA testing in cases with an initial screen failure. STUDY

DESIGN:

This was a retrospective cohort study of women undergoing cell-free DNA for fetal aneuploidy screening between 9 and 18 weeks through a single laboratory over 1 year from 2018 to 2019. Fetal fraction change per week was calculated, and generalized linear models were used to calculate relative risk and 95% confidence interval of a no call result at given maternal weights and gestational ages.

RESULTS:

The vast majority of samples (99.22%) received a test result. The risk of a no call result owing to a low fetal fraction was higher with increasing maternal weight. At 9 to 12 weeks, the rate of a no call result owing to a low fetal fraction in women who weighed <150 lb was 0.14% compared with 17.39% in women weighing >400 lb. Fetal fraction increased with increasing gestational age, although the incremental increase in fetal fraction over time is inversely proportional to maternal weight. At 13 to 18 weeks' gestation, 6.45% of women weighing >400 lb received a no call result owing to a low fetal fraction. In women in the highest weight category, >400 lb, fetal fraction increased 0.5% with each week of gestation.

CONCLUSION:

Although the risk of a no call result increases with maternal weight, cell-free DNA screening should be offered to all women at 9 to 12 weeks' gestation, allowing the option to have chorionic villus sampling after a positive test result. Pretest counseling for women with obesity should include the increased chance for a test failure. Most women weighing less than 400 lb will receive a test result and more than 80% of women with a weight of >400 lb will receive a test result at 9 to 12 weeks' gestation. Data regarding the expected increase in cell-free DNA fetal fraction per week may help guide the timing of a redraw to optimize test success.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Idade Gestacional / Transtornos Cromossômicos / Ácidos Nucleicos Livres / Teste Pré-Natal não Invasivo / Obesidade Materna Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Idade Gestacional / Transtornos Cromossômicos / Ácidos Nucleicos Livres / Teste Pré-Natal não Invasivo / Obesidade Materna Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article