The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy

Objective: To determine the relationship between a priori risk for fetal trisomy and the fraction of fetal cell-free DNA (cfDNA) in maternal blood. Methods: A comparative analysis on fetal cfDNA amounts was performed in subjects stratified into a priori risk groups based on maternal age, prenatal sc...

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Published inThe journal of maternal-fetal & neonatal medicine Vol. 26; no. 2; pp. 143 - 145
Main Authors Brar, Herb, Wang, Eric, Struble, Craig, Musci, Thomas J., Norton, Mary E.
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 01.01.2013
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Abstract Objective: To determine the relationship between a priori risk for fetal trisomy and the fraction of fetal cell-free DNA (cfDNA) in maternal blood. Methods: A comparative analysis on fetal cfDNA amounts was performed in subjects stratified into a priori risk groups based on maternal age, prenatal screening results, or nuchal translucency measurement. Results: Across the highest and lowest deciles within each group, there were no significant differences in the fetal cfDNA fraction. Conclusions: These data support the concept that non-invasive prenatal test performance as determined by fetal cfDNA fraction is not predicted to be different based on patient risk classification.
AbstractList Objective: To determine the relationship between a priori risk for fetal trisomy and the fraction of fetal cell-free DNA (cfDNA) in maternal blood. Methods: A comparative analysis on fetal cfDNA amounts was performed in subjects stratified into a priori risk groups based on maternal age, prenatal screening results, or nuchal translucency measurement. Results: Across the highest and lowest deciles within each group, there were no significant differences in the fetal cfDNA fraction. Conclusions: These data support the concept that non-invasive prenatal test performance as determined by fetal cfDNA fraction is not predicted to be different based on patient risk classification.
To determine the relationship between a priori risk for fetal trisomy and the fraction of fetal cell-free DNA (cfDNA) in maternal blood. A comparative analysis on fetal cfDNA amounts was performed in subjects stratified into a priori risk groups based on maternal age, prenatal screening results, or nuchal translucency measurement. Across the highest and lowest deciles within each group, there were no significant differences in the fetal cfDNA fraction. These data support the concept that non-invasive prenatal test performance as determined by fetal cfDNA fraction is not predicted to be different based on patient risk classification.
Author Wang, Eric
Brar, Herb
Norton, Mary E.
Struble, Craig
Musci, Thomas J.
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  surname: Brar
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  givenname: Eric
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  organization: Ariosa Diagnostics
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  organization: Ariosa Diagnostics
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  givenname: Mary E.
  surname: Norton
  fullname: Norton, Mary E.
  organization: Stanford University/Lucile Packard Children's Hospital
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Snippet Objective: To determine the relationship between a priori risk for fetal trisomy and the fraction of fetal cell-free DNA (cfDNA) in maternal blood. Methods: A...
To determine the relationship between a priori risk for fetal trisomy and the fraction of fetal cell-free DNA (cfDNA) in maternal blood. A comparative analysis...
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StartPage 143
SubjectTerms Adolescent
Adult
cell-free DNA
DNA - blood
Female
Humans
Maternal Age
Middle Aged
Non-invasive
Nuchal Translucency Measurement
Pregnancy
prenatal diagnosis
Risk Factors
Trisomy - diagnosis
trisomy risk
Young Adult
Title The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy
URI https://www.tandfonline.com/doi/abs/10.3109/14767058.2012.722731
https://www.ncbi.nlm.nih.gov/pubmed/22913322
Volume 26
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