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 in | The journal of maternal-fetal & neonatal medicine Vol. 26; no. 2; pp. 143 - 145 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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. |
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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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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22913322$$D View this record in MEDLINE/PubMed |
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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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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 |
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