Am J Perinatol 2017; 34(02): 191-198
DOI: 10.1055/s-0035-1570383
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Cell-Free Total and Fetal DNA in First Trimester Maternal Serum and Subsequent Development of Preeclampsia

Robert M. Silver
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
2   Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah
,
Leslie Myatt
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
3   University of Cincinnati, Cincinnati, Ohio
,
John C. Hauth
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
4   University of Alabama at Birmingham, Birmingham, Alabama
,
Kenneth J. Leveno
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
5   University of Texas Southwestern Medical Center, Dallas, Texas
,
Alan M. Peaceman
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
6   Northwestern University, Chicago, Illinois
,
Susan M. Ramin
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
7   Children's Memorial Hermann Hospital, University of Texas Health Science Center at Houston, Houston, Texas
,
Philip Samuels
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
8   The Ohio State University, Columbus, Ohio
,
George Saade
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
9   University of Texas Medical Branch, Galveston, Texas
,
Yoram Sorokin
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
10   Wayne State University, Detroit, Michigan
,
Rebecca G. Clifton
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
11   Biostatistics Center, The George Washington University, Washington, District of Columbia
,
Uma M. Reddy
1   Eunice Kennedy Shriver National Institute of Child Health and Human Development, Maternal-Fetal Medicine Units Network, Bethesda, Maryland
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Publikationsverlauf

11. Juni 2015

06. November 2015

Publikationsdatum:
11. Juli 2016 (online)

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Abstract

Objective The objective of this study was to assess the relationship between first trimester cell-free total and fetal DNA in maternal plasma and the subsequent development of preeclampsia.

Study Design Nested case–control study of patients enrolled in the Combined Antioxidant and Preeclampsia Prediction Studies prediction study of 175 women who did and 175 women who did not develop preeclampsia. The predictive values of cell-free total and fetal DNA and the subsequent development of preeclampsia were measured using receiver operating characteristic curves.

Results Cell-free total DNA was higher in African American (median; 25–75%; 6.15; 0.14–28.73; p = 0.02) and Hispanic (4.95; 0.20–26.82; p = 0.037) compared with white women (2.33; 0.03–13.10). Levels of cell-free total DNA were also associated with maternal body mass index (BMI) (p = 0.02). Cell-free total DNA levels were similar between women who later developed preeclampsia (3.52; 0.11–25.3) and controls (3.74; 0.12–21.14, p = 0.96).

Conclusion There is no significant difference in levels of cell-free total DNA in the first trimester in women who subsequently develop preeclampsia. Levels of cell-free total DNA in the first trimester are increased in African American and Hispanic compared with white women, and levels increase with increasing BMI.