Soluble fms-Like Tyrosine Kinase 1 (sFlt1), Endoglin and Placental Growth Factor (PlGF) in Preeclampsia among High Risk Pregnancies

被引:125
作者
Powers, Robert W. [1 ]
Jeyabalan, Arun [1 ]
Clifton, Rebecca G. [2 ]
Van Dorsten, Peter [3 ]
Hauth, John C. [4 ]
Klebanoff, Mark A. [5 ]
Lindheimer, Marshall D. [6 ]
Sibai, Baha [7 ]
Landon, Mark [8 ]
Miodovnik, Menachem [9 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Obstet Gynecol & Womens Hlth, Pittsburgh, PA 15260 USA
[2] George Washington Univ, Ctr Biostat, Washington, DC USA
[3] Med Univ S Carolina, Dept Obstet & Gynecol, Charleston, SC 29425 USA
[4] Univ Alabama Birmingham, Sch Med, Dept Obstet & Gynecol, Birmingham, AL USA
[5] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Bethesda, MD USA
[6] Univ Chicago, Sch Med, Dept Obstet & Gynecol, Chicago, IL 60637 USA
[7] Univ Tennessee, Dept Obstet & Gynecol, Sch Med, Memphis, TN 38103 USA
[8] Ohio State Univ, Sch Med, Dept Obstet & Gynecol, Columbus, OH 43210 USA
[9] Univ Cincinnati, Sch Med, Dept Obstet & Gynecol, Cincinnati, OH USA
关键词
ANTIANGIOGENIC FACTORS; PREVENTION; WOMEN;
D O I
10.1371/journal.pone.0013263
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Differences in circulating concentrations of antiangiogenic factors sFlt1 and soluble endoglin (sEng) and the pro-angiogenic growth factor PlGF are reported to precede the onset of preeclampsia weeks to months in low-risk pregnant women. The objective of this study was to investigate whether similar changes can be detected in pregnant women at high-risk to develop the syndrome. Methods: This study is a secondary analysis of the NICHD MFMU trial of aspirin to prevent preeclampsia in high-risk pregnancies. Serum samples were available from 194 women with pre-existing diabetes, 313 with chronic hypertension, 234 with multifetal gestation, and 252 with a history of preeclampsia in a previous pregnancy. Samples collected across pregnancy were analyzed in a blinded fashion for sFlt1, sEng and PlGF. Results: The odds of developing preeclampsia were significantly increased among women with multiple fetuses for each 2-fold elevation in sFlt1, sEng and the ratio of angiogenic factors (e.g. OR 2.18, 95% CI 1.46-3.32), and significantly decreased for each 2-fold elevation in circulating PlGF (OR 0.50, 95% CI 0.30-0.82) between 7 and 26 weeks' gestation. Cross-sectional analysis of the angiogenic factors across gestation showed significant differences during the third trimester in women who develop preeclampsia compared with appropriate controls in all high-risk groups. However, when data were examined in relation to the gestational week when preeclampsia was diagnosed only sFlt1 was significantly higher 2 to 5 weeks before the clinical onset of preeclampsia and only in women with previous preeclampsia. Conclusions: The pattern of elevated concentrations of sFlt1 and sEng, and low PlGF in high-risk pregnant subjects who develop preeclampsia is similar to that reported in low-risk pregnant women. However, differences in these factors among high-risk women who do and do not develop preeclampsia are modest, and do not appear to be clinically useful predictors in these high-risk pregnant women.
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页数:12
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