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Soluble endoglin and transforming growth factor-beta1 in women who subsequently developed preeclampsia.

Authors :
Lim JH
Kim SY
Park SY
Lee MH
Yang JH
Kim MY
Chung JH
Lee SW
Ryu HM
Lim, Ji Hyae
Kim, Shin Young
Park, So Yeon
Lee, Moon Hee
Yang, Jae Hyug
Kim, Moon Young
Chung, Jin Hoon
Lee, Si Won
Ryu, Hyun Mee
Source :
Prenatal Diagnosis; May2009, Vol. 29 Issue 5, p471-476, 6p
Publication Year :
2009

Abstract

<bold>Objective: </bold>This study aimed to analyze the differences of soluble endoglin (sEng) and transforming growth factor-beta1 (TGF-beta1) according to preeclamptic complications and to investigate the correlation between these factors and the clinical symptoms of preeclampsia. <bold>Method: </bold>We estimated the levels of sEng and TGF-beta1 in plasma collected in the second trimester at the time of genetic amniocentesis from 60 women who subsequently developed preeclampsia and 124 contemporaneous normotensive women. <bold>Results: </bold>sEng levels were higher in cases than in controls, whereas TGF-beta1 levels were lower (P < 0.001). sEng levels, but not TGF-beta1 levels, were higher in cases with severe or preterm delivery than in cases with mild preeclampsia or term delivery (P < 0.001) and were increased in cases destined to deliver a small gestational age neonate (P < 0.001). Moreover, sEng levels, but not TGF-beta1 levels, showed a positive correlation with maximum diastolic and systolic blood pressure (r = 0.57, P < 0.001; and r = 0.33, P < 0.001, respectively) and proteinuria (r = 0.42, P < 0.001). <bold>Conclusion: </bold>Early midtrimester plasma levels of sEng are predictive of subsequence occurrence and severity of preeclampsia, in terms of severity of hypertension and proteinuria, prematurity, and association with small for gestational age neonates. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01973851
Volume :
29
Issue :
5
Database :
Complementary Index
Journal :
Prenatal Diagnosis
Publication Type :
Academic Journal
Accession number :
105515199
Full Text :
https://doi.org/10.1002/pd.2217