The search for thrombophilic gene mutations in women with gestational hypertension does not help in predicting poor pregnancy outcome

被引:13
作者
D'Aniello, G
Florio, P
Sabatini, L
Severi, FM
Fineschi, D
Cito, G
Guidoni, CG
Petraglia, F
机构
[1] Univ Siena, Policlin Le Scotte, Dept Pediat Obstet & Reprod, Chair Obstet & Gynecol, I-53100 Siena, Italy
[2] Azienda Osped Senese, UO Lab Ematol & Coagulaz, Siena, Italy
关键词
Factor V Leiden; PAI-1; polymorphism; prothrombin; methylenetetrahydrofolate reductase; Doppler; factor II : C; uterine arteries;
D O I
10.1097/00004872-200310000-00019
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective To evaluate whether genetic thrombophilic mutations, biochemical and biophysical indices help to predict pregnancy outcome in women with gestational hypertension. Design and methods A group of 59 women with gestational hypertension were prospectively tested between 24 and 26 weeks of gestation for: (i) DNA analysis to search for gene mutations of Factor V Leiden, prothrombin, methylenetetrahydrofolate reductase and plasminogen activator inhibitor type 1 (PAI-1) polymorphism; (ii) maternal serum concentrations of homocysteine and PAI-1, activated protein resistance and Factor II:C activity levels; (iii) mean uterine arterial resistance index (RI) by Doppler velocimetry; and (iv) history of hypertensive disorders in relatives (the mother and/or the father). Pregnancy outcome was evaluated, and considered 'poor' when patients developed severe pre-eclampsia, haemolysis-elevated liver enzymes-low platelets (HELLP) syndrome, fetal growth restriction (FGR), thromboembolic complications and disseminated intravascular coagulopathy (DIC). Results Eighteen women had a poor pregnancy outcome (11 with severe pre-eclampsia, of whom two had superimposed FGR; three with full HELLP syndrome, of whom one had DIC; four with FGR) and delivered, by emergency Caesarean section, neonates with a significantly lower mean gestational age (P < 0.0001) and birthweight (P < 0.0001). History of hypertensive disorders was significantly (P < 0.001) more common in the women group with poor (111 of 18) than normal (110 of 41) outcome. In addition, patients with a poor pregnancy outcome did not have a higher incidence of gene polymorphisms incidence, but significantly (P < 0.01) higher Factor II:C activity levels and significantly (P < 0.0001) higher mean uterine arterial RI than women with normal pregnancy outcome. Conclusions Only Factor II:C activity levels, uterine arterial Doppler and a hystory of familial hypertension are useful in predicting poor pregnancy outcome in gestational hypertension. (C) 2003 Lippincott Williams Wilkins.
引用
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页码:1915 / 1920
页数:6
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