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Markers of endothelial activation in preeclampsia
M Prochazka, J Prochazkova, M Lubusky, R Pilka, J Ulehlova, I Michalec, P Polak, M Kacerovsky, L Slavik
Jazyk angličtina Země Německo
Grantová podpora
NT14394
MZ0
CEP - Centrální evidence projektů
PubMed
25807636
Knihovny.cz E-zdroje
- MeSH
- biologické markery * krev MeSH
- CD antigeny krev MeSH
- cévní endotel patofyziologie MeSH
- dospělí MeSH
- endoteliální receptor proteinu C MeSH
- inhibitor aktivátoru plazminogenu 1 krev MeSH
- lidé MeSH
- mladý dospělý MeSH
- preeklampsie * krev patofyziologie MeSH
- prospektivní studie MeSH
- první trimestr těhotenství * krev MeSH
- receptory buněčného povrchu krev MeSH
- referenční hodnoty MeSH
- studie případů a kontrol MeSH
- těhotenství MeSH
- tkáňový aktivátor plazminogenu krev MeSH
- trombomodulin krev MeSH
- von Willebrandův faktor metabolismus MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
BACKGROUND: The study aimed at finding a laboratory approach to detect endothelial damage in normal pregnancy as well as in pregnancy complicated by preeclampsia using selected markers of endothelial activation. MATERIALS: A total of 403 healthy pregnant women without a history of deep vein thrombosis and/or hypertension were prospectively studied. From all women, venous blood was collected before the end of the 1st trimester, between weeks 24 and 28 of gestation, and in the 3rd trimester (weeks 34-36). Assays of tissue plasminogen activator, plasminogen activator inhibitor-1, von Willebrand factor activity and antigen, thrombomodulin, endothelial protein C receptor, and endothelial microparticles activated by TF were performed. RESULTS: When comparing women who developed preeclampsia during pregnancy (the average levels were 23.41 mug/L, 34.33 mug/L, and 53.56 mug/L in the 1st, 2nd, and 3rd trimesters, respectively) with healthy pregnant women (the average levels were 19.05 mug/L, 28.47 mug/L, and 39.86 mug/L in the 1st, 2nd, and 3rd trimesters, respectively) significant differences in the levels of thrombomodulin were found in all three trimesters. By contrast, no statistically significant differences in the levels of vWF (both antigen and activity), t-PA, EPCR, EMPs, MMP-2, MMP-9, and TIMP-9 were found in any trimesters in the same group. CONCLUSIONS: Pregnancy and preeclampsia strongly influence the levels of studied markers. The findings of this work confirm the possible predictive potential of thrombomodulin and PA-1.
Department of Hemato Oncology University Hospital Ostrava Czech Republic
Department of Obsterics and Gynecology Charles University Hradec Králové Czech Republic
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- $a BACKGROUND: The study aimed at finding a laboratory approach to detect endothelial damage in normal pregnancy as well as in pregnancy complicated by preeclampsia using selected markers of endothelial activation. MATERIALS: A total of 403 healthy pregnant women without a history of deep vein thrombosis and/or hypertension were prospectively studied. From all women, venous blood was collected before the end of the 1st trimester, between weeks 24 and 28 of gestation, and in the 3rd trimester (weeks 34-36). Assays of tissue plasminogen activator, plasminogen activator inhibitor-1, von Willebrand factor activity and antigen, thrombomodulin, endothelial protein C receptor, and endothelial microparticles activated by TF were performed. RESULTS: When comparing women who developed preeclampsia during pregnancy (the average levels were 23.41 mug/L, 34.33 mug/L, and 53.56 mug/L in the 1st, 2nd, and 3rd trimesters, respectively) with healthy pregnant women (the average levels were 19.05 mug/L, 28.47 mug/L, and 39.86 mug/L in the 1st, 2nd, and 3rd trimesters, respectively) significant differences in the levels of thrombomodulin were found in all three trimesters. By contrast, no statistically significant differences in the levels of vWF (both antigen and activity), t-PA, EPCR, EMPs, MMP-2, MMP-9, and TIMP-9 were found in any trimesters in the same group. CONCLUSIONS: Pregnancy and preeclampsia strongly influence the levels of studied markers. The findings of this work confirm the possible predictive potential of thrombomodulin and PA-1.
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