The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia

Pre-eclampsia is a lead ing cause of maternal and fetal mortality and morbidity. Early-onset pre-eclampsia occurring before 32 weeks gestation affects ~1% of pregnancies. At these gestations conservative management focussing on control of hypertension and seizure prevention, to gain fetal maturity i...

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Main Author: Everett, Thomas Richard
Published: University of Bristol 2015
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680140
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spelling ndltd-bl.uk-oai-ethos.bl.uk-6801402016-08-04T04:05:14ZThe effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsiaEverett, Thomas Richard2015Pre-eclampsia is a lead ing cause of maternal and fetal mortality and morbidity. Early-onset pre-eclampsia occurring before 32 weeks gestation affects ~1% of pregnancies. At these gestations conservative management focussing on control of hypertension and seizure prevention, to gain fetal maturity is key. Impaired nitric oxide bioavailability, is thought to play a major role in the maternal manifestations of pre-eclampsia such as hypertension and likewise platelet activation, proteinuria and oedema. There is no current treatment that targets the underlying pathophysiology. Uterine artery Doppler and arterial stiffness were assessed in ninety-nine women, at high a priori risk of pre-eclampsia. The study showed a positive correlation between increased uterine artery impedance and both pulse wave reflection (AI)() and aortic pulse wave velocity (aPWV). Alx was negatively correlated with neonatal birth weight. Infusion studies of S-nitrosoglutathione (GSNO) and labetalol, the standard antihypertensive used in pre-eclampsia, were performed in 12 healthy nonpregnant volunteers to assess the effects on Alx and aPWV and cardiac output. The study showed that GSNO and labetalol have similar effect on blood pressure, however GSI\lO, but not labetalol, reduces Alx. The primary outcome of the GSNO infusion study in preeclampsia was to establish the dose of GSNO at which there was optimal reduction in Alx, without causing a clinically significant fall in blood pressure. Secondary outcomes included the effect on platelet function, soluble biomarkers and proteinuria in the mother and Doppler parameters in both the mother and fetus. Six women underwent infusion and an infusion rate of 1O-30mcg/min GSNO was established as an optimal dose. GSNO significantly reduced platelet activation and trend towards reduction in proteinuria and soluble endoglin was seen. The effects of GSNO in women with preeclampsia and make GSNO a promising candidate for further investigation for the treatment of pre-eclampsia, either as a sole agent or adjunct to current treatments.618.3University of Bristolhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680140Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 618.3
spellingShingle 618.3
Everett, Thomas Richard
The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
description Pre-eclampsia is a lead ing cause of maternal and fetal mortality and morbidity. Early-onset pre-eclampsia occurring before 32 weeks gestation affects ~1% of pregnancies. At these gestations conservative management focussing on control of hypertension and seizure prevention, to gain fetal maturity is key. Impaired nitric oxide bioavailability, is thought to play a major role in the maternal manifestations of pre-eclampsia such as hypertension and likewise platelet activation, proteinuria and oedema. There is no current treatment that targets the underlying pathophysiology. Uterine artery Doppler and arterial stiffness were assessed in ninety-nine women, at high a priori risk of pre-eclampsia. The study showed a positive correlation between increased uterine artery impedance and both pulse wave reflection (AI)() and aortic pulse wave velocity (aPWV). Alx was negatively correlated with neonatal birth weight. Infusion studies of S-nitrosoglutathione (GSNO) and labetalol, the standard antihypertensive used in pre-eclampsia, were performed in 12 healthy nonpregnant volunteers to assess the effects on Alx and aPWV and cardiac output. The study showed that GSNO and labetalol have similar effect on blood pressure, however GSI\lO, but not labetalol, reduces Alx. The primary outcome of the GSNO infusion study in preeclampsia was to establish the dose of GSNO at which there was optimal reduction in Alx, without causing a clinically significant fall in blood pressure. Secondary outcomes included the effect on platelet function, soluble biomarkers and proteinuria in the mother and Doppler parameters in both the mother and fetus. Six women underwent infusion and an infusion rate of 1O-30mcg/min GSNO was established as an optimal dose. GSNO significantly reduced platelet activation and trend towards reduction in proteinuria and soluble endoglin was seen. The effects of GSNO in women with preeclampsia and make GSNO a promising candidate for further investigation for the treatment of pre-eclampsia, either as a sole agent or adjunct to current treatments.
author Everett, Thomas Richard
author_facet Everett, Thomas Richard
author_sort Everett, Thomas Richard
title The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
title_short The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
title_full The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
title_fullStr The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
title_full_unstemmed The effects of S-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
title_sort effects of s-nitrosoglutathione on vascular stiffness and platelet function in early-onset pre-eclampsia
publisher University of Bristol
publishDate 2015
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680140
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