Markers of maternal cardiac dysfunction in pre-eclampsia and superimposed pre-eclampsia.


Journal

European journal of obstetrics, gynecology, and reproductive biology
ISSN: 1872-7654
Titre abrégé: Eur J Obstet Gynecol Reprod Biol
Pays: Ireland
ID NLM: 0375672

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 27 02 2019
revised: 11 03 2019
accepted: 18 04 2019
pubmed: 6 5 2019
medline: 19 12 2019
entrez: 4 5 2019
Statut: ppublish

Résumé

Frances Conti-Ramsden MBBS Academic Clinical Fellow To determine whether glycogen phosphorylase isoenzyme B (GPBB) and/or brain natriuretic peptide (BNP) concentrations are elevated in pre-eclampsia and superimposed pre-eclampsia (SPE), demonstrating cardiac ischaemia and strain. A nested case-control study was performed using samples and clinical data available from a prospective pregnancy cohort. Four groups were selected: healthy pregnant controls (n = 21), pre-eclampsia (n = 19), pre-existing chronic hypertension (CHT) and/or chronic kidney disease (CKD) without (n = 20) or with superimposed pre-eclampsia (SPE) (n = 19). Plasma samples were taken at time of disease or the third trimester in controls. Plasma concentrations of GPBB and BNP. There was no significant difference in GPBB plasma concentrations between controls and pre-eclampsia (geometric mean (GM) [95% CI]: 4.74 [2.54-8.84]ng/mL vs 5.01 [2.58-9.74]ng/mL, p = 0.90)), or between CHT and/or CKD and SPE (GM [95% CI]: 9.49 [4.93-18.25]ng/mL vs 10.24 [5.27-19.92]ng/mL, p = 0.87). BNP plasma concentrations were significantly raised in women with pre-eclampsia compared to controls (GM [95% CI]: 31.83 [20.18-50.22]pg/mL vs 11.33 [7.34-17.51]pg/mL, p = 0.001). Women with CKD, but not CHT, who developed SPE had elevated BNP concentrations. There were no significant differences in BNP concentration between women with comorbidity (CHT and/or CKD) and controls. GPBB has a limited role as a biomarker in hypertensive disorders of pregnancy. BNP concentrations were elevated in pre-eclampsia compared to controls. This suggests cardiac strain at the time of pre-eclampsia. Further studies are needed to examine whether BNP can identify women at increased risk of cardiovascular disease.

Identifiants

pubmed: 31051418
pii: S0301-2115(19)30198-8
doi: 10.1016/j.ejogrb.2019.04.034
pii:
doi:

Substances chimiques

Biomarkers 0
Natriuretic Peptide, Brain 114471-18-0
Glycogen Phosphorylase EC 2.4.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

151-156

Subventions

Organisme : Department of Health
ID : EME/15/23/02
Pays : United Kingdom
Organisme : Department of Health
ID : RP-2014-05-019
Pays : United Kingdom

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Frances Conti-Ramsden (F)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK. Electronic address: fran.conti-ramsden@kcl.ac.uk.

Carolyn Gill (C)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK. Electronic address: carolyn.gill@kcl.ac.uk.

Paul T Seed (PT)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK. Electronic address: paul.seed@kcl.ac.uk.

Kate Bramham (K)

Department of Renal Medicine, Division of Transplantation Immunology and Mucosal Biology, King's College London, London, UK. Electronic address: kate.bramham@kcl.ac.uk.

Lucy C Chappell (LC)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK. Electronic address: lucy.chappell@kcl.ac.uk.

Fergus P McCarthy (FP)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK; The Irish Centre for Fetal and Neonatal Translational Research, University College Cork, Wilton, Ireland Cork, Ireland. Electronic address: fergus.mccarthy@ucc.ie.

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Classifications MeSH