Intrauterine growth restriction, soluble fms-like tyrosine kinase-1 to placental growth factor ratio increase and preeclampsia.


Journal

Journal of gynecology obstetrics and human reproduction
ISSN: 2468-7847
Titre abrégé: J Gynecol Obstet Hum Reprod
Pays: France
ID NLM: 101701588

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 28 11 2018
accepted: 07 05 2019
pubmed: 16 5 2019
medline: 1 4 2020
entrez: 16 5 2019
Statut: ppublish

Résumé

Intrauterine growth restriction (IUGR) and preeclampsia (PE) share common features such as ischemic placental disease but also differ in their clinical expression regarding maternal diseases. The reason why IUGRremains isolated in some cases yet is followed by clinical manifestations of PE in other cases remains unexplained. A 40-year old woman, gravida two, para one, experienced early-onset IUGR with a significant increase in the ratio of soluble fms-like tyrosine kinase 1 (sFlt-1) to placental growth factor (PlGF) but, surprisingly, without any maternal clinical manifestations of PE. IUGR and a significant increase in sFlt-1/PlGF ratio without PE raise the issue of a missing factor enabling IUGR, a significant increase in sFlt-1/PlGF ratio, and PE to be linked. TEACHING POINTS: (1) Early-onset IUGR and a significant increase in sFlt-1/PlGF ratio do not necessarily mean the onset of PE. (2) Combining early-onset IUGR and a significant increase in sFlt-1/PlGF ratio without PE raises the question of an additional factor responsible for the onset of PE.

Sections du résumé

BACKGROUND BACKGROUND
Intrauterine growth restriction (IUGR) and preeclampsia (PE) share common features such as ischemic placental disease but also differ in their clinical expression regarding maternal diseases. The reason why IUGRremains isolated in some cases yet is followed by clinical manifestations of PE in other cases remains unexplained.
CASE REPORT METHODS
A 40-year old woman, gravida two, para one, experienced early-onset IUGR with a significant increase in the ratio of soluble fms-like tyrosine kinase 1 (sFlt-1) to placental growth factor (PlGF) but, surprisingly, without any maternal clinical manifestations of PE.
CONCLUSION CONCLUSIONS
IUGR and a significant increase in sFlt-1/PlGF ratio without PE raise the issue of a missing factor enabling IUGR, a significant increase in sFlt-1/PlGF ratio, and PE to be linked. TEACHING POINTS: (1) Early-onset IUGR and a significant increase in sFlt-1/PlGF ratio do not necessarily mean the onset of PE. (2) Combining early-onset IUGR and a significant increase in sFlt-1/PlGF ratio without PE raises the question of an additional factor responsible for the onset of PE.

Identifiants

pubmed: 31085278
pii: S2468-7847(18)30509-9
doi: 10.1016/j.jogoh.2019.05.007
pii:
doi:

Substances chimiques

PGF protein, human 0
Placenta Growth Factor 144589-93-5
FLT1 protein, human EC 2.7.10.1
Vascular Endothelial Growth Factor Receptor-1 EC 2.7.10.1

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

695-697

Informations de copyright

Copyright © 2019. Published by Elsevier Masson SAS.

Auteurs

H Boulanger (H)

Department of Nephrology and Dialysis, clinique de l'Estrée, 93240, Stains, France. Electronic address: henriboulanger@noos.fr.

D Drouin (D)

Department of Gynecology and Obstetrics, clinique de l'Estrée, 93240, Stains, France.

C Largilliere (C)

Department of Gynecology and Obstetrics, clinique de l'Estrée, 93240, Stains, France.

G Lefèvre (G)

Department of Biochemistry, Tenon hospital, 75020, Paris, France.

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Classifications MeSH