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dc.date.accessioned2015-11-26T18:59:17Z
dc.date.available2015-11-26T18:59:17Z
dc.date.created2015-07-02T14:16:16Z
dc.date.issued2015
dc.identifier.citationHolme, Ane Moe Paasche, Cecilie Lorentzen, Bjørg Michelsen, Trond Melbye Henriksen, Tore . Placental glucose transfer: A human in vivo study. PLoS ONE. 2015, 10(2)
dc.identifier.urihttp://hdl.handle.net/10852/47891
dc.description.abstractObjectives The placental transfer of nutrients is influenced by maternal metabolic state, placenta function and fetal demands. Human in vivo studies of this interplay are scarce and challenging. We aimed to establish a method to study placental nutrient transfer in humans. Focusing on glucose, we tested a hypothesis that maternal glucose concentrations and uteroplacental arterio-venous difference (reflecting maternal supply) determines the fetal venous-arterial glucose difference (reflecting fetal consumption). Methods Cross-sectional in vivo study of 40 healthy women with uncomplicated term pregnancies undergoing planned caesarean section. Glucose and insulin were measured in plasma from maternal and fetal sides of the placenta, at the incoming (radial artery and umbilical vein) and outgoing vessels (uterine vein and umbilical artery). Results There were significant mean (SD) uteroplacental arterio-venous 0.29 (0.23) mmol/L and fetal venous-arterial 0.38 (0.31) mmol/L glucose differences. The transplacental maternal-fetal glucose gradient was 1.22 (0.42) mmol/L. The maternal arterial glucose concentration was correlated to the fetal venous glucose concentration (r = 0.86, p<0.001), but not to the fetal venous-arterial glucose difference. The uteroplacental arterio-venous glucose difference was neither correlated to the level of glucose in the umbilical vein, nor fetal venous-arterial glucose difference. The maternal-fetal gradient was correlated to fetal venous-arterial glucose difference (r = 0.8, p<0.001) and the glucose concentration in the umbilical artery (r = −0.45, p = 0.004). Glucose and insulin concentrations were correlated in the mother (r = 0.52, p = 0.001), but not significantly in the fetus. We found no significant correlation between maternal and fetal insulin values. Conclusions We did not find a relation between indicators of maternal glucose supply and the fetal venous-arterial glucose difference. Our findings indicate that the maternal-fetal glucose gradient is significantly influenced by the fetal venous-arterial difference and not merely dependent on maternal glucose concentration or the arterio-venous difference on the maternal side of the placenta.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherPublic Library of Science (PLoS)
dc.relation.ispartofHolme, Ane Moe (2018) Studies of the human placenta in vivo -The role of the placenta in glucose transfer and secretion of anti-angiogenic factors. Doctoral thesis. http://hdl.handle.net/10852/61898
dc.relation.urihttp://hdl.handle.net/10852/61898
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titlePlacental glucose transfer: A human in vivo studyen_US
dc.typeJournal articleen_US
dc.creator.authorHolme, Ane Moe
dc.creator.authorPaasche, Cecilie
dc.creator.authorLorentzen, Bjørg
dc.creator.authorMichelsen, Trond Melbye
dc.creator.authorHenriksen, Tore
cristin.unitcode185,53,13,10
cristin.unitnameObstetrikk og gynekologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1252213
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS ONE&rft.volume=10&rft.spage=&rft.date=2015
dc.identifier.jtitlePLoS ONE
dc.identifier.volume10
dc.identifier.issue2
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pone.0117084
dc.identifier.urnURN:NBN:no-51906
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1932-6203
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/47891/1/journal.pone.0117084.pdf
dc.type.versionPublishedVersion
cristin.articleide0117084


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