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dc.contributor.authorVajrychova, Marie
dc.contributor.authorStráník, Jaroslav
dc.contributor.authorPimková, Kristýna
dc.contributor.authorBarman, Malin
dc.contributor.authorKukla, Rudolf
dc.contributor.authorZedníková, Petra
dc.contributor.authorBolehovska, Radka
dc.contributor.authorPliskova, Lenka
dc.contributor.authorHornychova, Helena
dc.contributor.authorAndrys, Citrad
dc.contributor.authorTambor, Vojtěch
dc.contributor.authorLenčo, Juraj
dc.contributor.authorJacobsson, Bo
dc.contributor.authorKacerovsky, Marian
dc.date.accessioned2021-03-26T12:25:52Z
dc.date.available2021-03-26T12:25:52Z
dc.date.created2021-03-24T16:10:57Z
dc.date.issued2020
dc.identifier.citationScientific Reports. 2020, .
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/11250/2735742
dc.description.abstractPreterm prelabour rupture of membranes beyond the 34th week of gestation (late PPROM) is frequently associated with the risk of the microbial invasion of the amniotic fluid (MIAC) and histological chorioamnionitis (HCA). Hence, we employed a Tandem Mass Tag-based approach to uncover amniotic fluid proteome response to the presence of MIAC and HCA in late PPROM. Protein dysregulation was associated with only five cases in the group of 15 women with confirmed MIAC and HCA. Altogether, 138 amniotic fluid proteins were changed in these five cases exclusively. These proteins were particularly associated with excessive neutrophil responses to infection, such as neutrophil degranulation and extracellular trap formation. We believe that the quantification of these proteins in amniotic fluid may assist in revealing women with the highest risk of excessive inflammatory response in late PPROM.
dc.language.isoeng
dc.titleComprehensive proteomic investigation of infectious and inflammatory changes in late preterm prelabour rupture of membranes
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber14
dc.source.journalScientific Reports
dc.identifier.doi10.1038/s41598-020-74756-9
dc.identifier.cristin1900772
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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