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Potential Peripartum Markers of Infectious-Inflammatory Complications in Spontaneous Preterm Birth
V. Tambor, M. Vajrychova, M. Kacerovsky, M. Link, P. Domasinska, R. Menon, J. Lenco,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT13599
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Free Medical Journals
from 2013
PubMed Central
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Europe PubMed Central
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ProQuest Central
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Open Access Digital Library
from 2001-01-01
Open Access Digital Library
from 2012-12-04
Open Access Digital Library
from 2013-01-01
CINAHL Plus with Full Text (EBSCOhost)
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Health & Medicine (ProQuest)
from 2013
Wiley-Blackwell Open Access Titles
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ROAD: Directory of Open Access Scholarly Resources
from 2013
PubMed
26120581
DOI
10.1155/2015/343501
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Pregnancy Complications, Infectious genetics pathology MeSH
- Humans MeSH
- Peptide Mapping MeSH
- Peripartum Period genetics MeSH
- Amniotic Fluid metabolism MeSH
- Premature Birth genetics pathology MeSH
- Proteome genetics MeSH
- Pregnancy MeSH
- Inflammation complications genetics MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Spontaneous preterm birth significantly contributes to the overall neonatal morbidity associated with preterm deliveries. Nearly 50% of cases are associated with microbial invasion of the amniotic cavity followed by an inflammatory response. Robust diagnostic tools for neonates jeopardized by infection and inflammation may thus decrease the overall neonatal morbidity substantially. Amniotic fluid retrieved during labor retains fetal and pregnancy-related protein fingerprint and its sampling does not place any unwanted stress on women. Using exploratory and targeted methods we analyzed proteomes of amniotic fluid sampled at the end of spontaneous preterm labor prior to delivery from women with and without infection and inflammation. Exploratory data indicated several amniotic fluid proteins to be associated with infectious-inflammatory complications in spontaneous preterm birth. LC-SRM analysis subsequently verified statistically significant changes in lipocalin-1 (P = 0.047 and AUC = 0.67, P = 0.046), glycodelin (P = 0.013 and AUC = 0.73, P = 0.013), and nicotinamide phosphoribosyltransferase (P = 0.018 and AUC = 0.71, P = 0.01).
References provided by Crossref.org
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