Predictive value of cervical cytokine, antimicrobial and microflora levels for pre-term birth in high-risk women

Spontaneous preterm birth (sPTB, delivery <37 weeks gestation), accounts for approximately 10% of births worldwide; the aetiology is multifactorial with intra-amniotic infection being one contributing factor. This study aimed to determine whether asymptomatic women with a history of sPTB or cervi...

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Published inScientific reports Vol. 9; no. 1; pp. 11246 - 11
Main Authors Manning, Rashmi, James, Catherine P., Smith, Marie C., Innes, Barbara A., Stamp, Elaine, Peebles, Donald, Bajaj-Elliott, Mona, Klein, Nigel, Bulmer, Judith N., Robson, Stephen C., Lash, Gendie E.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 02.08.2019
Nature Publishing Group
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ISSN2045-2322
2045-2322
DOI10.1038/s41598-019-47756-7

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Summary:Spontaneous preterm birth (sPTB, delivery <37 weeks gestation), accounts for approximately 10% of births worldwide; the aetiology is multifactorial with intra-amniotic infection being one contributing factor. This study aimed to determine whether asymptomatic women with a history of sPTB or cervical surgery have altered levels of inflammatory/antimicrobial mediators and/or microflora within cervical fluid at 22–24 weeks gestation. External cervical fluid was collected from women with history of previous sPTB and/or cervical surgery at 22–24 weeks gestation (n = 135). Cytokine and antimicrobial peptides were measured on a multiplex platform or by ELISA. qPCR was performed for detection of 7 potentially pathogenic bacterial species. IL-8 and IL-1β levels were lower in women who delivered preterm compared to those who delivered at term (IL-8 P  = 0.02; IL-1β P  = 0.04). There were no differences in elafin or human beta defensin-1 protein levels between the two groups. Multiple bacterial species were detected in a higher proportion of women who delivered preterm than in those who delivered at term ( P  = 0.005). Cervical fluid IL-8 and IL-1β and microflora have the potential to be used as biomarkers to predict sPTB in high risk women.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-019-47756-7