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


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
02 08 2019
Historique:
received: 14 03 2019
accepted: 10 07 2019
entrez: 4 8 2019
pubmed: 4 8 2019
medline: 11 11 2020
Statut: epublish

Résumé

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.

Identifiants

pubmed: 31375740
doi: 10.1038/s41598-019-47756-7
pii: 10.1038/s41598-019-47756-7
pmc: PMC6677789
doi:

Substances chimiques

Antimicrobial Cationic Peptides 0
Biomarkers 0
Cytokines 0
DNA, Bacterial 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11246

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT097228MA
Pays : United Kingdom

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Auteurs

Rashmi Manning (R)

Reproductive and Vascular Biology Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

Catherine P James (CP)

Research Department of Maternal and Fetal Medicine, Institute for Women's Health, University College London, London, UK.
Infection, Immunity, Inflammation and Physiological Medicine, Institute of Child Health, University College London, London, UK.

Marie C Smith (MC)

Reproductive and Vascular Biology Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

Barbara A Innes (BA)

Reproductive and Vascular Biology Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

Elaine Stamp (E)

Institue of Health and Society, Newcastle University, Newcastle upon Tyne, UK.

Donald Peebles (D)

Research Department of Maternal and Fetal Medicine, Institute for Women's Health, University College London, London, UK.

Mona Bajaj-Elliott (M)

Infection, Immunity, Inflammation and Physiological Medicine, Institute of Child Health, University College London, London, UK.

Nigel Klein (N)

Infection, Immunity, Inflammation and Physiological Medicine, Institute of Child Health, University College London, London, UK.

Judith N Bulmer (JN)

Reproductive and Vascular Biology Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

Stephen C Robson (SC)

Reproductive and Vascular Biology Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

Gendie E Lash (GE)

Reproductive and Vascular Biology Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK. gendie.lash@hotmail.com.
Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou, China. gendie.lash@hotmail.com.

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