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Detection of microbial invasion of the amniotic cavity by analysis of cervicovaginal proteins in women with preterm labor and intact membranes

Authors :
C. Andrew Combs
Thomas J. Garite
Jodi A. Lapidus
Jerome P. Lapointe
Michael Gravett
Julie Rael
Erol Amon
Jason K. Baxter
Kim Brady
William Clewell
Keith A. Eddleman
Stephen Fortunato
Albert Franco
David M. Haas
Kent Heyborne
Durlin E. Hickok
Helen Y. How
David Luthy
Hugh Miller
Michael Nageotte
Leonardo Pereira
Richard Porreco
Peter A. Robilio
Hyagriv Simhan
Scott A. Sullivan
Kenneth Trofatter
Thomas Westover
Kimberly Maurel
Diana Abril
Source :
American Journal of Obstetrics and Gynecology. 212:482.e1-482.e12
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Objective Microbial invasion of the amniotic cavity (MIAC) is common in early preterm labor and is associated with maternal and neonatal infectious morbidity. MIAC is usually occult and is reliably detected only with amniocentesis. We sought to develop a noninvasive test to predict MIAC based on protein biomarkers in cervicovaginal fluid (CVF) in a cohort of women with preterm labor (phase 1) and to validate the test in an independent cohort (phase 2). Study Design This was a prospective study of women with preterm labor who had amniocentesis to screen for MIAC. MIAC was defined by positive culture and/or 16S ribosomal DNA results. Nine candidate CVF proteins were analyzed by enzyme-linked immunosorbent assay. Logistic regression was used to identify combinations of up to 3 proteins that could accurately classify the phase 1 cohort (N = 108) into those with or without MIAC. The best models, selected by area under the curve (AUC) of the receiver operating characteristic curve in phase 1, included various combinations of interleukin (IL)-6, chemokine (C-X-C motif) ligand 1 (CXCL1), alpha fetoprotein, and insulin-like growth factor binding protein-1. Model performance was then tested in the phase 2 cohort (N = 306). Results MIAC was present in 15% of cases in phase 1 and 9% in phase 2. A 3-marker CVF model using IL-6 plus CXCL1 plus insulin-like growth factor binding protein-1 had AUC 0.87 in phase 1 and 0.78 in phase 2. Two-marker models using IL-6 plus CXCL1 or alpha fetoprotein plus CXCL1 performed similarly in phase 2 (AUC 0.78 and 0.75, respectively), but were not superior to CVF IL-6 alone (AUC 0.80). A cutoff value of CVF IL-6 ≥463 pg/mL (which had 81% sensitivity in phase 1) predicted MIAC in phase 2 with sensitivity 79%, specificity 78%, positive predictive value 38%, and negative predictive value 97%. Conclusion High levels of IL-6 in CVF are strongly associated with MIAC. If developed into a bedside test or rapid laboratory assay, cervicovaginal IL-6 might be useful in selecting patients in whom the probability of MIAC is high enough to warrant amniocentesis or transfer to a higher level of care. Such a test might also guide selection of potential subjects for treatment trials.

Details

ISSN :
00029378
Volume :
212
Database :
OpenAIRE
Journal :
American Journal of Obstetrics and Gynecology
Accession number :
edsair.doi.dedup.....b92170a4deb5c7e62c3fb9fb7e0b8991
Full Text :
https://doi.org/10.1016/j.ajog.2015.02.007