Bacteria localization and chorion thinning among preterm premature rupture of membranes.

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Murtha, AP

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Fortner, KB

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Grotegut, CA

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Ransom, CE

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Bentley, RC

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Feng, L

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Lan, L

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Heine, RP

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Seed, PC

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Sun, Kang

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United States

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2014-01-09T17:05:04Z

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2014

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OBJECTIVE: Bacterial colonization of the fetal membranes and its role in pathogenesis of membrane rupture is poorly understood. Prior retrospective work revealed chorion layer thinning in preterm premature rupture of membranes (PPROM) subjects. Our objective was to prospectively examine fetal membrane chorion thinning and to correlate to bacterial presence in PPROM, preterm, and term subjects. STUDY DESIGN: Paired membrane samples (membrane rupture and membrane distant) were prospectively collected from: PPROM = 14, preterm labor (PTL = 8), preterm no labor (PTNL = 8), term labor (TL = 10), and term no labor (TNL = 8), subjects. Sections were probed with cytokeratin to identify fetal trophoblast layer of the chorion using immunohistochemistry. Fluorescence in situ hybridization was performed using broad range 16 s ribosomal RNA probe. Images were evaluated, chorion and choriodecidua were measured, and bacterial fluorescence scored. Chorion thinning and bacterial presence were compared among and between groups using Student's t-test, linear mixed effect model, and Poisson regression model (SAS Cary, NC). RESULTS: In all groups, the fetal chorion cellular layer was thinner at rupture compared to distant site (147.2 vs. 253.7 µm, p<0.0001). Further, chorion thinning was greatest among PPROM subjects compared to all other groups combined, regardless of site sampled [PPROM(114.9) vs. PTL(246.0) vs. PTNL(200.8) vs. TL(217.9) vs. TNL(246.5)]. Bacteria counts were highest among PPROM subjects compared to all other groups regardless of site sampled or histologic infection [PPROM(31) vs. PTL(9) vs. PTNL(7) vs. TL(7) vs. TNL(6)]. Among all subjects at both sites, bacterial counts were inversely correlated with chorion thinning, even excluding histologic chorioamnionitis (p<0.0001 and p = 0.05). CONCLUSIONS: Fetal chorion was uniformly thinner at rupture site compared to distant sites. In PPROM fetal chorion, we demonstrated pronounced global thinning. Although cause or consequence is uncertain, bacterial presence is greatest and inversely correlated with chorion thinning among PPROM subjects.

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http://www.ncbi.nlm.nih.gov/pubmed/24421883

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PONE-D-13-13497

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1932-6203

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https://hdl.handle.net/10161/8299

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eng

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PLoS

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PLoS One

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10.1371/journal.pone.0083338

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Adult

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Amnion

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Bacteria

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Chorion

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Colony Count, Microbial

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Fetal Membranes, Premature Rupture

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Gestational Age

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Humans

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Immunohistochemistry

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In Situ Hybridization, Fluorescence

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Least-Squares Analysis

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Bacteria localization and chorion thinning among preterm premature rupture of membranes.

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Journal article

duke.contributor.orcid

Grotegut, CA|0000-0002-3511-7642

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Bentley, RC|0000-0002-4947-9150

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Feng, L|0000-0002-2936-7397

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/24421883

pubs.begin-page

e83338

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1

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Basic Science Departments

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Clinical Science Departments

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Duke

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Duke Cancer Institute

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Global Health Institute

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Institutes and Centers

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Institutes and Provost's Academic Units

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Midwifery Service

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Molecular Genetics and Microbiology

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Obstetrics and Gynecology

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Obstetrics and Gynecology, Maternal Fetal Medicine

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Pathology

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Pediatrics

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Pediatrics, Infectious Diseases

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School of Medicine

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Surgery

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Surgery, Urology

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University Institutes and Centers

pubs.publication-status

Published online

pubs.volume

9

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