Evidence map›Paper›PMID 32379834›Full record

ArticlePloS one2020

Mid-trimester amniotic fluid proteome's association with spontaneous preterm delivery and gestational duration.

Maria Hallingström, Petra Zedníková, Vojtěch Tambor, Malin Barman, Marie Vajrychová, Juraj Lenčo, Felicia Viklund, Linda Tancred, Hardis Rabe, Daniel Jonsson and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Systematic review of preterm birth multi-omic biomarker studies.Expert reviews in molecular medicine · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 8 institutions in 4 countries.

Maria HallingströmDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Petra ZedníkováBiomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.ORCID 0000-0002-8245-1897
Vojtěch TamborBiomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Malin BarmanDepartment of Biology and Biological Engineering, Food and Nutrition Science, Chalmers University of Technology, Gothenburg, Sweden.
Marie VajrychováBiomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Juraj LenčoBiomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Felicia ViklundDepartment of Obstetrics and Gynecology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Linda TancredDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Hardis RabeDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Daniel JonssonDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Alisa KachikisDepartment of Obstetrics and Gynecology, University of Washington, Seattle, Washington, USA.
Staffan NilssonDepartment of Mathematical Sciences, Chalmers University of Technology, Gothenburg, Sweden.
Marian KacerovskýBiomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Kristina M Adams WaldorfDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-6939-7224
Bo JacobssonDepartment of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0001-5079-2374
Sahlgrenska University Hospital · SEChalmers University of Technology · SECharles University · CZUniversity Hospital Hradec Králové · CZUniversity of Washington · USNorwegian Institute of Public Health · NOUniversity of Gothenburg · SEUniversity of Pardubice · CZ

Funding

Role of the hyaluronidase in GBS VirulenceR01AI133976 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI ADAMS WALDORF, KRISTINA M., RAJAGOPAL, LAKSHMI · 2017 to 2021
$4.5M
Immune Control of Group B Streptococcal PlacentalR01AI145890 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI ADAMS WALDORF, KRISTINA M., RAJAGOPAL, LAKSHMI · 2019 to 2023
$4.4M
NIAID NIH HHS R01 AI133976NIAID NIH HHS R01 AI145890
6 · The paper itself

Abstract

backgroundAmniotic fluid is clinically accessible via amniocentesis and its protein composition may correspond to birth timing. Early changes in the amniotic fluid proteome could therefore be associated with the subsequent development of spontaneous preterm delivery.

objectiveThe main objective of this study was to perform unbiased proteomics analysis of the association between mid-trimester amniotic fluid proteome and spontaneous preterm delivery and gestational duration, respectively. A secondary objective was to validate and replicate the findings by enzyme-linked immunosorbent assay using a second independent cohort.

methodsWomen undergoing a mid-trimester genetic amniocentesis at Sahlgrenska University Hospital/Östra between September 2008 and September 2011 were enrolled in this study, designed in three analytical stages; 1) an unbiased proteomic discovery phase using LC-MS analysis of 22 women with subsequent spontaneous preterm delivery (cases) and 37 women who delivered at term (controls), 2) a validation phase of proteins of interest identified in stage 1, and 3) a replication phase of the proteins that passed validation using a second independent cohort consisting of 20 cases and 40 matched controls.

resultsNine proteins were nominally significantly associated with both spontaneous preterm delivery and gestational duration, after adjustment for gestational age at sampling, but none of the proteins were significant after correction for multiple testing. Several of these proteins have previously been described as being associated with spontaneous PTD etiology and six of them were thus validated using enzyme linked immunosorbent assay. Two of the proteins passed validation; Neutrophil gelatinase-associated lipocalin and plasminogen activator inhibitor 1, but the results could not be replicated in a second cohort.

conclusionsNeutrophil gelatinase-associated lipocalin and Plasminogen activator inhibitor 1 are potential biomarkers of spontaneous preterm delivery and gestational duration but the findings could not be replicated. The negative findings are supported by the fact that none of the nine proteins from the exploratory phase were significant after correction for multiple testing.

Indexed as

Gestational AgeAdultAmniocentesisAmniotic FluidCohort StudiesFemaleHumansMalePregnancyPregnancy Trimester, SecondPremature BirthProteomeProteome

Identifiers

PMID32379834
PMCPMC7205297
OpenAlexW3021567255

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.