Evidence map›Paper›PMID 36327243›Full record

ArticlePloS one2022

MicroRNA analysis in maternal blood of pregnancies with preterm premature rupture of membranes reveals a distinct expression profile.

Michail Spiliopoulos, Andrew Haddad, Huda B Al-Kouatly, Saeed Haleema, Michael J Paidas, Sara N Iqbal, Robert I Glazer

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 1 country.

Michail SpiliopoulosDepartment of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine and Genetics, University of Miami, Miami, Florida, United States of America.ORCID 0000-0003-1277-7477
Andrew HaddadDepartment of Obstetrics, Gynecology & Women's Health, Division of Maternal Fetal Medicine & Surgery, Hackensack Meridian School of Medicine, Hackensack University Medical Center, Hackensack, New Jersey, United States of America.ORCID 0000-0003-1910-9279
Huda B Al-KouatlyDepartment of Obstetrics and Gynecology, Division of Maternal Fetal Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, United States of America.
Saeed HaleemaDepartment of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine, MedStar Washington Hospital Center, Washington, DC, United States of America.ORCID 0000-0002-6890-0377
Michael J PaidasDepartment of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine and Genetics, University of Miami, Miami, Florida, United States of America.
Sara N IqbalDepartment of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine, MedStar Washington Hospital Center, Washington, DC, United States of America.
Robert I GlazerDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States of America.ORCID 0000-0001-6936-2980
MedStar Washington Hospital Center · USUniversity of Miami · USGeorgetown University · USHackensack University Medical Center · USThomas Jefferson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the expression profile of microRNAs in the peripheral blood of pregnant women with preterm premature rupture of membranes (PPROM) compared to that of healthy pregnant women. STUDY

designThis was a pilot study with case-control design in pregnant patients enrolled between January 2017 and June 2019. Patients with healthy pregnancies and those affected by PPROM between 20- and 33+6 weeks of gestation were matched by gestational age and selected for inclusion to the study. Patients were excluded for multiple gestation and presence of a major obstetrical complication such as preeclampsia, diabetes, fetal growth restriction and stillbirth. A total of ten (n = 10) controls and ten (n = 10) patients with PPROM were enrolled in the study. Specimens were obtained before administration of betamethasone or intravenous antibiotics. MicroRNA expression was analyzed for 800 microRNAs in each sample using the NanoString nCounter Expression Assay. Differential expression was calculated after normalization and log2- transformation using the false discovery rate (FDR) method at an alpha level of 5%.

resultsDemographic characteristics were similar between the two groups. Of the 800 miRNAs analyzed, 116 were differentially expressed after normalization. However, only four reached FDR-adjusted statistical significance. Pregnancies affected by PPROM were characterized by upregulation of miR-199a-5p, miR-130a-3p and miR-26a-5p and downregulation of miR-513b-5p (FDR adjusted p-values <0.05). The differentially expressed microRNAs participate in pathways associated with altered collagen and matrix metalloprotease expression in the extracellular matrix.

conclusionPatients with PPROM have a distinct peripheral blood microRNA profile compared to healthy pregnancies as measured by the NanoString Expression Assay.

Indexed as

MicroRNAsPremature Rupture of Fetal MembranesFemaleGestational AgeHumansInfant, NewbornPilot ProjectsPregnancyPregnancy, MultipleMicroRNAs

Identifiers

PMID36327243
PMCPMC9632843
OpenAlexW4308099805

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.