Evidence map›Paper›PMID 27293317›Full record

ArticleMediators of inflammation2016

Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis.

Enrique Segura-Cervantes, Javier Mancilla-Ramírez, Jorge González-Canudas, Erika Alba, René Santillán-Ballesteros, Deneb Morales-Barquet, Gabriela Sandoval-Plata, Norma Galindo-Sevilla

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  7. iScience · 2024
    Article
  8. bioRxiv : the preprint server for biology · 2024
    Article
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  17. Observational
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  20. Sepsis-Induced Immunosuppression in Neonates.Frontiers in pediatrics · 2018
    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

8 authors at 2 institutions in 1 country.

Enrique Segura-CervantesDepartamento de Epidemiología, Instituto Nacional de Perinatología, Secretaría de Salud (SSa), Montes Urales 800, Colonia Lomas de Virreyes, 11000 Mexico City, Mexico.
Javier Mancilla-RamírezEscuela Superior de Medicina (ESM), Instituto Politécnico Nacional (IPN), Avenida Salvador Diaz Miron S/N, Esquina Plan de San Luis, Colonia Casco de Santo Tomás, Delegación Miguel Hidalgo, 11340 Mexico City, Mexico; Hospital de la Mujer, SSa, Prolongación Salvador Diaz Miron 374, Colonia Casco de Santo Tomás, Delegación Miguel Hidalgo, 11340 Mexico City, Mexico.
Jorge González-CanudasLaboratorio Silanes, Amores 1304, Colonia del Valle, 03100 Mexico City, Mexico.
Erika AlbaLaboratorio Silanes, Amores 1304, Colonia del Valle, 03100 Mexico City, Mexico.
René Santillán-BallesterosDepartamento de Infectología e Inmunología, Instituto Nacional de Perinatología, SSa, Montes Urales 800, Colonia Lomas de Virreyes, 11000 Mexico City, Mexico.
Deneb Morales-BarquetUCIREN, Instituto Nacional de Perinatología, SSa, Montes Urales 800, Colonia Lomas de Virreyes, 11000 Mexico City, Mexico.
Gabriela Sandoval-PlataLaboratorio Silanes, Amores 1304, Colonia del Valle, 03100 Mexico City, Mexico.
Norma Galindo-SevillaDepartamento de Infectología e Inmunología, Instituto Nacional de Perinatología, SSa, Montes Urales 800, Colonia Lomas de Virreyes, 11000 Mexico City, Mexico.ORCID 0000-0002-6639-8475
Instituto Nacional de Perinatología · MXInstituto Nacional de las Mujeres · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The response of the adaptive immune system is usually less intense in premature neonates than term neonates. The primary objective of this study was to determine whether immunological parameters vary between preterm (PT) neonates (≥32 weeks of gestational age) and very preterm (VPT) neonates (<32 weeks of gestational age). A cross-sectional study was designed to prospectively follow PT and VPT neonates at risk of developing sepsis. Plasma concentrations of IFN-γ, TNF-α, IL-6, IL-4, and IL-10 were detected using flow cytometry. C-reactive protein (C-RP) and the complex SC5b-9 were detected in the plasma using commercial kits. A total of 83 patients were included. The laboratory results and clinical histories showed that 26 patients had sepsis; 14 were VPT, and 12 were PT. The levels of C-RP, SC5b-9 (innate immune response mediators), and IL-10 or IL-4 (anti-inflammatory cytokines) were elevated during sepsis in both groups. IFN-γ, TNF-α, and IL-6 (proinflammatory cytokines) were differentially elevated only in PT neonates. The VPT neonates with sepsis presented increases in C-RP, SC5b-9, and anti-inflammatory cytokines but not in proinflammatory cytokines, whereas PT neonates showed increases in all studied mediators of inflammation.

Indexed as

Complement Membrane Attack ComplexC-Reactive ProteinCross-Sectional StudiesFemaleHumansImmunity, InnateInfant, Extremely PrematureInfant, NewbornInfant, PrematureInflammationInterferon-gammaInterleukin-10Interleukin-4Interleukin-6MaleSepsisComplement Membrane Attack ComplexC-Reactive ProteinInterferon-gammaInterleukin-10Interleukin-4Interleukin-6SC5b-9 protein complexTumor Necrosis Factor-alpha

Identifiers

PMID27293317
PMCPMC4884838
OpenAlexW2398236882

What OpenQuestion holds

Textmetadata
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.