Evidence map›Paper›PMID 26270578›Full record

Observational studyPediatric research2015

Serum eotaxin-1 is increased in extremely-low-birth-weight infants with bronchopulmonary dysplasia or death.

Jegen Kandasamy, Claire Roane, Alexander Szalai, Namasivayam Ambalavanan

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in Pediatric research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
0.5field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
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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

4 authors at 1 institution in 1 country.

Jegen KandasamyDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
Claire RoaneDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
Alexander SzalaiDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Namasivayam AmbalavananDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.ORCID http://orcid.org/0000-0003-0731-9092
University of Alabama at Birmingham · US

Funding

Molecular Evolution Strategies to Derive New Recombinant AAV VectorsR01HL092096 · NHLBI · STANFORD UNIVERSITY · PI KAY, MARK A · 2009 to 2012
$2.2M
FcgRIIB links CRP signals with ITGAM functions: a G x G x G model of SLE.R21AR058864 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SZALAI, ALEXANDER J · 2009 to 2010
$783k
MMP-2 in Neonatal Hypoxic Pulmonary Vascular RemodelingK08HD046513 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AMBALAVANAN, NAMASIVAYAM · 2004 to 2008
$608k
C-Reactive Protein in Extremely Low Birth Weight NeonatesR03HD054420 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AMBALAVANAN, NAMASIVAYAM · 2007 to 2008
$144k
NHLBI NIH HHS R01 HL092096NIAMS NIH HHS R21 AR058864NICHD NIH HHS K08 HD 046513NICHD NIH HHS K08 HD046513NICHD NIH HHS R03 HD054420
6 · The paper itself

Abstract

backgroundEarly systemic inflammation in extremely-low-birth-weight (ELBW) infants is associated with an increased risk of bronchopulmonary dysplasia (BPD). Our objective was to identify circulating biomarkers and develop prediction models for BPD/death soon after birth.

methodsBlood samples from postnatal day 1 were analyzed for C-reactive protein (CRP) by enzyme-linked immunosorbent assay and for 39 cytokines/chemokines by a multiplex assay in 152 ELBW infants. The primary outcome was physiologic BPD or death by 36 wk. CRP, cytokines, and clinical variables available at ≤24 h were used for forward stepwise regression and Classification and Regression Tree (CART) analysis to identify predictors of BPD/death.

resultsOverall, 24% developed BPD and 35% died or developed BPD. Regression analysis identified birth weight and eotaxin (CCL11) as the two most significant variables. CART identified FiO2 at 24 h (11% BPD/death if FiO2 ≤28%, 49% if >28%) and eotaxin in infants with FiO2 > 28% (29% BPD/death if eotaxin was ≤84 pg/ml; 65% if >84) as variables most associated with outcome.

conclusionEotaxin measured on the day of birth is useful for identifying ELBW infants at risk of BPD/death. Further investigation is required to determine if eotaxin is involved in lung injury and pathogenesis of BPD.

Indexed as

Age FactorsBiomarkersBirth WeightBronchopulmonary DysplasiaChemokine CCL11C-Reactive ProteinEnzyme-Linked Immunosorbent AssayFemaleHospital MortalityHumansInfantInfant, Extremely Low Birth WeightInfant MortalityInfant, NewbornMaleNeonatal ScreeningBiomarkersCCL11 protein, humanChemokine CCL11C-Reactive Protein

Identifiers

PMID26270578
PMCPMC4628573
OpenAlexW2258717270

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Registered trials

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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.