Evidence map›Paper›PMID 18622029›Full record

ArticleMolecular & cellular proteomics : MCP2008

Identification of diagnostic biomarkers for infection in premature neonates.

Stephen F Kingsmore, Neil Kennedy, Henry L Halliday, Jennifer C Van Velkinburgh, Shengiang Zhong, Vanessa Gabriel, Judith Grant, William D Beavis, Velizar T Tchernev, Lorah Perlee and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Investigation of salivary C-reactive protein and interleukin-18 for the diagnosis of neonatal sepsis.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2021
    Article
  6. Targeting IL-17A attenuates neonatal sepsis mortality induced by IL-18.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  7. Biological functions of thyroid hormone in placenta.International journal of molecular sciences · 2015
    Review
  8. Time for a neonatal-specific consensus definition for sepsis.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Biomarkers for pediatric sepsis and septic shock.Expert review of anti-infective therapy · 2011
    Review
  20. Article
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

14 authors at 5 institutions in 2 countries.

Stephen F KingsmoreNational Center for Genome Resources, Santa Fe, New Mexico, 87505, USA. sfk@ncgr.org
Neil Kennedy
Henry L Halliday
Jennifer C Van Velkinburgh
Shengiang Zhong
Vanessa Gabriel
Judith Grant
William D Beavis
Velizar T Tchernev
Lorah Perlee
Serguei Lejnine
Brian Grimwade
Martin Sorette
J David M Edgar
Iowa State University · USNational Center for Genome Resources · USQueen's Medical Centre · GBRoyal Jubilee Maternity Services · GBUniversity of Ulster · GB

Funding

Plasma Protein Biomarker-Based Diagnostics Of Outcome In Sepsis and CAPU01AI066569 · NIAID · NATIONAL CENTER FOR GENOME RESOURCES · PI KINGSMORE, STEPHEN FRANCIS · 2005 to 2010
$2.9M
NIAID NIH HHS AI066569NIAID NIH HHS U01 AI066569
6 · The paper itself

Abstract

Infection is a leading cause of neonatal morbidity and mortality worldwide. Premature neonates are particularly susceptible to infection because of physiologic immaturity, comorbidity, and extraneous medical interventions. Additionally premature infants are at higher risk of progression to sepsis or severe sepsis, adverse outcomes, and antimicrobial toxicity. Currently initial diagnosis is based upon clinical suspicion accompanied by nonspecific clinical signs and is confirmed upon positive microbiologic culture results several days after institution of empiric therapy. There exists a significant need for rapid, objective, in vitro tests for diagnosis of infection in neonates who are experiencing clinical instability. We used immunoassays multiplexed on microarrays to identify differentially expressed serum proteins in clinically infected and non-infected neonates. Immunoassay arrays were effective for measurement of more than 100 cytokines in small volumes of serum available from neonates. Our analyses revealed significant alterations in levels of eight serum proteins in infected neonates that are associated with inflammation, coagulation, and fibrinolysis. Specifically P- and E-selectins, interleukin 2 soluble receptor alpha, interleukin 18, neutrophil elastase, urokinase plasminogen activator and its cognate receptor, and C-reactive protein were observed at statistically significant increased levels. Multivariate classifiers based on combinations of serum analytes exhibited better diagnostic specificity and sensitivity than single analytes. Multiplexed immunoassays of serum cytokines may have clinical utility as an adjunct for rapid diagnosis of infection and differentiation of etiologic agent in neonates with clinical decompensation.

Indexed as

BiomarkersBlood ProteinsCluster AnalysisDemographyGestational AgeHumansImmunoassayInfant, NewbornInfant, PrematureInfant, Premature, DiseasesInfectionsMultivariate AnalysisBiomarkersBlood Proteins

Identifiers

PMID18622029
PMCPMC2559932
OpenAlexW2146419198

What OpenQuestion holds

Textmetadata
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.