Evidence map›Paper›PMID 22559298›Full record

ArticleBMC medical genomics2012

Novel biomarker combination improves the diagnosis of serious bacterial infections in Malawian children.

Adam D Irwin, Fiona Marriage, Limangeni A Mankhambo, IPD Group Study, Graham Jeffers, Ruwanthi Kolamunnage-Dona, Malcolm Guiver, Brigitte Denis, Elizabeth M Molyneux, Malcolm E Molyneux and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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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

12 authors at 6 institutions in 2 countries.

Adam D IrwinDepartment of Women's and Children's Health, University of Liverpool, Liverpool, UK. edcarrol@liv.ac.uk
Fiona Marriage
Limangeni A Mankhambo
IPD Group Study
Graham Jeffers
Ruwanthi Kolamunnage-Dona
Malcolm Guiver
Brigitte Denis
Elizabeth M Molyneux
Malcolm E Molyneux
Philip J Day
Enitan D Carrol
University of Liverpool · GBMalawi-Liverpool-Wellcome Trust Clinical Research Programme · MWUniversity of Malawi · MWUniversity of Manchester · GBGreater Manchester Police · GBLiverpool Women's Hospital · GB

Funding

Department of Health RC-PG-0309-10053Wellcome Trust 068026
6 · The paper itself

Abstract

backgroundHigh throughput technologies offer insight into disease processes and heightens opportunities for improved diagnostics. Using transcriptomic analyses, we aimed to discover and to evaluate the clinical validity of a combination of reliable and functionally important biomarkers of serious bacterial infection (SBI).

methodsWe identified three previously reported biomarkers of infection (neutrophil gelatinase-associated lipocalin (NGAL), granulysin and resistin) and measured gene expression using quantitative real-time PCR. Protein products related to the three transcripts were measured by immunoassays.

resultsRelative gene expression values of NGAL and resistin were significantly increased, and expression of granulysin significantly decreased in cases compared to controls. Plasma concentrations of NGAL and resistin were significantly increased in children with confirmed SBI compared to children with no detectable bacterial infection (NBI), and to controls (287 versus 128 versus 62 ng/ml and 195 versus 90 versus 18 ng/ml, respectively, p < 0.05). Plasma protein concentrations of NGAL and resistin were significantly increased in non-survivors compared to survivors (306 versus 211 and 214 versus 150 ng/ml, p = 0.02). The respective areas under the curve (AUC) for NGAL, resistin and procalcitonin in predicting SBI were 0.79, 0.80 and 0.86, whilst a combination of NGAL, resistin and procalcitonin achieved an AUC of 0.90.

conclusionsWe have demonstrated a unique combination of diagnostic biomarkers of SBI using transcriptomics, and demonstrated translational concordance with the corresponding protein. The addition of NGAL and resistin protein measurement to procalcitonin significantly improved the diagnosis of SBI.

Indexed as

Acute-Phase ProteinsAntigens, Differentiation, T-LymphocyteBacterial InfectionsBiomarkersCalcitoninCalcitonin Gene-Related PeptideCase-Control StudiesChildChild, PreschoolFemaleGene Expression RegulationHumansInfantLipocalin-2LipocalinsMalawiAcute-Phase ProteinsAntigens, Differentiation, T-LymphocyteBiomarkersCALCA protein, humanCalcitoninCalcitonin Gene-Related PeptideGNLY protein, humanLCN2 protein, humanLipocalin-2LipocalinsProtein PrecursorsProto-Oncogene ProteinsResistin

Identifiers

PMID22559298
PMCPMC3528639
OpenAlexW2149017714

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.