Evidence map›Paper›PMID 30958855›Full record

ArticlePloS one2019

A host gene expression approach for identifying triggers of asthma exacerbations.

Emily C Lydon, Charles Bullard, Mert Aydin, Olga M Better, Anna Mazur, Bradly P Nicholson, Emily R Ko, Micah T McClain, Geoffrey S Ginsburg, Chris W Woods and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 8 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

13 authors at 2 institutions in 1 country.

Emily C LydonDuke University School of Medicine, Durham, NC, United States of America.ORCID 0000-0003-3510-6254
Charles BullardDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Mert AydinDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Olga M BetterDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Anna MazurDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Bradly P NicholsonDurham Veterans Affairs Health Care System, Durham, NC, United States of America.
Emily R KoDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.ORCID 0000-0003-0542-3750
Micah T McClainDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Geoffrey S GinsburgDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Chris W WoodsDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.
Thomas W BurkeDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.ORCID 0000-0003-0592-5822
Ricardo HenaoDuke University Department of Biostatistics and Informatics, Durham, NC, United States of America.
Ephraim L TsalikDuke University Center for Applied Genomics and Precision Medicine, Durham, NC, United States of America.ORCID 0000-0002-6417-2042
Duke University · USDurham VA Health Care System · US

Funding

Antibacterial Resistance Leadership Group (ARLG)UM1AI104681 · NIAID · DUKE UNIVERSITY · PI Vance G. Fowler, Henry F HENRY CHAMBERS · 2013 to 2026
$180.8M
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
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
NIAID NIH HHS U01 AI066569NIAID NIH HHS UM1 AI104681NIH HHS S10 OD018164
6 · The paper itself

Abstract

rationaleAsthma exacerbations often occur due to infectious triggers, but determining whether infection is present and whether it is bacterial or viral remains clinically challenging. A diagnostic strategy that clarifies these uncertainties could enable personalized asthma treatment and mitigate antibiotic overuse.

objectivesTo explore the performance of validated peripheral blood gene expression signatures in discriminating bacterial, viral, and noninfectious triggers in subjects with asthma exacerbations.

methodsSubjects with suspected asthma exacerbations of various etiologies were retrospectively selected for peripheral blood gene expression analysis from a pool of subjects previously enrolled in emergency departments with acute respiratory illness. RT-PCR quantified 87 gene targets, selected from microarray-based studies, followed by logistic regression modeling to define bacterial, viral, or noninfectious class. The model-predicted class was compared to clinical adjudication and procalcitonin.

resultsOf 46 subjects enrolled, 7 were clinically adjudicated as bacterial, 18 as viral, and 21 as noninfectious. Model prediction was congruent with clinical adjudication in 15/18 viral and 13/21 noninfectious cases, but only 1/7 bacterial cases. None of the adjudicated bacterial cases had confirmatory microbiology; the precise etiology in this group was uncertain. Procalcitonin classified only one subject in the cohort as bacterial. 47.8% of subjects received antibiotics.

conclusionsOur model classified asthma exacerbations by the underlying bacterial, viral, and noninfectious host response. Compared to clinical adjudication, the majority of discordances occurred in the bacterial group, due to either imperfect adjudication or model misclassification. Bacterial infection was identified infrequently by all classification schemes, but nearly half of subjects were prescribed antibiotics. A gene expression-based approach may offer useful diagnostic information in this population and guide appropriate antibiotic use.

Indexed as

AdolescentAdultAgedAged, 80 and overAnti-Bacterial AgentsAsthmaBacterial InfectionsChildCohort StudiesEmergency Service, HospitalFemaleGene ExpressionHumansMaleMiddle AgedModels, BiologicalAnti-Bacterial AgentsProcalcitonin

Identifiers

PMID30958855
PMCPMC6453459
OpenAlexW2936742838

What OpenQuestion holds

Textmetadata
LicenceCC0
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.