Validation of a host response test to distinguish bacterial and viral respiratory infection.
dc.contributor.author | Lydon, Emily C | |
dc.contributor.author | Henao, Ricardo | |
dc.contributor.author | Burke, Thomas W | |
dc.contributor.author | Aydin, Mert | |
dc.contributor.author | Nicholson, Bradly P | |
dc.contributor.author | Glickman, Seth W | |
dc.contributor.author | Fowler, Vance G | |
dc.contributor.author | Quackenbush, Eugenia B | |
dc.contributor.author | Cairns, Charles B | |
dc.contributor.author | Kingsmore, Stephen F | |
dc.contributor.author | Jaehne, Anja K | |
dc.contributor.author | Rivers, Emanuel P | |
dc.contributor.author | Langley, Raymond J | |
dc.contributor.author | Petzold, Elizabeth | |
dc.contributor.author | Ko, Emily R | |
dc.contributor.author | McClain, Micah T | |
dc.contributor.author | Ginsburg, Geoffrey S | |
dc.contributor.author | Woods, Christopher W | |
dc.contributor.author | Tsalik, Ephraim L | |
dc.date.accessioned | 2019-11-01T15:05:03Z | |
dc.date.available | 2019-11-01T15:05:03Z | |
dc.date.issued | 2019-10-17 | |
dc.date.updated | 2019-11-01T15:05:02Z | |
dc.description.abstract | BACKGROUND:Distinguishing bacterial and viral respiratory infections is challenging. Novel diagnostics based on differential host gene expression patterns are promising but have not been translated to a clinical platform nor extensively tested. Here, we validate a microarray-derived host response signature and explore performance in microbiology-negative and coinfection cases. METHODS:Subjects with acute respiratory illness were enrolled in participating emergency departments. Reference standard was an adjudicated diagnosis of bacterial infection, viral infection, both, or neither. An 87-transcript signature for distinguishing bacterial, viral, and noninfectious illness was measured from peripheral blood using RT-PCR. Performance characteristics were evaluated in subjects with confirmed bacterial, viral, or noninfectious illness. Subjects with bacterial-viral coinfection and microbiologically-negative suspected bacterial infection were also evaluated. Performance was compared to procalcitonin. FINDINGS:151 subjects with microbiologically confirmed, single-etiology illness were tested, yielding AUROCs 0•85-0•89 for bacterial, viral, and noninfectious illness. Accuracy was similar to procalcitonin (88% vs 83%, p = 0•23) for bacterial vs. non-bacterial infection. Whereas procalcitonin cannot distinguish viral from non-infectious illness, the RT-PCR test had 81% accuracy in making this determination. Bacterial-viral coinfection was subdivided. Among 19 subjects with bacterial superinfection, the RT-PCR test identified 95% as bacterial, compared to 68% with procalcitonin (p = 0•13). Among 12 subjects with bacterial infection superimposed on chronic viral infection, the RT-PCR test identified 83% as bacterial, identical to procalcitonin. 39 subjects had suspected bacterial infection; the RT-PCR test identified bacterial infection more frequently than procalcitonin (82% vs 64%, p = 0•02). INTERPRETATION:The RT-PCR test offered similar diagnostic performance to procalcitonin in some subgroups but offered better discrimination in others such as viral vs. non-infectious illness and bacterial/viral coinfection. Gene expression-based tests could impact decision-making for acute respiratory illness as well as a growing number of other infectious and non-infectious diseases. | |
dc.identifier | S2352-3964(19)30644-9 | |
dc.identifier.issn | 2352-3964 | |
dc.identifier.issn | 2352-3964 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | EBioMedicine | |
dc.relation.isversionof | 10.1016/j.ebiom.2019.09.040 | |
dc.subject | Biomarkers | |
dc.subject | Coinfection | |
dc.subject | Diagnosis | |
dc.subject | Gene expression | |
dc.subject | Precision medicine | |
dc.subject | Respiratory tract infections | |
dc.title | Validation of a host response test to distinguish bacterial and viral respiratory infection. | |
dc.type | Journal article | |
duke.contributor.orcid | Henao, Ricardo|0000-0003-4980-845X | |
duke.contributor.orcid | Burke, Thomas W|0000-0003-0592-5822 | |
duke.contributor.orcid | Fowler, Vance G|0000-0002-8048-0897 | |
duke.contributor.orcid | Ginsburg, Geoffrey S|0000-0003-4739-9808 | |
duke.contributor.orcid | Woods, Christopher W|0000-0001-7240-2453 | |
duke.contributor.orcid | Tsalik, Ephraim L|0000-0002-6417-2042 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Nursing | |
pubs.organisational-group | School of Nursing | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Pathology | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Medicine, Cardiology | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Duke Global Health Institute | |
pubs.organisational-group | University Institutes and Centers | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Medicine, Infectious Diseases | |
pubs.organisational-group | Molecular Genetics and Microbiology | |
pubs.organisational-group | Basic Science Departments | |
pubs.publication-status | Published |
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