Multisite validation of a host response signature for predicting likelihood of bacterial and viral infections in patients with suspected influenza.

bacterial classifier gene expression signatures host response influenza point of care predict viral

Journal

European journal of clinical investigation
ISSN: 1365-2362
Titre abrégé: Eur J Clin Invest
Pays: England
ID NLM: 0245331

Informations de publication

Date de publication:
May 2023
Historique:
revised: 08 12 2022
received: 12 10 2022
accepted: 05 01 2023
medline: 11 4 2023
pubmed: 25 1 2023
entrez: 24 1 2023
Statut: ppublish

Résumé

Indiscriminate use of antimicrobials and antimicrobial resistance is a public health threat. IMX-BVN-1, a 29-host mRNA classifier, provides two separate scores that predict likelihoods of bacterial and viral infections in patients with suspected acute infections. We validated the performance of IMX-BVN-1 in adults attending acute health care settings with suspected influenza. We amplified 29-host response genes in RNA extracted from blood by NanoString nCounter. IMX-BVN-1 calculated two scores to predict probabilities of bacterial and viral infections. Results were compared against the infection status (no infection; highly probable/possible infection; confirmed infection) determined by clinical adjudication. Amongst 602 adult patients (74.9% ED, 16.9% ICU, 8.1% outpatients), 7.6% showed in-hospital mortality and 15.5% immunosuppression. Median IMX-BVN-1 bacterial and viral scores were higher in patients with confirmed bacterial (0.27) and viral (0.62) infections than in those without bacterial (0.08) or viral (0.21) infection, respectively. The AUROC distinguishing bacterial from nonbacterial illness was 0.81 and 0.87 when distinguishing viral from nonviral illness. The bacterial top quartile's positive likelihood ratio (LR) was 4.38 with a rule-in specificity of 88%; the bacterial bottom quartile's negative LR was 0.13 with a rule-out sensitivity of 96%. Similarly, the viral top quartile showed an infinite LR with rule-in specificity of 100%; the viral bottom quartile had a LR of 0.22 and a rule-out sensitivity of 85%. IMX-BVN-1 showed high accuracy for differentiating bacterial and viral infections from noninfectious illness in patients with suspected influenza. Clinical utility of IMX-BVN will be validated following integration into a point of care system.

Sections du résumé

BACKGROUND BACKGROUND
Indiscriminate use of antimicrobials and antimicrobial resistance is a public health threat. IMX-BVN-1, a 29-host mRNA classifier, provides two separate scores that predict likelihoods of bacterial and viral infections in patients with suspected acute infections. We validated the performance of IMX-BVN-1 in adults attending acute health care settings with suspected influenza.
METHOD METHODS
We amplified 29-host response genes in RNA extracted from blood by NanoString nCounter. IMX-BVN-1 calculated two scores to predict probabilities of bacterial and viral infections. Results were compared against the infection status (no infection; highly probable/possible infection; confirmed infection) determined by clinical adjudication.
RESULTS RESULTS
Amongst 602 adult patients (74.9% ED, 16.9% ICU, 8.1% outpatients), 7.6% showed in-hospital mortality and 15.5% immunosuppression. Median IMX-BVN-1 bacterial and viral scores were higher in patients with confirmed bacterial (0.27) and viral (0.62) infections than in those without bacterial (0.08) or viral (0.21) infection, respectively. The AUROC distinguishing bacterial from nonbacterial illness was 0.81 and 0.87 when distinguishing viral from nonviral illness. The bacterial top quartile's positive likelihood ratio (LR) was 4.38 with a rule-in specificity of 88%; the bacterial bottom quartile's negative LR was 0.13 with a rule-out sensitivity of 96%. Similarly, the viral top quartile showed an infinite LR with rule-in specificity of 100%; the viral bottom quartile had a LR of 0.22 and a rule-out sensitivity of 85%.
CONCLUSION CONCLUSIONS
IMX-BVN-1 showed high accuracy for differentiating bacterial and viral infections from noninfectious illness in patients with suspected influenza. Clinical utility of IMX-BVN will be validated following integration into a point of care system.

Identifiants

pubmed: 36692131
doi: 10.1111/eci.13957
doi:

Substances chimiques

RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13957

Subventions

Organisme : Inflammatix Inc.
Organisme : The Nepean Institute of Critical Care Education and Research.

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation.

Références

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Auteurs

Maryam Shojaei (M)

Department of Medicine, Sydney Medical School Nepean, Nepean Hospital, University of Sydney, Penrith, New South Wales, Australia.
Department of Intensive Care Medicine, Nepean Hospital, Penrith, New South Wales, Australia.
Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Westmead, New South Wales, Australia.

Uan-I Chen (UI)

Inflammatix, Inc., Sunnyvale, California, USA.

Uros Midic (U)

Inflammatix, Inc., Sunnyvale, California, USA.

Simone Thair (S)

Inflammatix, Inc., Sunnyvale, California, USA.

Sally Teoh (S)

Department of Intensive Care Medicine, Nepean Hospital, Penrith, New South Wales, Australia.

Anthony McLean (A)

Department of Intensive Care Medicine, Nepean Hospital, Penrith, New South Wales, Australia.

Timothy E Sweeney (TE)

Inflammatix, Inc., Sunnyvale, California, USA.

Matthew Thompson (M)

Inflammatix, Inc., Sunnyvale, California, USA.

Oliver Liesenfeld (O)

Inflammatix, Inc., Sunnyvale, California, USA.

Purvesh Khatri (P)

Inflammatix, Inc., Sunnyvale, California, USA.

Benjamin Tang (B)

Department of Intensive Care Medicine, Nepean Hospital, Penrith, New South Wales, Australia.
Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Westmead, New South Wales, Australia.

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