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Nasopharyngeal metabolomics and machine learning approach for the diagnosis of influenza.
Hogan, Catherine A; Rajpurkar, Pranav; Sowrirajan, Hari; Phillips, Nicholas A; Le, Anthony T; Wu, Manhong; Garamani, Natasha; Sahoo, Malaya K; Wood, Mona L; Huang, ChunHong; Ng, Andrew Y; Mak, Justin; Cowan, Tina M; Pinsky, Benjamin A.
  • Hogan CA; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA; Clinical Virology Laboratory, Stanford Health Care, Palo Alto, CA 94304, USA. Electronic address: catherine.hogan@bccdc.ca.
  • Rajpurkar P; Stanford Computer Science Department, Stanford University, Stanford, CA 94305, USA.
  • Sowrirajan H; Stanford Computer Science Department, Stanford University, Stanford, CA 94305, USA.
  • Phillips NA; Stanford Computer Science Department, Stanford University, Stanford, CA 94305, USA.
  • Le AT; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Wu M; Stanford Department of Anesthesiology, Stanford University, Stanford, CA 94305, USA.
  • Garamani N; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Sahoo MK; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Wood ML; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA; Clinical Virology Laboratory, Stanford Health Care, Palo Alto, CA 94304, USA.
  • Huang C; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Ng AY; Stanford Computer Science Department, Stanford University, Stanford, CA 94305, USA.
  • Mak J; Stanford Biochemical Genetics Laboratory, Stanford Health Care, Palo Alto, CA 94304, USA.
  • Cowan TM; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Biochemical Genetics Laboratory, Stanford Health Care, Palo Alto, CA 94304, USA.
  • Pinsky BA; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA; Clinical Virology Laboratory, Stanford Health Care, Palo Alto, CA 94304, USA; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, C
EBioMedicine ; 71: 103546, 2021 Sep.
Article in English | MEDLINE | ID: covidwho-1363149
ABSTRACT

BACKGROUND:

Respiratory virus infections are significant causes of morbidity and mortality, and may induce host metabolite alterations by infecting respiratory epithelial cells. We investigated the use of liquid chromatography quadrupole time-of-flight mass spectrometry (LC/Q-TOF) combined with machine learning for the diagnosis of influenza infection.

METHODS:

We analyzed nasopharyngeal swab samples by LC/Q-TOF to identify distinct metabolic signatures for diagnosis of acute illness. Machine learning models were performed for classification, followed by Shapley additive explanation (SHAP) analysis to analyze feature importance and for biomarker discovery.

FINDINGS:

A total of 236 samples were tested in the discovery phase by LC/Q-TOF, including 118 positive samples (40 influenza A 2009 H1N1, 39 influenza H3 and 39 influenza B) as well as 118 age and sex-matched negative controls with acute respiratory illness. Analysis showed an area under the receiver operating characteristic curve (AUC) of 1.00 (95% confidence interval [95% CI] 0.99, 1.00), sensitivity of 1.00 (95% CI 0.86, 1.00) and specificity of 0.96 (95% CI 0.81, 0.99). The metabolite most strongly associated with differential classification was pyroglutamic acid. Independent validation of a biomarker signature based on the top 20 differentiating ion features was performed in a prospective cohort of 96 symptomatic individuals including 48 positive samples (24 influenza A 2009 H1N1, 5 influenza H3 and 19 influenza B) and 48 negative samples. Testing performed using a clinically-applicable targeted approach, liquid chromatography triple quadrupole mass spectrometry, showed an AUC of 1.00 (95% CI 0.998, 1.00), sensitivity of 0.94 (95% CI 0.83, 0.98), and specificity of 1.00 (95% CI 0.93, 1.00). Limitations include lack of sample suitability assessment, and need to validate these findings in additional patient populations.

INTERPRETATION:

This metabolomic approach has potential for diagnostic applications in infectious diseases testing, including other respiratory viruses, and may eventually be adapted for point-of-care testing.

FUNDING:

None.
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Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Molecular Diagnostic Techniques / Influenza, Human / Metabolome / Machine Learning Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: English Journal: EBioMedicine Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Molecular Diagnostic Techniques / Influenza, Human / Metabolome / Machine Learning Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: English Journal: EBioMedicine Year: 2021 Document Type: Article