Machine Learning in Infectious Disease for Risk Factor Identification and Hypothesis Generation: Proof of Concept Using Invasive Candidiasis

Author:

Mayer Lisa M1,Strich Jeffrey R2,Kadri Sameer S2,Lionakis Michail S3,Evans Nicholas G4,Prevots D Rebecca5,Ricotta Emily E5ORCID

Affiliation:

1. Office of Data Science and Emerging Technologies, Office of Science Management and Operations, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH) , Rockville, Maryland , USA

2. Critical Care Medicine Department, NIH Clinical Center, NIH , Bethesda, Maryland , USA

3. Fungal Pathogenesis Section, Laboratory of Clinical Immunology & Microbiology (LCIM), NIAID, NIH , Bethesda, Maryland , USA

4. Department of Philosophy, University of Massachusetts Lowell , Lowell, Maryland , USA

5. Epidemiology and Population Studies Unit, LCIM, NIAID, NIH , Bethesda, Maryland , USA

Abstract

Abstract Background Machine learning (ML) models can handle large data sets without assuming underlying relationships and can be useful for evaluating disease characteristics, yet they are more commonly used for predicting individual disease risk than for identifying factors at the population level. We offer a proof of concept applying random forest (RF) algorithms to Candida-positive hospital encounters in an electronic health record database of patients in the United States. Methods Candida-positive encounters were extracted from the Cerner HealthFacts database; invasive infections were laboratory-positive sterile site Candida infections. Features included demographics, admission source, care setting, physician specialty, diagnostic and procedure codes, and medications received before the first positive Candida culture. We used RF to assess risk factors for 3 outcomes: any invasive candidiasis (IC) vs non-IC, within-species IC vs non-IC (eg, invasive C. glabrata vs noninvasive C. glabrata), and between-species IC (eg, invasive C. glabrata vs all other IC). Results Fourteen of 169 (8%) variables were consistently identified as important features in the ML models. When evaluating within-species IC, for example, invasive C. glabrata vs non-invasive C. glabrata, we identified known features like central venous catheters, intensive care unit stay, and gastrointestinal operations. In contrast, important variables for invasive C. glabrata vs all other IC included renal disease and medications like diabetes therapeutics, cholesterol medications, and antiarrhythmics. Conclusions Known and novel risk factors for IC were identified using ML, demonstrating the hypothesis-generating utility of this approach for infectious disease conditions about which less is known, specifically at the species level or for rarer diseases.

Funder

Division of Intramural Research of the National Institute of Allergy and Infectious Diseases

National Institutes of Health Clinical Center

National Institute of Allergy and Infectious Diseases

US Department of Energy

NIAID

National Science Foundation

Greenwall Foundation Faculty Scholars Program

Davis Educational Foundation

US Air Force Office of Scientific Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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