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Machine learning models based on fluid immunoproteins that predict non-AIDS adverse events in people with HIV.
Premeaux, Thomas A; Bowler, Scott; Friday, Courtney M; Moser, Carlee B; Hoenigl, Martin; Lederman, Michael M; Landay, Alan L; Gianella, Sara; Ndhlovu, Lishomwa C.
Afiliación
  • Premeaux TA; Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Bowler S; Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Friday CM; Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Moser CB; Center for Biostatistics in AIDS Research in the Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Hoenigl M; Division of Infectious Diseases, Department of Medicine, University of California San Diego, San Diego, CA, USA.
  • Lederman MM; Division of Infectious Diseases, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Landay AL; Department of Medicine, Division of Infectious Diseases and HIV Medicine, Case Western Reserve University, Cleveland, OH, USA.
  • Gianella S; Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
  • Ndhlovu LC; Division of Infectious Diseases, Department of Medicine, University of California San Diego, San Diego, CA, USA.
iScience ; 27(6): 109945, 2024 Jun 21.
Article en En | MEDLINE | ID: mdl-38812553
ABSTRACT
Despite the success of antiretroviral therapy (ART), individuals with HIV remain at risk for experiencing non-AIDS adverse events (NAEs), including cardiovascular complications and malignancy. Several surrogate immune biomarkers in blood have shown predictive value in predicting NAEs; however, composite panels generated using machine learning may provide a more accurate advancement for monitoring and discriminating NAEs. In a nested case-control study, we aimed to develop machine learning models to discriminate cases (experienced an event) and matched controls using demographic and clinical characteristics alongside 49 plasma immunoproteins measured prior to and post-ART initiation. We generated support vector machine (SVM) classifier models for high-accuracy discrimination of individuals aged 30-50 years who experienced non-fatal NAEs at pre-ART and one-year post-ART. Extreme gradient boosting generated a high-accuracy model at pre-ART, while K-nearest neighbors performed poorly all around. SVM modeling may offer guidance to improve disease monitoring and elucidate potential therapeutic interventions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: IScience Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: IScience Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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