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Machine Learning Applied to Omics Datasets Predicts Mortality in Patients with Alcoholic Hepatitis.
Gao, Bei; Wu, Tsung-Chin; Lang, Sonja; Jiang, Lu; Duan, Yi; Fouts, Derrick E; Zhang, Xinlian; Tu, Xin-Ming; Schnabl, Bernd.
Afiliação
  • Gao B; School of Marine Sciences, Nanjing University of Information Science and Technology, Nanjing 210044, China.
  • Wu TC; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA.
  • Lang S; Department of Mathematics, University of California San Diego, San Diego, CA 92093, USA.
  • Jiang L; Division of Biostatistics and Bioinformatics, Herbert Wertheim School of Public Health, University of California San Diego, San Diego, CA 92093, USA.
  • Duan Y; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA.
  • Fouts DE; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA.
  • Zhang X; Department of Medicine, VA San Diego Healthcare System, San Diego, CA 92161, USA.
  • Tu XM; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA.
  • Schnabl B; J. Craig Venter Institute, Rockville, MD 20850, USA.
Metabolites ; 12(1)2022 Jan 05.
Article em En | MEDLINE | ID: mdl-35050163
ABSTRACT
Alcoholic hepatitis is a major health care burden in the United States due to significant morbidity and mortality. Early identification of patients with alcoholic hepatitis at greatest risk of death is extremely important for proper treatments and interventions to be instituted. In this study, we used gradient boosting, random forest, support vector machine and logistic regression analysis of laboratory parameters, fecal bacterial microbiota, fecal mycobiota, fecal virome, serum metabolome and serum lipidome to predict mortality in patients with alcoholic hepatitis. Gradient boosting achieved the highest AUC of 0.87 for both 30-day mortality prediction using the bacteria and metabolic pathways dataset and 90-day mortality prediction using the fungi dataset, which showed better performance than the currently used model for end-stage liver disease (MELD) score.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Metabolites Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Metabolites Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China