Objective The aim of this study is to develop a machine learning (ML) model to accurately predict liver enzyme elevation in rheumatoid arthritis (RA) patients on treatment with methotrexate (MTX) using electronic health record (EHR) data from a real-world RA cohort. Methods Demographic, clinical, biochemical, and prescription information from 569 RA patients initiated on MTX were collected retrospectively. The primary outcome was the liver transaminase elevation above the upper limit of normal (40 IU/mL), following the initiation of MTX. The total dataset was randomly split into a training (80%) and test set (20%) and used to develop a random forest classifier model. The best model was selected after hyper-parameter tuning and fivefold cross-validation. Results A total of 104 (18.2%) patients developed elevated transaminase while on MTX therapy. The best-performing predictive model had an accuracy/F1 score of 0.87. The top 10 predictive features were then used to create a limited feature model that retained most of the predictive accuracy, with an accuracy/F1 score of 0.86. Baseline high-normal transaminase levels, and higher lymphocyte and neutrophil blood count proportions were the highest predictors of elevated transaminase levels after MTX therapy. Conclusion Our proof-of-concept study suggests the possibility of building a well-performing ML model to predict liver transaminase elevation in RA patients being treated with MTX. Similar ML models could be used to identify "high-risk" patients and target them for early stratification.
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http://dx.doi.org/10.7759/cureus.52110 | DOI Listing |
Alzheimers Dement
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Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, U.S.A., Philadelphia, PA, USA.
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A 9-year-old neutered male cairn terrier dog was initially presented because of inappetence, increased respiratory effort, and occasional coughing. A cavitary lung mass was diagnosed using CT and removed with lung lobectomy. Histopathology of the mass revealed necrosuppurative inflammation with acid-fast rod bacteria in macrophages, with spp.
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January 2025
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Metabolic-dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease in the Western world. MASLD-associated cirrhosis prevalence is on the rise along with the obesity and metabolic syndrome epidemic. Genetic factors are included in the multi-hit model of MASLD pathogenesis and insulin-like growth factor-1 (IGF-1) has an important role.
View Article and Find Full Text PDFZhonghua Wei Zhong Bing Ji Jiu Yi Xue
December 2024
Department of Anesthesiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu, China. Corresponding author: Rao Zhuqing, Email:
Macrophages are widely distributed in peripheral blood, lungs, liver, brain, kidneys, skin, testes, vascular endothelial cells, and other parts of the body. As sentinel cells of innate immunity, they play an important role in the occurrence and development of sepsis. Recent research in immune metabolism has revealed the complicated relationship between specific metabolic pathways of macrophages and their phenotype and function in sepsis.
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