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Active regression model for clinical grading of COVID-19.
Sh, Yuan; Dong, Jierong; Chen, Zhongqing; Yuan, Meiqing; Lyu, Lingna; Zhang, Xiuli.
  • Sh Y; Fujian Provincial Key Laboratory of Brain Aging and Neurodegenerative Diseases, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian, China.
  • Dong J; The Chinese Academy of Sciences (CAS) Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, The Chinese Academy of Sciences (CAS) Key Laboratory of Standardization and Measurement for Nanotechnology, The Chinese Academy of Sciences (CAS) Center for Excellence in Nanoscience, Nationa
  • Chen Z; The Chinese Academy of Sciences (CAS) Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, The Chinese Academy of Sciences (CAS) Key Laboratory of Standardization and Measurement for Nanotechnology, The Chinese Academy of Sciences (CAS) Center for Excellence in Nanoscience, Nationa
  • Yuan M; The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
  • Lyu L; Key Laboratory of Forensic Genetics, Institute of Forensic Sciences, Ministry of Public Security, Beijing, China.
  • Zhang X; Department of Gastroenterology and Hepatology, Beijing You'an Hospital, Capital Medical University, Beijing, China.
Front Immunol ; 14: 1141996, 2023.
Artículo en Inglés | MEDLINE | ID: covidwho-2303437
ABSTRACT

Background:

In the therapeutic process of COVID-19, the majority of indicators that physicians have for assisting treatment have come from clinical tests represented by proteins, metabolites, and immune levels in patients' blood. Therefore, this study constructs an individualized treatment model based on deep learning methods, aiming to realize timely intervention based on clinical test indicator data of COVID-19 patients and provide an important theoretical basis for optimizing medical resource allocation.

Methods:

This study collected clinical data from a total of 1,799 individuals, including 560 controls for non-respiratory infectious diseases (Negative), 681 controls for other respiratory virus infections (Other), and 558 coronavirus infections (Positive) for COVID-19. We first used the Student T-test to screen for statistically significant differences (Pvalue<0.05); we then used the Adaptive-Lasso method stepwise regression to screen the characteristic variables and filter the features with low importance; we then used analysis of covariance to calculate the correlation between variables and filter the highly correlated features; and finally, we analyzed the feature contribution and screened the best combination of features.

Results:

Feature engineering reduced the feature set to 13 feature combinations. The correlation coefficient between the projected results of the artificial intelligence-based individualized diagnostic model and the fitted curve of the actual values in the test group was 0.9449 which could be applied to the clinical prognosis of COVID-19. In addition, the depletion of platelets in patients with COVID-19 is an important factor affecting their severe deterioration. With the progression of COVID-19, there is a slight decrease in the total number of platelets in the patient's body, particularly as the volume of larger platelets sharply decreases. The importance of plateletCV (count*mean platelet volume) in evaluating the severity of COVID-19 patients is higher than the count of platelets and mean platelet volume.

Conclusion:

In general, we found that for patients with COVID-19, the increase in mean platelet volume was a predictor for SARS-Cov-2. The rapid decrease of platelet volume and the decrease of total platelet volume are dangerous signals for the aggravation of SARS-Cov-2 infection. The analysis and modeling results of this study provide a new perspective for individualized accurate diagnosis and treatment of clinical COVID-19 patients.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Estudios diagnósticos / Estudio experimental / Estudio pronóstico Límite: Humanos Idioma: Inglés Revista: Front Immunol Año: 2023 Tipo del documento: Artículo País de afiliación: Fimmu.2023.1141996

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Estudios diagnósticos / Estudio experimental / Estudio pronóstico Límite: Humanos Idioma: Inglés Revista: Front Immunol Año: 2023 Tipo del documento: Artículo País de afiliación: Fimmu.2023.1141996