Mathematical model of liver cirrhosis formation during morphological and molecular-genetic preclinical studies

BACKGROUND: Currently, researchers describe challenges in developing new treatments for fibrosis and cirrhosis: poor quality of preclinical models, insufficient trial duration, and lack of markers of therapeutic response. A separate task is to standardize the process of liver cirrhosis formation in preclinical trials, which is necessary to obtain accurate quantitative estimates in a short timeframe. AIM: This study aimed to develop a mathematical model for the formation of liver cirrhosis during preclinical trials. MATERIALS AND METHODS: Liver fibrosis and cirrhosis were induced in male Wistar rats using freshly prepared thioacetamide solution for 17 weeks. The area of connective tissue was determined as a percentage of the image area. The area of interlobular veins was measured in µm2. The numbers of cells expressing the FAP marker and the α-SMA marker were counted. The level of mRNA expression of the Vegfa and Yap1 genes was assessed by real-time polymerase chain reaction. A mathematical model for classifying observations into stages was constructed using multiple logistic regression with stepwise selection of predictors, followed by calculation of sensitivity, specificity, and area under the curve with a 95% confidence interval based on ROC analysis. RESULTS: As a result of the analysis, a mathematical model of liver cirrhosis formation was developed. The model is based on the values of two indicators: FAP+ cells and Yap1 mRNA and demonstrated good quality. The resulting value of the area under the ROC curve of 0.883 suggests good results for classifying cases. CONCLUSIONS: The mathematical model makes it possible to differentiate the stage of liver cirrhosis from the stage of fibrosis during preclinical studies. It provides a foundation for studying the pathogenesis of liver fibrosis and cirrhosis, identifying new potential molecular targets for antifibrotic therapy, and reducing the number of expensive, labor-intensive laboratory tests.

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Publication Details

Journal
Morphology
Published
2024-09-05
DOI
https://doi.org/10.17816/morph.632588
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
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article

Mathematical model of liver cirrhosis formation during morphological and molecular-genetic preclinical studies

Е. И. Лебедева, В. Н. Мартинков, Д. А. Зиновкин, A. T. Shchastniy et al.
Morphology
Liver Disease Diagnosis and Treatment
article

Mathematical model of liver cirrhosis formation during morphological and molecular-genetic preclinical studies

Е. И. Лебедева, В. Н. Мартинков, Д. А. Зиновкин, A. T. Shchastniy, A. S. Babenka, Eldar Arkadyevich Nadyrov
article en

Abstract

BACKGROUND: Currently, researchers describe challenges in developing new treatments for fibrosis and cirrhosis: poor quality of preclinical models, insufficient trial duration, and lack of markers of therapeutic response. A separate task is to standardize the process of liver cirrhosis formation in preclinical trials, which is necessary to obtain accurate quantitative estimates in a short timeframe. AIM: This study aimed to develop a mathematical model for the formation of liver cirrhosis during preclinical trials. MATERIALS AND METHODS: Liver fibrosis and cirrhosis were induced in male Wistar rats using freshly prepared thioacetamide solution for 17 weeks. The area of connective tissue was determined as a percentage of the image area. The area of interlobular veins was measured in µm2. The numbers of cells expressing the FAP marker and the α-SMA marker were counted. The level of mRNA expression of the Vegfa and Yap1 genes was assessed by real-time polymerase chain reaction. A mathematical model for classifying observations into stages was constructed using multiple logistic regression with stepwise selection of predictors, followed by calculation of sensitivity, specificity, and area under the curve with a 95% confidence interval based on ROC analysis. RESULTS: As a result of the analysis, a mathematical model of liver cirrhosis formation was developed. The model is based on the values of two indicators: FAP+ cells and Yap1 mRNA and demonstrated good quality. The resulting value of the area under the ROC curve of 0.883 suggests good results for classifying cases. CONCLUSIONS: The mathematical model makes it possible to differentiate the stage of liver cirrhosis from the stage of fibrosis during preclinical studies. It provides a foundation for studying the pathogenesis of liver fibrosis and cirrhosis, identifying new potential molecular targets for antifibrotic therapy, and reducing the number of expensive, labor-intensive laboratory tests.

MorphologyVol. 162(2)
Gomel State Medical University (BY), Vitebsk State Medical University (BY), Republican Research Center for Radiation Medicine and Human Ecology (BY), Belarusian State Medical University (BY)
Openalex Percentile: Top 78%
Liver Disease Diagnosis and Treatment
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