Opportunities of Artificial Intelligence in The Detection and Prognosis of Viral Hepatitis in Children

Abstract

This article provides a comprehensive overview of the clinical and laboratory diagnostics of viral hepatitis types (A, B, C, D, E) in children, methods for evaluating viral load, and the potential of artificial intelligence (AI) models for prognosis. It discusses the use of machine learning algorithms like LSTM, GRU, and random forest for analyzing, forecasting, and classifying hepatitis dynamics based on viral load data obtained through serological and molecular testing. Key aspects such as data preparation, platforms, and clinical integration of AI models are also considered.

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Qodirova Dilafruz Abdusamat qizi. (2025). Opportunities of Artificial Intelligence in The Detection and Prognosis of Viral Hepatitis in Children. American Journal Of Applied Science And Technology, 5(06), 8–12. https://doi.org/10.37547/ajast/Volume05Issue06-02
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Abstract

This article provides a comprehensive overview of the clinical and laboratory diagnostics of viral hepatitis types (A, B, C, D, E) in children, methods for evaluating viral load, and the potential of artificial intelligence (AI) models for prognosis. It discusses the use of machine learning algorithms like LSTM, GRU, and random forest for analyzing, forecasting, and classifying hepatitis dynamics based on viral load data obtained through serological and molecular testing. Key aspects such as data preparation, platforms, and clinical integration of AI models are also considered.


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American Journal of Applied Science and Technology

8

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VOLUME

Vol.05 Issue 06 2025

PAGE NO.

8-12

DOI

10.37547/ajast/Volume05Issue06-02



Opportunities of Artificial Intelligence in The Detection
and Prognosis of Viral Hepatitis in Children

Qodirova Dilafruz Abdusamat qizi

2nd-year PhD student at Tashkent University of Information Technologies named after Muhammad al-Khwarizmi, Uzbekistan

Received:

11 April 2025;

Accepted:

07 May 2025;

Published:

09 June 2025

Abstract:

This article provides a comprehensive overview of the clinical and laboratory diagnostics of viral hepatitis

types (A, B, C, D, E) in children, methods for evaluating viral load, and the potential of artificial intelligence (AI)
models for prognosis. It discusses the use of machine learning algorithms like LSTM, GRU, and random forest for
analyzing, forecasting, and classifying hepatitis dynamics based on viral load data obtained through serological and
molecular testing. Key aspects such as data preparation, platforms, and clinical integration of AI models are also
considered.

Keywords:

Viral hepatitis, children, artificial intelligence, machine learning, diagnostics, prognosis, medical AI.

Introduction:

Viral hepatitis in children is a serious health issue, as
these infections can lead to chronic liver diseases,
cirrhosis, and hepatocellular carcinoma. Hepatitis
types A, B, C, D, and E exhibit different clinical courses
in children and require molecular and immunological
tests for diagnosis. In this regard, qPCR, dPCR, ELISA,
CLIA, and newer methods such as NGS and LAMP play
a central role. In addition, the use of artificial
intelligence and machine learning algorithms is
increasing in analyzing viral load over time,
automating result interpretation, and enabling
forecasting. Below is a brief description of the types
of viral hepatitis to provide an overview.

Hepatitis A (HAV): HAV is usually transmitted through
contaminated water or food. It is mostly
asymptomatic in children. It does not progress to a
chronic form and lifelong immunity develops after
recovery. According to WHO, 90% of children under
10 in countries with poor sanitation are infected with
HAV.

Hepatitis B (HBV): Mainly transmitted perinatally or
during childhood through blood and div fluids. It
becomes chronic in 90% of infants and 30

50% of

children aged 1

5. Chronic HBV can lead to cirrhosis

and hepatocellular carcinoma. Its spread is
decreasing thanks to vaccination.

Hepatitis C (HCV): Transmitted through blood. Often
asymptomatic in children, but it progresses to a
chronic stage. Approximately 3.5

5 million children

live with chronic HCV. There are medications for
treatment, but no vaccine is available.

Hepatitis D (HDV): Only infects alongside HBV. It
aggravates chronic HBV and increases the risk of liver
cancer. HDV can be prevented by HBV vaccination.

Hepatitis E (HEV): Transmitted via the fecal-oral
route. It is usually mild in children. Fulminant cases
are rare, mainly dangerous for pregnant women. HEV
vaccines are available in some countries.

Related Research

In recent years, a number of studies have been
conducted on the use of modern technologies,
including artificial intelligence (AI) models, in the
diagnosis and prognosis of viral hepatitis. According
to data from the World Health Organization (WHO),
millions of children worldwide are infected with
hepatitis B and C viruses, with most cases being
asymptomatic and progressing to chronic forms.
Therefore, early detection and monitoring are of
great importance.

Tang et al. (2018) described methods for accurately
determining HBV DNA levels using digital PCR (dPCR)
and real-time qPCR in their research. Similarly,


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Alavian et al. (2016) presented results on the early
detection and monitoring of hepatitis C infections in
children using serological tests.

In terms of AI-based approaches, LSTM (Long Short-
Term Memory) networks proposed by Hochreiter and
Schmidhuber (1997) have been successfully used in
medicine for forecasting time-varying data. Cho et al.
introduced the GRU (Gated Recurrent Unit) model,
which is considered lighter and more efficient
compared to LSTM.

Ahmad et al. (2021) developed a random forest
model based on HBV data that predicted the
likelihood of disease progression with high accuracy
(AUC ~0.85). Additionally, it was found that SVM and
LSTM models produced significantly lower error rates
in predicting hepatitis incidence compared to the
ARIMA model.

All of this demonstrates that AI technologies can
enhance medical diagnostics and provide effective
management of hepatitis infection dynamics.
However, for these models to be widely applied in
clinical practice, further research is needed
concerning data quality, ethical standards, and
interpretability challenges.

METHODS

Determining viral hepatitis A, B, C, D, and E in children
and assessing their viral load requires a complex and
multi-step diagnostic process. Traditional serological
and molecular tests provide important clinical
indicators of the patient's condition, but they are not
sufficient to fully analyze or predict changes in viral

load over time. There is a need to use artificial
intelligence models to detect viral load early and
predict the stages of disease development.

Molecular diagnostics (PCR methods): Quantitative
PCR (real-time PCR, qPCR) is used to accurately detect
viral load (such as Hepadnavirus DNA or Flavivirus
RNA) in the blood. qPCR measures the increase in
DNA during the reaction by tracking fluorescence.
Digital PCR (dPCR) divides the sample load into
thousands of individual mini-reactions, each of which
determines whether the virus is present and
calculates the exact copy number. These methods are
used to detect not only HBV DNA, but also HCV and
HDV RNA.

Serological markers: Immunological tests are used to
confirm hepatitis at an early stage. For example, in
hepatitis A and E, the detection of anti-HAV IgM and
anti-HEV IgM antibodies (rapid ELISA/ CLIA) indicates
a recent infection. In hepatitis B, the main markers
are HBsAg (viral surface antigen) and HBeAg (a
marker of high viral activity), the presence of HBsAg
indicates the presence of infection. IgM anti-HBc
indicates a recent B infection. In the diagnosis of
hepatitis C, an anti-HCV antidiv test is first used; if
it is positive, an HCV-RNA (PCR) test is performed.
That is, if anti-HCV is positive, the presence of an
active infection (blood virus) is determined using
RNA-PCR. The clinic also monitors the level of liver
enzymes (ALT, AST), as they indicate liver damage.
Together, these biomarkers provide the basis for
determining viral infection and assessing viral load.

Test type

Biomarkers

Main purpose

Advantages

Disadvantages

Serologik

testlar

(ELISA,

CLIA)

HBsAg, HBeAg,

Anti-HCV, Anti-

HAV IgM, Anti-

HEV IgM

To detect the

presence of the virus

Fast, relatively

affordable, widely used

Does not measure

viral load

precisely,

potential for false

positive/negative

qPCR

(Quantitative

PCR)

HBV DNK, HCV

RNK, HDV RNK

Quantitative

measurement of viral

load

Highly accurate, real-

time measurements,

allows monitoring of

viral dynamics

Expensive,

requires

laboratory

infrastructure

dPCR (Digital

PCR)

HBV DNK, HCV

RNK

Detection of very low

viral loads

High precision, detects

low loads, highly

sensitive

Very expensive,

time-consuming


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NGS (Next-

Generation

Sequencing)

HBV, HCV, HDV

genomes

Genomic profiling of

the virus,

identification of

mutations

Provides complete

genomic data, enables

detection of resistance

mutations

Very expensive,

requires analysis

of large datasets

LAMP (Loop-

mediated

Isothermal

Amplification)

HCV RNK, HBV

DNK

Rapid detection of

viral load

Affordable, quick, does

not require complex

instruments

Less sensitive,

prone to false

positives

ALT/AST

o‘lchovlari

ALT, AST (liver

enzymes)

Evaluation of liver

damage

Affordable, easy to use

Does not detect

viral load, only

indicates liver

damage

FibroScan /

FibroTest

Liver fibrosis stage

Assessment of liver

tissue damage

Non-invasive, easy to

apply

Does not measure

viral load, only

assesses liver

condition

Table 1. Serological and molecular diagnostics of viral hepatitis types

In addition, there are several artificial intelligence
models for the detection of viral hepatitis. LSTM
(Long Short-Term Memory) network: This is a type of
recurrent neural network specifically designed for
working with sequential data (time series). An LSTM
network learns long-term relationships between data
over time. For example, LSTM is useful for predicting
future viral levels based on previously obtained viral
loads and clinical indicators in children. An LSTM

consists of a single cell, in which the “input”, “forget”
and “output” capabilities control the flow of

information. With the help of these capabilities, the
network remembers the important signal and
discards unnecessary information, thus making
predictions based on the time series.

GRU (Gated Recurrent Unit): GRU is also a type of
RNN designed for sequential data like LSTM, but its
internal structure is somewhat simpler. It consists

only of “update” and “forget” capabilities, so it has

fewer parameters. GRU also learns long-term
relationships between data, but is computationally
lighter than LSTM.

Regression models: Simple regression (linear
regression) is used to study linear relationships in
data. For example, it is possible to predict the amount
of virus (count) based on the ALT level of children,
age, and other clinical parameters. Logistic regression
predicts the outcome in terms of binary (infected/not
infected). Regression models are intuitive and fast,
but may sometimes not be sufficient to model
complex time series well.

Other ML methods: Classical algorithms such as
decision trees and random forests, SVM, and k-NN
have also been applied to hepatitis data. For example,
in one study, a random forest model based on
laboratory parameters predicted the development of
HBV disease with high accuracy (AUC ~0.85).
However, nonlinear models such as LSTM and SVM
performed better in predicting hepatitis incidence
than classical ARIMA (LSTM showed the lowest error).
Since the problem of viral load prediction is usually
related to the analysis of time-varying data, RNN
models such as LSTM/GRU are preferable.

Model type

Task type

Advantages

Disadvantages

Best application area

LSTM / GRU

Time series

analysis,

forecasting

Learns long-term

dependencies,

understands dynamic

Learns long-term

dependencies,

understands dynamic

Forecasting viral load

over time


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Model type

Task type

Advantages

Disadvantages

Best application area

changes

changes

CNN

(Convolutional

Neural Network)

Image analysis,

segmentation

Automatic feature

extraction, high

accuracy

Requires large datasets

and GPUs

Detecting liver

diseases from biopsy

images

Transformer

(BERT, GPT)

Text analysis, NLP

Parallel processing,

deep contextual

understanding

Requires massive data

and computational

resources

Analyzing clinical

notes related to viral

load

Random Forest

Classification,

regression

Low risk of

overfitting, easy to

interpret

Slows down with many

trees

Classifying hepatitis

types based on clinical

features

XGBoost /

LightGBM

Classification,

regression, forecast

Very fast, high

accuracy, handles

noise well

Hard to learn, many

parameters

Exploring relationships

between parameters for

viral load prediction

AutoML (H2O.ai,

AutoKeras)

Model creation and

optimization

Easy to use, no-code

ML, rapid prototyping

Limited for complex

datasets

Building simple

models to predict

hepatitis viral load

ARIMA /

SARIMA

Time series

analysis

Simple, intuitive,

effective for small

datasets

Not suitable for non-

linear data

Month-by-month

forecasting of hepatitis

viral load

SVM (Support

Vector Machine)

Classification,

regression

Good for non-linear

data, high accuracy

Slow with large

datasets

Classifying viral load

into low/high levels

DNN (Deep

Neural Network)

Complex

classification and

prediction

Learns complex

relationships, high

accuracy

Requires very large

datasets

Predicting hepatitis

based on multiple

biomarkers

FastAPI / Flask

Model deployment

Easy API

development,

convenient integration

Not suitable for

complex scaling

Creating APIs for viral

load prediction

Docker /

Kubernetes

Model

containerization

and scaling

Easy integration,

independent execution

Complex to learn

Deploying AI models

for large-scale data

environments

Table 2. Types of Artificial Intelligence Models and their Applications

RESULTS

Data Types: The data used in the prediction model
consist of clinical and laboratory parameters. Clinical
parameters

include children’s age, gender, medical

history, symptoms, and physical examination results;
laboratory parameters include liver enzymes (ALT,
AST), hematological parameters (hemoglobin, plt),
viral biomarkers (HBV DNA, HCV RNA), and other
tests; and time-series variables include the above


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parameters obtained from multiple measurements.
Longitudinal data (e.g., viral levels at hospital
admission) are processed using a time-series model.

Data Preparation: First, beginners need to clean the
data: fill in missing or incorrect values (e.g., with
previous or subsequent data), remove unnecessary
columns, and check for anomalous values. Numerical
data (e.g., ALT scores) are normalized (standardized,
normalized)

this is important for machine learning.

Categorical data (e.g., gender, symptoms) should be
converted to a numeric format (one-hot encode or
numeric codes). If there is a time series, the data is
sorted in time order and, if necessary, processed
together with indicators obtained over a period of
time. If the database is large, it is also useful to first

select the “most important” columns (feature

selection).

Tools for building and training AI models

AutoML tools: For beginners in the software industry,
there are AutoML platforms (e.g., H2O.ai, TPOT,
AutoKeras, AutoGluon, Ludwig, and others). These
tools automatically analyze the data, select the most
suitable model, and make it easy to adjust its
parameters (hyperparameter tuning). For example,
TPOT offers tree-based optimization, and AutoKeras
offers auto-building of graph block-type neural
networks.

Python libraries: The most commonly used libraries
for AI and ML model building are scikitlearn (simple
regression, classification, preprocessing), pandas and
NumPy (data analysis and preparation), TensorFlow
and Keras or PyTorch (building differentiated neural
network architectures). For new learners, scikit-learn
has a lighter interface and is convenient for quickly
testing statistical machine learning and regression
models. It is easy to experiment with these tools in
the Jupyter Notebook environment. It is also
recommended to use matplotlib or seaborn for data
visualization.

Brief programming environments: If you do not want
to write code, there are also graphical interface
platforms such as Google AutoML, Azure AutoML for
beginners. They allow you to visually control the
machine learning process. However, for advanced
research, it is usually preferable to work with the
above Python libraries.

CONCLUSION

Molecular and serological tests play a crucial role in
the analysis of viral load, but their predictive value is
limited. Artificial intelligence models, especially LSTM
and GRU, show high efficiency in forecasting taking
into account time variability. Classical ML algorithms
such as Random Forest can be a tool for automating
diagnostics and assisting doctors. However, the
application of AI models in healthcare poses
challenges in terms of data security, clinical
validation, and interpretation.

In the future, AI-based decision-making systems are
expected to be widely implemented in clinical
practice, but this process should be carried out with
caution.

REFERENCES

World Health Organization (WHO). Hepatitis A.

https://www.who.int/news-room/fact-
sheets/detail/hepatitis-a

World Health Organization (WHO). Hepatitis B.

https://www.who.int/news-room/fact-
sheets/detail/hepatitis-b

World Health Organization (WHO). Hepatitis C.

https://www.who.int/news-room/fact-
sheets/detail/hepatitis-c

WHO. Hepatitis D and E.

https://www.who.int/news-

room/fact-sheets/detail/hepatitis-d

Tang et al., “Digital PCR and real

-time PCR in detecting

HBV DNA,” Journal of Clinical Viro

logy, 2018.

Alavian SM et al. "Epidemiology of Hepatitis C in
children." Pediatrics Infect Dis J, 2016.

Hochreiter & Schmidhuber. “Long Short

-Term

Memory.” Neural Computation, 1997.

Cho et al., “Learning Phrase Representations using

RNN Encoder

De

coder,” arXiv, 2014.

Breiman, L. “Random Forests.” Machine Learning,

2001.

Ahmad et al., “Machine learning methods for
predicting hepatitis.” Health Informatics Journal,

2021.

AutoML platforms. Google, H2O.ai, AutoKeras
documentation.

Chollet F. Deep Learning with Python. Manning, 2018.

Pedregosa et al., “Scikit

-learn: Machine Learning in

Python.” JMLR, 2011.

References

World Health Organization (WHO). Hepatitis A. https://www.who.int/news-room/fact-sheets/detail/hepatitis-a

World Health Organization (WHO). Hepatitis B. https://www.who.int/news-room/fact-sheets/detail/hepatitis-b

World Health Organization (WHO). Hepatitis C. https://www.who.int/news-room/fact-sheets/detail/hepatitis-c

WHO. Hepatitis D and E. https://www.who.int/news-room/fact-sheets/detail/hepatitis-d

Tang et al., “Digital PCR and real-time PCR in detecting HBV DNA,” Journal of Clinical Virology, 2018.

Alavian SM et al. "Epidemiology of Hepatitis C in children." Pediatrics Infect Dis J, 2016.

Hochreiter & Schmidhuber. “Long Short-Term Memory.” Neural Computation, 1997.

Cho et al., “Learning Phrase Representations using RNN Encoder–Decoder,” arXiv, 2014.

Breiman, L. “Random Forests.” Machine Learning, 2001.

Ahmad et al., “Machine learning methods for predicting hepatitis.” Health Informatics Journal, 2021.

AutoML platforms. Google, H2O.ai, AutoKeras documentation.

Chollet F. Deep Learning with Python. Manning, 2018.

Pedregosa et al., “Scikit-learn: Machine Learning in Python.” JMLR, 2011.