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  4. Personalized prediction of esophageal cancer risk based on virtually generated alcohol data.
 
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Personalized prediction of esophageal cancer risk based on virtually generated alcohol data.

Journal
Journal of translational medicine
Journal Volume
23
Journal Issue
1
Start Page
論文號碼 379
ISSN
1479-5876
Date Issued
2025-12
Author(s)
Nfor, Oswald Ndi
PEI-MING HUANG  
Wu, Ming-Fang
KE-CHENG CHEN  
Chou, Ying-Hsiang
MONG-WEI LIN  
Zhong, Ji-Han
SHUENN-WEN KUO  
Lee, Yu-Kwang
CHIH-HUNG HSU  
JANG-MING LEE  
Liaw, Yung-Po
DOI
10.1186/s12967-025-06383-9
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/729274
Abstract
Background: Esophageal cancer (EC) presents a significant public health challenge globally, particularly in regions with high alcohol consumption. Its etiology is multifactorial, involving both genetic predispositions and lifestyle factors. Methods: This study aimed to develop a personalized risk prediction model for EC by integrating genetic polymorphisms (rs671 and rs1229984) with virtually generated alcohol consumption data, utilizing advanced artificial intelligence and machine learning techniques. We analyzed data from 86,845 individuals, including 763 diagnosed EC patients, sourced from the Taiwan Biobank. Eight machine learning models were employed: Bayesian Network, Decision Tree, Ensemble, Gradient Boosting, Logistic Regression, LASSO, Random Forest, and Support Vector Machines (SVM). A unique aspect of our approach was the virtual generation of alcohol consumption data, allowing us to evaluate risk profiles under both consuming and non-consuming scenarios. Results: Our analysis revealed that individuals with the genotypes rs671 = AG and rs1229984 = CC exhibited the highest probabilities of developing EC, with values ranging from 0.2041 to 0.9181. Notably, abstaining from alcohol could decrease their risk by approximately 16.29-49.58%. The Ensemble model demonstrated exceptional performance, achieving an area under the curve (AUC) of 0.9577 and a sensitivity of 0.9211. This transition from consumption to abstinence indicated a potential risk reduction of nearly 50% for individuals with high-risk genotypes. Conclusion: Overall, our findings highlight the importance of integrating virtually generated alcohol data for more precise personalized risk assessments for EC.
Subjects
Cancers
Esophagus
Personalized medicine
Predictive medicine
Risk assessment
SDGs

[SDGs]SDG3

Publisher
BioMed Central Ltd
Type
journal article

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