Evidence map›Paper›PMID 40375096›Full record

ArticleBMC gastroenterology2025

Machine learning for predicting all-cause mortality of metabolic dysfunction-associated fatty liver disease: a longitudinal study based on NHANES.

Xueni Wang, Huihui Chen, Luqiao Wang, Wenguang Sun

Abstract read
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Article in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Xueni WangCenter of Clinical Big Data and Analytics of The Second Affiliated Hospital, and Department of Big Data in Health Science School of Public Health, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310058, China.
Huihui ChenCenter of Clinical Big Data and Analytics of The Second Affiliated Hospital, and Department of Big Data in Health Science School of Public Health, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310058, China.
Luqiao WangCenter of Clinical Big Data and Analytics of The Second Affiliated Hospital, and Department of Big Data in Health Science School of Public Health, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310058, China.
Wenguang SunCenter for Data Science, Zhejiang University, 866 Yuhangtang Rd, Room 1411, Hangzhou, Zhejiang, 310058, China. wgsun@zju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mortality burden of metabolic dysfunction-associated fatty liver disease (MAFLD) is rising, making it crucial to predict mortality and identify the factors influencing it. While advanced machine learning algorithms are gaining recognition as effective tools for clinical prediction, their ability to predict all-cause mortality of MAFLD individuals remains uncertain. This study aimed to develop different machine learning models to predict all-cause mortality of MAFLD individuals, compare the predictive performance of these models, and identify the risk factors contributing all-cause mortality, which is crucial for management of MAFLD individuals.

methodsWe included 3921 MAFLD individuals in NHANES III. After a median follow-up time of 310 months, 1815 (46.3%) deaths were recorded. The data (demographic, behavioral factors and laboratory indicators) were utilized to construct machine learning models (Coxnet, RSF, GBS) after feature selection. Time-dependent AUC, time-dependent brier and C-index were then evaluated the performance of models. We identified the top five factors that contributed significantly to all-cause mortality and further explore the association with all-cause mortality using RCS and Kaplan-Meier survival curves.

resultsCoxnet showed the best performance in short-term and long-term predictions with time-dependent AUC of 0.82 at 5 years and 0.88 at 25 years. Age, FORNS, waist circumstance, AAR, FLI were associated positively with all-cause mortality. Compared to the individuals who smoked more than 100 cigarettes, those below 100 had better survival outcome (P < 0.0001).

conclusionsMachine learning has a promising application in predicting all-cause mortality in MAFLD individuals. Combined the results of interpretable machine learning and association analyses, we found risk factors which contributing to the all-cause mortality. These findings provide insights for community health practitioners to intervene in modifiable risk factors, thereby improving the survival and quality of life of MAFLD individuals.

Indexed as

Fatty LiverMachine LearningNon-alcoholic Fatty Liver DiseaseAdultAgedCause of DeathFemaleHumansKaplan-Meier EstimateLongitudinal StudiesMaleMiddle AgedNutrition SurveysRisk FactorsAll-cause mortalityFatty liverMachine learningMetabolic dysfunction-associated fatty liver disease

Identifiers

PMID40375096
PMCPMC12082853

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.