Evidence map›Paper›PMID 40627636›Full record

ArticlePloS one2025

Enhancing diabetes risk prediction through focal active learning and machine learning models.

Wangyouchen Zhang, Zhenhua Xia, Guoqing Cai, Junhao Wang, Xutao Dong

Abstract read
In one paragraph

Article in PloS one, 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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

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

5 authors.

Wangyouchen ZhangSchool of Electronic Information and Electrical Engineering, Yangtze University, Jingzhou, China.
Zhenhua XiaSchool of Electronic Information and Electrical Engineering, Yangtze University, Jingzhou, China.ORCID https://orcid.org/0000-0001-7466-7391
Guoqing CaiSchool of Electronic Information and Electrical Engineering, Yangtze University, Jingzhou, China.
Junhao WangSchool of Electronic Information and Electrical Engineering, Yangtze University, Jingzhou, China.
Xutao DongSchool of Electronic Information and Electrical Engineering, Yangtze University, Jingzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To improve the effectiveness of diabetes risk prediction, this study proposes a novel method based on focal active learning strategies combined with machine learning models. Existing machine learning models often suffer from poor performance on imbalanced medical datasets, where minority class instances such as diabetic cases are underrepresented. Our proposed Focal Active Learning method selectively samples informative instances to mitigate this imbalance, leading to better prediction outcomes with fewer labeled samples. The method integrates SHAP (SHapley Additive Explanations) to quantify feature importance and applies attention mechanisms to dynamically adjust feature weights, enhancing model interpretability and performance in predicting diabetes risk. To address the issue of imbalanced classification in diabetes datasets, we employed a clustering-based method to identify representative data points (called foci), and iteratively constructed a smaller labeled dataset (sub-pool) around them using similarity-based sampling. This method aims to overcome common challenges, such as poor performance on minority classes and limited generalization, by enabling more efficient data utilization and reducing labeling costs. The experimental results demonstrated that our approach significantly improved the evaluation metrics for diabetes risk prediction, achieving an accuracy of 97.41% and a recall rate of 94.70%, clearly outperforming traditional models that typically achieve 95% accuracy and 92% recall. Additionally, the model's generalization ability was further validated on the public PIMA Indians Diabetes DataBase, outperforming traditional models in both accuracy and recall. This approach can enhance early diabetes screening in clinical settings, helping healthcare professionals reduce diagnostic errors and optimize resource allocation.

Indexed as

Diabetes MellitusMachine LearningFemaleHumansMaleRisk AssessmentRisk Factors

Identifiers

PMID40627636
PMCPMC12237043

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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.