Evidence map›Paper›PMID 42898138›Full record

ArticleFrontiers in endocrinology2026

A primary care-oriented framework for osteoporosis prediction: integrating multi-algorithm feature selection and machine learning model benchmarking.

Xiaofang Guan, Xiaoqi Wang, Wenjing Zhang, Juanjuan Li, Zhili Hou, Zhaoting Hu, Pei Sun

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Xiaofang Guan *Health Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Xiaoqi Wang *Health Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Wenjing ZhangHealth Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Juanjuan LiHealth Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Zhili HouHealth Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Zhaoting HuHealth Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Pei SunHealth Management Center, the Third Affiliated Hospital of Southern Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Summary: Large-scale screening and primary care diagnosis of osteoporosis are challenging due to the limited availability of dual-energy X-ray absorptiometry (DXA). Therefore, predictive models for osteoporosis that do not rely on bone mineral density measurements are essential. Using routine health examination data and applying a consensus feature selection strategy, we constructed machine learning (ML)-based models and compared their performance across multiple dimensions. Purpose: To develop a robust, low-cost, and interpretable framework for osteoporosis prediction based on readily available information, which can be easily integrated into electronic health systems to inform DXA referral in resource-limited settings. Methods: Variables covered by the basic health examination package were obtained from participants who underwent health examinations between January 2024 and January 2025. We implemented a strategy in which only features selected by at least four out of the seven feature selection methods were retained. Six ML algorithms were employed to develop models, and their prediction performances were compared across discrimination, goodness-of-fit, and clinical utility. Results: A total of 2,260 participants were included, with an osteoporosis prevalence of 7.1%. Eight features: age, sex, body mass index, alkaline phosphatase, hematocrit, high-density lipoprotein, urea, and platelet count, were selected for model development. In the validation set, the random forest and artificial neural network (ANN) models demonstrated strongest screening performance, with AUCs of 0.895 (95% CI 0.867-0.923) and 0.890 (95% CI 0.862-0.919), respectively. The ANN model additionally exhibited superior calibration. Shapley additive explanations were applied to interpret the ANN model for osteoporosis prediction. Conclusion: This study presents an easily integrable model for osteoporosis prediction based on routine health examination data. The ANN model provides robust prediction, offering a potential tool for pre-DXA triage and early identification of high-risk individuals in primary care and resource-limited settings.

Indexed as

AlgorithmsBenchmarkingMachine LearningOsteoporosisPrimary Health CareAbsorptiometry, PhotonAgedBone DensityFemaleHumansMaleMiddle AgedPrediction AlgorithmsPredictive Learning Modelsdual-energy X-ray absorptiometrymachine learningosteoporosispredictive modelprimary care

Identifiers

PMID42898138
PMCPMC13677370

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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.