Evidence map›Paper›PMID 36482780›Full record

ArticleJournal of medical Internet research2023

Interpretable Deep-Learning Approaches for Osteoporosis Risk Screening and Individualized Feature Analysis Using Large Population-Based Data: Model Development and Performance Evaluation.

Bogyeong Suh, Heejin Yu, Hyeyeon Kim, Sanghwa Lee, Sunghye Kong, Jin-Woo Kim, Jongeun Choi

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Article in Journal of medical Internet research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
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28citing papers in PubMed, 1 pooled it
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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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3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Bogyeong Suh *School of Mechanical Engineering, Yonsei University, Seoul, Republic of Korea.ORCID 0000-0002-1725-1258
Heejin Yu *School of Mechanical Engineering, Yonsei University, Seoul, Republic of Korea.ORCID 0000-0003-3986-6939
Hyeyeon KimDepartment of Family Medicine, School of Medicine, Ewha Womans University, Seoul, Republic of Korea.ORCID 0000-0002-5888-9290
Sanghwa LeeDepartment of Family Medicine, School of Medicine, Ewha Womans University, Seoul, Republic of Korea.ORCID 0000-0002-1114-8786
Sunghye KongDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.ORCID 0000-0002-8791-0909
Jin-Woo KimDepartment of Oral and Maxillofacial Surgery, School of Medicine, Ewha Womans University, Seoul, Republic of Korea.ORCID 0000-0002-1672-5730
Jongeun ChoiSchool of Mechanical Engineering, Yonsei University, Seoul, Republic of Korea.ORCID 0000-0002-7532-5315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteoporosis is one of the diseases that requires early screening and detection for its management. Common clinical tools and machine-learning (ML) models for screening osteoporosis have been developed, but they show limitations such as low accuracy. Moreover, these methods are confined to limited risk factors and lack individualized explanation.

objectiveThe aim of this study was to develop an interpretable deep-learning (DL) model for osteoporosis risk screening with clinical features. Clinical interpretation with individual explanations of feature contributions is provided using an explainable artificial intelligence (XAI) technique.

methodsWe used two separate data sets: the National Health and Nutrition Examination Survey data sets from the United States (NHANES) and South Korea (KNHANES) with 8274 and 8680 respondents, respectively. The study population was classified according to the T-score of bone mineral density at the femoral neck or total femur. A DL model for osteoporosis diagnosis was trained on the data sets and significant risk factors were investigated with local interpretable model-agnostic explanations (LIME). The performance of the DL model was compared with that of ML models and conventional clinical tools. Additionally, contribution ranking of risk factors and individualized explanation of feature contribution were examined.

resultsOur DL model showed area under the curve (AUC) values of 0.851 (95% CI 0.844-0.858) and 0.922 (95% CI 0.916-0.928) for the femoral neck and total femur bone mineral density, respectively, using the NHANES data set. The corresponding AUC values for the KNHANES data set were 0.827 (95% CI 0.821-0.833) and 0.912 (95% CI 0.898-0.927), respectively. Through the LIME method, significant features were induced, and each feature's integrated contribution and interpretation for individual risk were determined.

conclusionsThe developed DL model significantly outperforms conventional ML models and clinical tools. Our XAI model produces high-ranked features along with the integrated contributions of each feature, which facilitates the interpretation of individual risk. In summary, our interpretable model for osteoporosis risk screening outperformed state-of-the-art methods.

Indexed as

Deep LearningOsteoporosisArtificial IntelligenceCalcium CompoundsHumansNutrition SurveysOxidesCalcium CompoundslimeOxidesartificial intelligencedeep learningmachine learningosteoporosisrisk factorsscreening

Identifiers

PMID36482780
PMCPMC9883743

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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.