Bo Liu, Xiangzhou Zhang, Kang Liu, Xinhou Hu, Eric W T Ngai, Weiqi Chen, Ho Yin Chan, Yong Hu, Mei Liu
{"title":"基于子群学习的可解释建模框架:糖尿病肾病预测研究。","authors":"Bo Liu, Xiangzhou Zhang, Kang Liu, Xinhou Hu, Eric W T Ngai, Weiqi Chen, Ho Yin Chan, Yong Hu, Mei Liu","doi":"10.1177/14604582241291379","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Complex diseases, like diabetic kidney disease (DKD), often exhibit heterogeneity, challenging accurate risk prediction with machine learning. Traditional global models ignore patient differences, and subgroup learning lacks interpretability and predictive efficiency. This study introduces the Interpretable Subgroup Learning-based Modeling (iSLIM) framework to address these issues.</p><p><strong>Methods: </strong>iSLIM integrates expert knowledge with a tree-based recursive partitioning approach to identify DKD subgroups within an EHR dataset of 11,559 patients. It then constructs separate models for each subgroup, enhancing predictive accuracy while preserving interpretability.</p><p><strong>Results: </strong>Five clinically relevant subgroups are identified, achieving an average sensitivity of 0.8074, outperforming a single global model by 0.1104. Post hoc analyses provide pathological and biological evidence supporting subgroup validity and potential DKD risk factors.</p><p><strong>Conclusion: </strong>The iSLIM surpasses traditional global model in predictive performance and subgroup-specific risk factor interpretation, enhancing the understanding of DKD's heterogeneous mechanisms and potentially increasing the adoption of machine learning models in clinical decision-making.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interpretable subgroup learning-based modeling framework: Study of diabetic kidney disease prediction.\",\"authors\":\"Bo Liu, Xiangzhou Zhang, Kang Liu, Xinhou Hu, Eric W T Ngai, Weiqi Chen, Ho Yin Chan, Yong Hu, Mei Liu\",\"doi\":\"10.1177/14604582241291379\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Complex diseases, like diabetic kidney disease (DKD), often exhibit heterogeneity, challenging accurate risk prediction with machine learning. Traditional global models ignore patient differences, and subgroup learning lacks interpretability and predictive efficiency. This study introduces the Interpretable Subgroup Learning-based Modeling (iSLIM) framework to address these issues.</p><p><strong>Methods: </strong>iSLIM integrates expert knowledge with a tree-based recursive partitioning approach to identify DKD subgroups within an EHR dataset of 11,559 patients. It then constructs separate models for each subgroup, enhancing predictive accuracy while preserving interpretability.</p><p><strong>Results: </strong>Five clinically relevant subgroups are identified, achieving an average sensitivity of 0.8074, outperforming a single global model by 0.1104. Post hoc analyses provide pathological and biological evidence supporting subgroup validity and potential DKD risk factors.</p><p><strong>Conclusion: </strong>The iSLIM surpasses traditional global model in predictive performance and subgroup-specific risk factor interpretation, enhancing the understanding of DKD's heterogeneous mechanisms and potentially increasing the adoption of machine learning models in clinical decision-making.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/14604582241291379\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/14604582241291379","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Interpretable subgroup learning-based modeling framework: Study of diabetic kidney disease prediction.
Objectives: Complex diseases, like diabetic kidney disease (DKD), often exhibit heterogeneity, challenging accurate risk prediction with machine learning. Traditional global models ignore patient differences, and subgroup learning lacks interpretability and predictive efficiency. This study introduces the Interpretable Subgroup Learning-based Modeling (iSLIM) framework to address these issues.
Methods: iSLIM integrates expert knowledge with a tree-based recursive partitioning approach to identify DKD subgroups within an EHR dataset of 11,559 patients. It then constructs separate models for each subgroup, enhancing predictive accuracy while preserving interpretability.
Results: Five clinically relevant subgroups are identified, achieving an average sensitivity of 0.8074, outperforming a single global model by 0.1104. Post hoc analyses provide pathological and biological evidence supporting subgroup validity and potential DKD risk factors.
Conclusion: The iSLIM surpasses traditional global model in predictive performance and subgroup-specific risk factor interpretation, enhancing the understanding of DKD's heterogeneous mechanisms and potentially increasing the adoption of machine learning models in clinical decision-making.