Alessandra Breschi, Yuliang Wang, Sarah Short, Wilman Luk, David Erani, Pouya Kheradpour, Peter Cimermancic, Gary J Tong, Jean Philippe Martin, Manway Liu, Lulu Cao, Daniel Liu, Ranee Chatterjee, Lydia Coulter Kwee, Thomas M Snyder, Andrew Han, Katherine Drake, Charles C Kim
{"title":"项目基线健康研究中与2型糖尿病相关的蛋白质组学测量的多模态分析","authors":"Alessandra Breschi, Yuliang Wang, Sarah Short, Wilman Luk, David Erani, Pouya Kheradpour, Peter Cimermancic, Gary J Tong, Jean Philippe Martin, Manway Liu, Lulu Cao, Daniel Liu, Ranee Chatterjee, Lydia Coulter Kwee, Thomas M Snyder, Andrew Han, Katherine Drake, Charles C Kim","doi":"10.1038/s43856-025-00964-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Understanding diabetes at the molecular level can help refine diagnostic approaches and personalized treatment efforts.</p><p><strong>Methods: </strong>We generated proteomic data from plasma collected from participants enrolled in the longitudinal observational cohort study Project Baseline Health Study (PBHS) (evaluated cohort, n = 738, 27.9% of the total PBHS cohort), and integrated those data with information from their medical history and laboratory tests to determine diabetes status. We then identified biomarker proteins associated with diabetes status.</p><p><strong>Results: </strong>Here we identify 87 differentially expressed proteins in people with diabetes compared to those without diabetes, 71 of which show higher expression. This proteomic profile, integrated with clinical data into a logistic regression model, can discriminate diabetes status with over 85% balanced accuracy.</p><p><strong>Conclusions: </strong>Our approach indicates that proteomic data can enhance diabetes phenotyping, showing potential for marker-based stratification of diabetes diagnosis. These results suggest that a holistic molecular-clinical approach to diagnosis might help personalize treatments or interventions for people with diabetes.</p>","PeriodicalId":72646,"journal":{"name":"Communications medicine","volume":"5 1","pages":"272"},"PeriodicalIF":5.4000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12222898/pdf/","citationCount":"0","resultStr":"{\"title\":\"Multi-modal analyses of proteomic measurements associated with type 2 diabetes from the Project Baseline Health Study.\",\"authors\":\"Alessandra Breschi, Yuliang Wang, Sarah Short, Wilman Luk, David Erani, Pouya Kheradpour, Peter Cimermancic, Gary J Tong, Jean Philippe Martin, Manway Liu, Lulu Cao, Daniel Liu, Ranee Chatterjee, Lydia Coulter Kwee, Thomas M Snyder, Andrew Han, Katherine Drake, Charles C Kim\",\"doi\":\"10.1038/s43856-025-00964-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Understanding diabetes at the molecular level can help refine diagnostic approaches and personalized treatment efforts.</p><p><strong>Methods: </strong>We generated proteomic data from plasma collected from participants enrolled in the longitudinal observational cohort study Project Baseline Health Study (PBHS) (evaluated cohort, n = 738, 27.9% of the total PBHS cohort), and integrated those data with information from their medical history and laboratory tests to determine diabetes status. We then identified biomarker proteins associated with diabetes status.</p><p><strong>Results: </strong>Here we identify 87 differentially expressed proteins in people with diabetes compared to those without diabetes, 71 of which show higher expression. This proteomic profile, integrated with clinical data into a logistic regression model, can discriminate diabetes status with over 85% balanced accuracy.</p><p><strong>Conclusions: </strong>Our approach indicates that proteomic data can enhance diabetes phenotyping, showing potential for marker-based stratification of diabetes diagnosis. These results suggest that a holistic molecular-clinical approach to diagnosis might help personalize treatments or interventions for people with diabetes.</p>\",\"PeriodicalId\":72646,\"journal\":{\"name\":\"Communications medicine\",\"volume\":\"5 1\",\"pages\":\"272\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12222898/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Communications medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1038/s43856-025-00964-x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s43856-025-00964-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Multi-modal analyses of proteomic measurements associated with type 2 diabetes from the Project Baseline Health Study.
Background: Understanding diabetes at the molecular level can help refine diagnostic approaches and personalized treatment efforts.
Methods: We generated proteomic data from plasma collected from participants enrolled in the longitudinal observational cohort study Project Baseline Health Study (PBHS) (evaluated cohort, n = 738, 27.9% of the total PBHS cohort), and integrated those data with information from their medical history and laboratory tests to determine diabetes status. We then identified biomarker proteins associated with diabetes status.
Results: Here we identify 87 differentially expressed proteins in people with diabetes compared to those without diabetes, 71 of which show higher expression. This proteomic profile, integrated with clinical data into a logistic regression model, can discriminate diabetes status with over 85% balanced accuracy.
Conclusions: Our approach indicates that proteomic data can enhance diabetes phenotyping, showing potential for marker-based stratification of diabetes diagnosis. These results suggest that a holistic molecular-clinical approach to diagnosis might help personalize treatments or interventions for people with diabetes.