Precision subclassification of type 2 diabetes: a systematic review
Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible resul...
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Published in | Communications medicine Vol. 3; no. 1; pp. 138 - 19 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Springer Nature B.V
05.10.2023
Nature Publishing Group UK Nature Portfolio |
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Online Access | Get full text |
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Abstract | Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients.
We searched PubMed and Embase for publications that used 'simple subclassification' approaches using simple categorisation of clinical characteristics, or 'complex subclassification' approaches which used machine learning or 'omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches.
Here we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes.
Critical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes. |
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AbstractList | Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients.
We searched PubMed and Embase for publications that used 'simple subclassification' approaches using simple categorisation of clinical characteristics, or 'complex subclassification' approaches which used machine learning or 'omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches.
Here we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes.
Critical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes. Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients.BACKGROUNDHeterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients.We searched PubMed and Embase for publications that used 'simple subclassification' approaches using simple categorisation of clinical characteristics, or 'complex subclassification' approaches which used machine learning or 'omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches.METHODSWe searched PubMed and Embase for publications that used 'simple subclassification' approaches using simple categorisation of clinical characteristics, or 'complex subclassification' approaches which used machine learning or 'omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches.Here we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes.RESULTSHere we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes.Critical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes.CONCLUSIONCritical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes. In people with type 2 diabetes there may be differences in the way people present, including for example, their symptoms, body weight or how much insulin they make. We looked at recent publications describing research in this area to see whether it is possible to separate people with type 2 diabetes into different subgroups and, if so, whether these groupings were useful for patients. We found that it is possible to group people with type 2 diabetes into different subgroups and being in one subgroup can be more strongly linked to the likelihood of developing complications over others. This might mean that in the future we can treat people in different subgroups differently in ways that improves their treatment and their health but it requires further study. Misra, Wagner et al. systematically review if strategies to subclassify type 2 diabetes (T2D) are associated with high quality evidence and patient outcomes. Cluster-based stratification yields T2D subtypes that associate with outcomes, suggesting subclassification could have future clinical use. BackgroundHeterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients.MethodsWe searched PubMed and Embase for publications that used ‘simple subclassification’ approaches using simple categorisation of clinical characteristics, or ‘complex subclassification’ approaches which used machine learning or ‘omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches.ResultsHere we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes.ConclusionCritical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes.Plain language summaryIn people with type 2 diabetes there may be differences in the way people present, including for example, their symptoms, body weight or how much insulin they make. We looked at recent publications describing research in this area to see whether it is possible to separate people with type 2 diabetes into different subgroups and, if so, whether these groupings were useful for patients. We found that it is possible to group people with type 2 diabetes into different subgroups and being in one subgroup can be more strongly linked to the likelihood of developing complications over others. This might mean that in the future we can treat people in different subgroups differently in ways that improves their treatment and their health but it requires further study. Abstract Background Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients. Methods We searched PubMed and Embase for publications that used ‘simple subclassification’ approaches using simple categorisation of clinical characteristics, or ‘complex subclassification’ approaches which used machine learning or ‘omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches. Results Here we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes. Conclusion Critical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes. Abstract Background Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a systematic review to determine whether strategies to subclassify type 2 diabetes were associated with high quality evidence, reproducible results and improved outcomes for patients. Methods We searched PubMed and Embase for publications that used ‘simple subclassification’ approaches using simple categorisation of clinical characteristics, or ‘complex subclassification’ approaches which used machine learning or ‘omics approaches in people with established type 2 diabetes. We excluded other diabetes subtypes and those predicting incident type 2 diabetes. We assessed quality, reproducibility and clinical relevance of extracted full-text articles and qualitatively synthesised a summary of subclassification approaches. Results Here we show data from 51 studies that demonstrate many simple stratification approaches, but none have been replicated and many are not associated with meaningful clinical outcomes. Complex stratification was reviewed in 62 studies and produced reproducible subtypes of type 2 diabetes that are associated with outcomes. Both approaches require a higher grade of evidence but support the premise that type 2 diabetes can be subclassified into clinically meaningful subtypes. Conclusion Critical next steps toward clinical implementation are to test whether subtypes exist in more diverse ancestries and whether tailoring interventions to subtypes will improve outcomes. |
ArticleNumber | 138 |
Author | Ozkan, Bige Schön, Martin Thuesen, Anne Cathrine Baun Eckel, Robert H Misra, Shivani Deutsch, Aaron J Kreienkamp, Raymond J Udler, Miriam S Duan, Daisy Goodarzi, Mark O Billings, Liana K Wallace, Amelia S Andersen, Mette K Sheu, Wayne Huey-Herng Meigs, James B Selvin, Elizabeth Ray, Debashree Prystupa, Katsiaryna Stefan, Norbert Sevilla-Gonzalez, Magdalena Leong, Aaron Hansen, Torben Rooney, Mary R Wang, Caroline C Florez, Jose C Wagner, Robert Cromer, Sara J |
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Magdalena orcidid: 0000-0001-6135-9998 surname: Sevilla-Gonzalez fullname: Sevilla-Gonzalez, Magdalena organization: Department of Medicine, Harvard Medical School, Boston, MA, USA – sequence: 6 givenname: Katsiaryna orcidid: 0000-0003-3368-1028 surname: Prystupa fullname: Prystupa, Katsiaryna organization: German Center for Diabetes Research (DZD), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany – sequence: 7 givenname: Caroline C surname: Wang fullname: Wang, Caroline C organization: Welch Center for Prevention, Epidemiology, and Clinical Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA – sequence: 8 givenname: Raymond J orcidid: 0000-0002-1683-323X surname: Kreienkamp fullname: Kreienkamp, Raymond J organization: Department of Pediatrics, Division of Endocrinology, Boston Children's Hospital, Boston, MA, USA – sequence: 9 givenname: Sara J surname: Cromer fullname: Cromer, Sara J organization: Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA – sequence: 10 givenname: Mary R orcidid: 0000-0002-5607-4848 surname: Rooney fullname: Rooney, Mary R organization: Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA – sequence: 11 givenname: Daisy orcidid: 0000-0002-4392-3206 surname: Duan fullname: Duan, Daisy organization: Division of Endocrinology, Diabetes and Metabolism, Johns Hopkins University School of Medicine, Baltimore, MD, USA – sequence: 12 givenname: Anne Cathrine Baun orcidid: 0000-0002-8639-9117 surname: Thuesen fullname: Thuesen, Anne Cathrine Baun organization: Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark – sequence: 13 givenname: Amelia S orcidid: 0000-0002-1466-3791 surname: Wallace fullname: Wallace, Amelia S organization: Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA – sequence: 14 givenname: 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University of Colorado School of Medicine, Aurora, CO, USA – sequence: 19 givenname: Wayne Huey-Herng surname: Sheu fullname: Sheu, Wayne Huey-Herng organization: Division of Endocrinology and Metabolism, Taipei Veterans General Hospital, Taipei, Taiwan, ROC – sequence: 20 givenname: Torben orcidid: 0000-0001-8748-3831 surname: Hansen fullname: Hansen, Torben organization: Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark – sequence: 21 givenname: Norbert orcidid: 0000-0002-2186-9595 surname: Stefan fullname: Stefan, Norbert organization: Institute of Diabetes Research and Metabolic Diseases (IDM), Helmholtz Center Munich, Neuherberg, Germany – sequence: 22 givenname: Mark O orcidid: 0000-0001-6364-5103 surname: Goodarzi fullname: Goodarzi, Mark O organization: Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA – 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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37798471$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Contributor | Steenackers, Nele Mekonnen, Eskedar Getie Stanislawski, Maggie A Semnani-Azad, Zhila de Souza, Russell Clark, Amy L Laffel, Lori M Hughes, Alice Vesco, Kimberly K Deutsch, Aaron J Wentworth, John M Sherifali, Diana Ikle, Jennifer M Pilla, Scott J Kreienkamp, Raymond J Pop-Busui, Rodica Clemmensen, Christoffer Miller, Rachel G Jacobsen, Laura M Urazbayeva, Marzhan Tosur, Mustafa Brown, Rebecca J Aukrust, Ingvild Saeed, Zeb Griffin, Kurt Hattersley, Andrew T Liu, Kai Hirsch, Irl B Sims, Emily K Leong, Aaron Owen, Katharine R Redondo, Maria J Zhang, Cuilin Dennis, John M Massey, Robert Gitelman, Stephen E Steck, Andrea K Ukke, Gebresilasea Gendisha Koivula, Robert W Corcoy, Rosa Fitipaldi, Hugo Huang, Chuiguo Vatier, Camille Ozkan, Bige Schön, Martin Monaco, Gabriela S F Yamamoto, Jennifer M Petrie, John R Molnes, Janne Takele, Wubet Worku Chen, Mingling Chivers, Sian C Naylor, Rochelle N Loos, Ruth J F Kettunen, Jarno L T Gingras, Véronique Lowe, Jr, William L Beltrand, Jacques Leung, Gloria K W Udler, Miriam S Goodarzi, Mark O Hannah, Wesley Zhang |
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Snippet | Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We undertook a... Abstract Background Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical... BackgroundHeterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical outcomes. We... In people with type 2 diabetes there may be differences in the way people present, including for example, their symptoms, body weight or how much insulin they... Abstract Background Heterogeneity in type 2 diabetes presentation and progression suggests that precision medicine interventions could improve clinical... |
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SubjectTerms | Biomarkers Body mass index Diabetes Glucose Machine learning Pathophysiology Precision medicine Systematic review Urine |
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Title | Precision subclassification of type 2 diabetes: a systematic review |
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