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AI prediction models with omics data utilization for atherosclerosis: A systematic scoping review and meta-analysis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Yunbeom | - |
| dc.contributor.author | Park, Kwanwoo | - |
| dc.contributor.author | Lee, Ji Hyun | - |
| dc.contributor.author | Lee, Sang-Hak | - |
| dc.date.accessioned | 2026-06-18T01:50:03Z | - |
| dc.date.available | 2026-06-18T01:50:03Z | - |
| dc.date.created | 2026-06-08 | - |
| dc.date.issued | 2026-05 | - |
| dc.identifier.issn | 0021-9150 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/212709 | - |
| dc.description.abstract | Background and aims Cardiovascular disease (CVD) remains a leading cause of global mortality, necessitating advanced methodologies to elucidate its complex pathophysiology. The application of artificial intelligence (AI) to interpret high-dimensional omics data offers a significant opportunity for precision medicine. This study aims to systematically review the current landscape of AI technologies in cardiovascular omics research and compare predictive performance of omics-trained AI prediction models (APMs) against conventional risk prediction models (CRMs) in atherosclerosis. Methods We employed a two-phase systematic review framework. Study 1 (scoping review) mapped the broad landscape of AI applications in cardiovascular omics research by reviewing 218 eligible studies. Study 2 (meta-analysis) comprised a systematic meta-analysis of 38 distinct, atherosclerosis-specific studies to quantify the incremental performance of APMs over CRMs, assessed via the difference in area under the curve (Delta AUC). Results Study 1 (scoping review) demonstrated substantial growth in AI modeling, multi-omics, and advanced omics methodologies from 2024 onwards. In Study 2 (meta-analysis), APMs significantly outperformed CRMs (pooled Delta AUC = 0.0586; 95% CI: 0.0335-0.0836; p < 0.0001) with a moderate level of between-study heterogeneity (I-2 = 40.02%, Cochran's Q test p = 0.0182). Conclusions Subsequent subgroup analyses revealed no significant moderator effects across differing experimental designs or validation strategies, indicating that the performance advantage of APMs remained robust across diverse analytical conditions. | - |
| dc.language | English | - |
| dc.publisher | Elsevier | - |
| dc.relation.isPartOf | ATHEROSCLEROSIS | - |
| dc.relation.isPartOf | ATHEROSCLEROSIS | - |
| dc.subject.MESH | Artificial Intelligence* | - |
| dc.subject.MESH | Atherosclerosis* / diagnosis | - |
| dc.subject.MESH | Atherosclerosis* / genetics | - |
| dc.subject.MESH | Atherosclerosis* / metabolism | - |
| dc.subject.MESH | Genomics* | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Predictive Value of Tests | - |
| dc.subject.MESH | Risk Assessment | - |
| dc.title | AI prediction models with omics data utilization for atherosclerosis: A systematic scoping review and meta-analysis | - |
| dc.type | Article | - |
| dc.contributor.googleauthor | Lee, Yunbeom | - |
| dc.contributor.googleauthor | Park, Kwanwoo | - |
| dc.contributor.googleauthor | Lee, Ji Hyun | - |
| dc.contributor.googleauthor | Lee, Sang-Hak | - |
| dc.identifier.doi | 10.1016/j.atherosclerosis.2026.120747 | - |
| dc.relation.journalcode | J00260 | - |
| dc.identifier.eissn | 1879-1484 | - |
| dc.identifier.pmid | 42008954 | - |
| dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0021915026001139 | - |
| dc.subject.keyword | Artificial intelligence | - |
| dc.subject.keyword | Omics | - |
| dc.subject.keyword | Risk prediction | - |
| dc.subject.keyword | Diagnosis model | - |
| dc.subject.keyword | Meta-analysis | - |
| dc.subject.keyword | Atherosclerosis | - |
| dc.subject.keyword | Precision medicine | - |
| dc.contributor.affiliatedAuthor | Lee, Sang-Hak | - |
| dc.identifier.scopusid | 2-s2.0-105036428237 | - |
| dc.identifier.wosid | 001752556100001 | - |
| dc.citation.volume | 416 | - |
| dc.identifier.bibliographicCitation | ATHEROSCLEROSIS, Vol.416, 2026-05 | - |
| dc.identifier.rimsid | 93273 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Artificial intelligence | - |
| dc.subject.keywordAuthor | Omics | - |
| dc.subject.keywordAuthor | Risk prediction | - |
| dc.subject.keywordAuthor | Diagnosis model | - |
| dc.subject.keywordAuthor | Meta-analysis | - |
| dc.subject.keywordAuthor | Atherosclerosis | - |
| dc.subject.keywordAuthor | Precision medicine | - |
| dc.subject.keywordPlus | CORONARY-HEART-DISEASE | - |
| dc.subject.keywordPlus | CARDIOVASCULAR-DISEASE | - |
| dc.subject.keywordPlus | RISK | - |
| dc.subject.keywordPlus | SCORE | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Cardiac & Cardiovascular Systems | - |
| dc.relation.journalWebOfScienceCategory | Peripheral Vascular Disease | - |
| dc.relation.journalResearchArea | Cardiovascular System & Cardiology | - |
| dc.identifier.articleno | 120747 | - |
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