冠状动脉疾病
组学
计算机辅助设计
单核苷酸多态性
SNP公司
代谢组学
疾病
医学
生物信息学
内科学
队列
生物
计算生物学
肿瘤科
遗传学
基因
基因型
生物化学
作者
Paul Hsu,Chi-Hsiao Yeh,Chi-Jen Lo,Tsung-Hsien Tsai,Yun-Hsuan Chan,Yi-Ju Chou,Ning-I Yang,Mei‐Ling Cheng,Wayne Huey‐Herng Sheu,Chi‐Chun Lai,Huey‐Kang Sytwu,Ting‐Fen Tsai
标识
DOI:10.1186/s40364-025-00821-y
摘要
Abstract Background Coronary artery disease (CAD) remains a leading cause of mortality in developed nations. While previous genome-wide association studies have identified single-nucleotide polymorphisms (SNPs) linked to CAD, their impact on disease progression requires trans-omics validation. Methods This study merges whole genome SNP analysis and metabolomic profiling to distinguish CAD patients from high-risk and healthy individuals. A cross-sectional study was conducted, enrolling participants from the Northeastern Taiwan Community Medicine Research Cohort, which spans the period between August 2013 and November 2020. A total of 781 participants were included in the study and categorized into three groups: control ( n = 271), high-risk ( n = 363), and CAD ( n = 147) groups, following a stratification protocol. The study integrated K-clustering of metabolomics and SNP datasets. Subsequently, a machine-learning (ML)-assisted prediction model was developed specifically for CAD identification. Results Four significant findings emerged. Firstly, plasma levels of phospholipids decline from healthy controls to high-risk individuals and then decline further among CAD patients. This indicates that plasma phospholipids have potential as biomarkers and implies that they have a role in CAD progression. Secondly, five genes are linked to lipidomic alterations via their top-ranking among CAD-associated SNPs. Thirdly, a specific LPCAT1 haplotype is associated with CAD using a trans-omics approach. Lastly, an ML-assisted trans-omics prediction model for CAD was developed, which achieves an area under the curve of 0.917, with LPCAT1 among the 16 top-ranked predictive features. Conclusion This study highlights the usefulness of a multi-omics signature when discriminating CAD patients and suggests that abnormalities in phospholipid metabolism are influenced by LPCAT1 genetic variants. Our findings underscore the potential of multi-omics approaches to our understanding and identification of critical factors in CAD development. Trial registration number and date of registration ClinicalTrials.gov Identifier: NCT04839796; Aug 2013.
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