Identification of iron metabolism-related genes in coronary heart disease and construction of a diagnostic model

被引:1
作者
Zhu, Lin [1 ]
Zhang, Jianxin [1 ]
Fan, Wenhui [1 ]
Su, Chen [1 ]
Jin, Zhi [1 ]
机构
[1] Shandong Univ, Hosp 2, Dept Tradit Chinese Med, Jinan, Peoples R China
来源
FRONTIERS IN CARDIOVASCULAR MEDICINE | 2024年 / 11卷
关键词
coronary heart disease; iron metabolism; diagnostic model; immune infiltration; WGCNA; ARTERY-DISEASE; T-CELLS; FERROPTOSIS; ATHEROSCLEROSIS; ASSOCIATION; MACROPHAGES; ANEMIA; ACTIVATION; EXPRESSION; LEVEL;
D O I
10.3389/fcvm.2024.1409605
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Coronary heart disease is a common cardiovascular disease, yferroptosiset its relationship with iron metabolism remains unclear.Methods Gene expression data from peripheral blood samples of patients with coronary heart disease and a healthy control group were utilized for a comprehensive analysis that included differential expression analysis, weighted gene co-expression network analysis, gene enrichment analysis, and the development of a logistic regression model to investigate the associations and differences between the groups. Additionally, the CIBERSORT algorithm was employed to examine the composition of immune cell types within the samples.Results Eight central genes were identified as being both differentially expressed and related to iron metabolism. These central genes are mainly involved in the cellular stress response. A logistic regression model based on the central genes achieved an AUC of 0.64-0.65 in the diagnosis of coronary heart disease. A higher proportion of M0 macrophages was found in patients with coronary heart disease, while a higher proportion of CD8T cells was observed in the normal control group.Conclusion The study identified important genes related to iron metabolism in the pathogenesis of coronary heart disease and constructed a robust diagnostic model. The results suggest that iron metabolism and immune cells may play a significant role in the development of coronary heart disease, providing a basis for further research.
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页数:12
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共 69 条
[1]   Monocyte and macrophage subtypes as paired cell biomarkers for coronary artery disease [J].
Arnold, Kathryn A. ;
Blair, John E. ;
Paul, Jonathan D. ;
Shah, Atman P. ;
Nathan, Sandeep ;
Alenghat, Francis J. .
EXPERIMENTAL PHYSIOLOGY, 2019, 104 (09) :1343-1352
[2]   Inhibition of ferroptosis alleviates atherosclerosis through attenuating lipid peroxidation and endothelial dysfunction in mouse aortic endothelial cell [J].
Bai, Tao ;
Li, Mingxing ;
Liu, Yuanfeng ;
Qiao, Zhentao ;
Wang, Zhiwei .
FREE RADICAL BIOLOGY AND MEDICINE, 2020, 160 :92-102
[3]   Macrophages in Atherosclerosis Regression [J].
Barrett, Tessa J. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2020, 40 (01) :20-33
[4]   Body iron stores had no impact on coronary heart disease outcomes: a middle-aged male cohort from the general population with 21-year follow-up [J].
Barywani, Salim Bary ;
Ostgard Thunstrom, Erik ;
Mandalenakis, Zacharias ;
Hansson, Per-Olof .
OPEN HEART, 2022, 9 (01)
[5]   ELAVL1 is transcriptionally activated by FOXC1 and promotes ferroptosis in myocardial ischemia/reperfusion injury by regulating autophagy [J].
Chen, Hui-Yong ;
Xiao, Ze-Zhou ;
Ling, Xiao ;
Xu, Rong-Ning ;
Zhu, Peng ;
Zheng, Shao-Yi .
MOLECULAR MEDICINE, 2021, 27 (01)
[6]   Identification and validation of ferroptosis-related genes and immune cell infiltration in thyroid associated ophthalmopathy [J].
Chen, Sainan ;
Diao, Jiale ;
Yue, Zifan ;
Wei, Ruili .
FRONTIERS IN GENETICS, 2023, 14
[7]   Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages [J].
Christofidou, Paraskevi ;
Nelson, Christopher P. ;
Nikpay, Majid ;
Qu, Liming ;
Li, Mingyao ;
Loley, Christina ;
Debiec, Radoslaw ;
Braund, Peter S. ;
Denniff, Matthew ;
Charchar, Fadi J. ;
Arjo, Ares Rocanin ;
Tregouet, David-Alexandre ;
Goodall, Alison H. ;
Cambien, Francois ;
Ouwehand, Willem H. ;
Roberts, Robert ;
Schunkert, Heribert ;
Hengstenberg, Christian ;
Reilly, Muredach P. ;
Erdmann, Jeanette ;
McPherson, Ruth ;
Koenig, Inke R. ;
Thompson, John R. ;
Samani, Nilesh J. ;
Tomaszewski, Maciej .
AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 97 (02) :228-237
[8]   Macrophage phenotypes in atherosclerosis [J].
Colin, Sophie ;
Chinetti-Gbaguidi, Giulia ;
Staels, Bart .
IMMUNOLOGICAL REVIEWS, 2014, 262 (01) :153-166
[9]   Iron status and its association with coronary heart disease: Systematic review and meta-analysis of prospective studies [J].
Das De, Sudeep ;
Krishna, Sreedhar ;
Jethwa, Ankeet .
ATHEROSCLEROSIS, 2015, 238 (02) :296-303
[10]   Circulating CD4+ CXCR5+ T cells contribute to proinflammatory responses in multiple ways in coronary artery disease [J].
Ding, Ru ;
Gao, Wenwu ;
He, Zhiqing ;
Wu, Feng ;
Chu, Yang ;
Wu, Jie ;
Ma, Lan ;
Liang, Chun .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2017, 52 :318-323