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已发表论文

CRTP5 和 SII 对非 ST 段抬高型急性冠脉综合征患者冠状动脉严重程度及心肌纤维化的预测潜力:一项探索性生物标志物研究

 

Authors Ji J, Qiao M, Ding Y, Wei X, Wan D, Wu L, Liu H

Received 22 December 2024

Accepted for publication 28 May 2025

Published 3 June 2025 Volume 2025:18 Pages 7127—7138

DOI http://doi.org/10.2147/JIR.S513574

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Rongxue Wu

Jinrui Ji,1,2,* Mu Qiao,3,4,* Ya’nan Ding,1,2,* Xiaoyun Wei,1,2,* Dongyu Wan,1,2,* Lei Wu,1,2,* Hengliang Liu1,2,* 

1Clinical Medical Department, Faculty of Medicine, Henan University of Traditional Chinese Medicine, Zhengzhou, 450000, People’s Republic of China; 2Department of Cardiology, People’s Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, 450000, People’s Republic of China; 3Department of Cardiology, Seventh People’s Hospital of Zhengzhou, Zhengzhou, 450000, People’s Republic of China; 4Department of Cardiology, Zhengzhou Cardiovascular Institute, Zhengzhou, 450000, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Hengliang Liu, Department of Cardiology, People’s Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, 450000, People’s Republic of China, Email hnzzjjr@163.com

Purpose: Findings from this research aim to enhance clinical assessments of coronary artery disease severity and myocardial fibrosis (MF).
Methods: A total of 523 eligible non-ST-segment elevation acute coronary syndromes (NSTE-ACS) patients were included. Clinical data were collected and analyzed. Multifactorial logistic regression analysis was applied to identify factors influencing coronary artery lesions in patients with NSTE-ACS. Diagnostic accuracy for Complement C1q tumor necrosis factor-related protein 5 (CTRP5) and systemic immune-inflammation index (SII) in assessing coronary artery lesions and MF was analyzed via receiver operating characteristic (ROC) curve analysis.
Results: The levels of CTRP5 and SII were significantly different between the unstable angina pectoris (UAP) and ST-segment elevation myocardial infarction (NSTEMI) groups (all P< 0.05). Significant differences in CTRP5, SII, PCI, and PCIII were noted across the Single-, Two-, and Three-vessel lesion groups (all P< 0.05). Multifactorial logistic regression analysis revealed that CTRP5 (odds ratio [OR], 1.621; 95% confidence interval [CI], 1.103– 1.984; P< 0.001) and SII (OR, 1.473; 95% CI, 1.178– 1.840; P< 0.001) were independent risk factors for three-vessel lesions. The ROC curve analysis demonstrated that CTRP5 and SII effectively predicted three-vessel lesions, with area under curve (AUC) values of 0.823 [cut-off value13.99; 95% confidence interval (CI), 0.779– 0.866, P< 0.001] and 0.796 [cut-off value, 837.5; 95% CI, 0.747– 0.845, P< 0.001], respectively. The ROC curve analysis evaluated the ability of CTRP5 and SII to predict MF; AUC values were 0.809 (cut-off value, 11.95; 95% CI, 0.724– 0.895, P< 0.001) and 0.713 (cut-off value, 624.2; 95% CI, 0.611– 0.815, P< 0.001), respectively.
Conclusion: CTRP5 and SII demonstrate strong potential as early diagnostic markers for assessing the severity of coronary artery disease and MF in patients with NSTE-ACS.

Keywords: complement C1q tumor necrosis factor-related protein 5, systemic immune-inflammation index, myocardial fibrosis, non-ST-segment elevation acute coronary syndromes

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