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全免疫炎症值和全身免疫炎症指数对识别冠状动脉易损斑块的预测价值:急性冠状动脉综合征患者光学相干断层扫描的新见解

Predictive Value of Pan-Immune Inflammation Value and Systemic Immune-Inflammation Index for Identifying Coronary Vulnerable Plaques: New Insights from Optical Coherence Tomography in Acute Coronary Syndrome Patients.

作者信息

Ji Jinrui, Wei Xiaoyun, Xue Bin, Wan Dongyu, Wu Lei, Liu Hengliang

机构信息

Clinical Medical Department, Faculty of Medicine, Henan University of Traditional Chinese Medicine, Zhengzhou, 450000, People's Republic of China.

Department of Cardiology, People's Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, 450000, People's Republic of China.

出版信息

J Inflamm Res. 2024 Dec 4;17:10371-10382. doi: 10.2147/JIR.S498292. eCollection 2024.

DOI:10.2147/JIR.S498292
PMID:39649422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11625432/
Abstract

PURPOSE

The predictive value of PIV and SII in identifying vulnerable plaques among ACS patients remains poorly understood. This study represents the inaugural use of OCT to identify vulnerable plaques and establishes a predictive model incorporating PIV and SII, enhancing clinical treatment strategies.

METHODS

A total of 523 eligible ACS patients underwent coronary angiography and OCT. Clinical data were collected and analyzed. Multifactorial logistic regression was employed to identify factors influencing TCFA. Receiver operating characteristic (ROC) curves were constructed to assess the diagnostic accuracy of the PIV and SII for TCFA, with a calculation of the area under the ROC curve (AUC). The optimal cutoff values for PVI and SII were calculated.

RESULTS

Compared to the non-TCFA group, the TCFA group exhibited significantly higher levels of hypersensitive C-reactive protein (hs-CRP), PIV, and SII (all P <0.05). Multifactorial logistic regression analysis revealed that PIV (odds ratio [OR], 1.78; 95% confidence interval [CI], 1.35-2.06; P <0.001) and SII (OR, 1.52; 95% CI, 1.14-2.08; P <0.001) were independent risk factors for TCFA development. The optimal cutoff value for PIV was 490.7, achieving a diagnostic sensitivity and specificity of 75.44% and 89.32%, respectively. For SII, the optimal cutoff value was 802.9, with a diagnostic sensitivity and specificity of 67.54% and 79.61%, respectively.

CONCLUSION

This study suggests that PIV and SII can serve as noninvasive, practical, and cost-effective biomarkers for evaluating plaque vulnerability in patients with ACS.

摘要

目的

外周炎症血管评分(PIV)和全身免疫炎症指标(SII)在识别急性冠状动脉综合征(ACS)患者易损斑块方面的预测价值仍知之甚少。本研究首次使用光学相干断层扫描(OCT)来识别易损斑块,并建立了一个包含PIV和SII的预测模型,以优化临床治疗策略。

方法

共有523例符合条件的ACS患者接受了冠状动脉造影和OCT检查。收集并分析临床数据。采用多因素逻辑回归分析确定影响薄帽纤维粥样斑块(TCFA)的因素。绘制受试者工作特征(ROC)曲线,评估PIV和SII对TCFA的诊断准确性,并计算ROC曲线下面积(AUC)。计算PIV和SII的最佳截断值。

结果

与非TCFA组相比,TCFA组的超敏C反应蛋白(hs-CRP)、PIV和SII水平显著更高(均P<0.05)。多因素逻辑回归分析显示,PIV(比值比[OR],1.78;95%置信区间[CI],1.35-2.06;P<0.001)和SII(OR,1.52;95%CI,1.14-2.08;P<0.001)是TCFA发生的独立危险因素。PIV的最佳截断值为490.7,诊断敏感性和特异性分别为75.44%和89.32%。对于SII,最佳截断值为802.9,诊断敏感性和特异性分别为67.54%和79.61%。

结论

本研究表明,PIV和SII可作为评估ACS患者斑块易损性的无创、实用且经济有效的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/47dc347c3b73/JIR-17-10371-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/2763d82ebef4/JIR-17-10371-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/bd75c501c3d5/JIR-17-10371-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/da03773b1dd0/JIR-17-10371-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/d8a64aab066f/JIR-17-10371-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/9143e6d39e14/JIR-17-10371-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/47dc347c3b73/JIR-17-10371-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/2763d82ebef4/JIR-17-10371-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/bd75c501c3d5/JIR-17-10371-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/da03773b1dd0/JIR-17-10371-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/d8a64aab066f/JIR-17-10371-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/9143e6d39e14/JIR-17-10371-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b52/11625432/47dc347c3b73/JIR-17-10371-g0006.jpg

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