Evidence map›Paper›PMID 41225328›Full record

ArticleBMC cardiovascular disorders2025

Exploring the impact of pan-immune-inflammation-value and other traditional inflammation-based markers on coronary collateral circulation in patients with chronic total occlusion.

Kenan Toprak, Mesut Karataş

Abstract readComparative Study
In one paragraph

Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Kenan ToprakFaculty of Medicine, Department of Cardiology, Harran University, Viranşehir road, Sanliurfa, 63000, Turkey. kentoprak@hotmail.com.
Mesut KarataşDepartment of Cardiology, Kartal Kosuyolu High Specialization Training and Research Hospital, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary collateral circulation (CCC) plays a pivotal role in mitigating the adverse effects of chronic total occlusion (CTO) by providing an alternative blood supply to ischemic myocardium. In recent years, there has been a growing interest in understanding the relationship between inflammation and coronary collateral development. However, the predictive role of pan immune inflammation value (PIV), a new and expanded inflammatory response marker, on CCC has not yet been investigated. This article aims to provide a detailed comparison of the effect of PIV and other traditional inflammation-based markers on CCC in patients with CTO.

methods467 patients who underwent coronary angiography due to non-ST elevation myocardial infarction (NSTEMI) and were detected to have CTO in epicardial coronary artery were included in the study. The patients were divided into two groups as poor CCC and good CCC according to the Rentrop classification, and the inflammation-based marker values of the groups were compared.

resultsThe PIV values of NSTEMI patients were significantly higher in the poor CCC group than those in the good CCC group. High PIV values were determined as independent predictors for poor CCC (OR: 0.832, CI: 0.791-0.876, p < 0.001). With a 79% sensitivity and 78% specificity at the optimal cut-off value of 628.8, PIV demonstrated good predictive ability for identifying poor CCC (AUC: 0.785, CI: 0.744-0.826, p < 0.001).

conclusionPIV was found to be superior to traditional inflammation-based markers in discriminating pooc CCC in NSTEMI patients.

Indexed as

Collateral CirculationCoronary CirculationCoronary OcclusionInflammationInflammation MediatorsNon-ST Elevated Myocardial InfarctionAgedBiomarkersChronic DiseaseCoronary AngiographyFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisBiomarkersInflammation MediatorsChronic total occlusionCoronary collateral circulationInflammation-based markersNon-ST segment elevation myocardial infarctionPan-immune-inflammation value

Identifiers

PMID41225328
PMCPMC12613433

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