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Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention

AIM: Reducing the high morbidity and mortality of ST-segment elevation myocardial infarction (STEMI) and improving patient prognosis remains a major global challenge. This study aimed to explore whether dynamic fluctuations in biomarkers are valuable predictors of prognosis in patients with STEMI. M...

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Autores principales: Liu, Yehong, Liu, Jie, Liu, Longqun, Cao, Shaoqing, Jin, Tianhui, Chen, Liang, Wu, Gangyong, Zong, Gangjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438435/
https://www.ncbi.nlm.nih.gov/pubmed/37600225
http://dx.doi.org/10.2147/JIR.S421491
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author Liu, Yehong
Liu, Jie
Liu, Longqun
Cao, Shaoqing
Jin, Tianhui
Chen, Liang
Wu, Gangyong
Zong, Gangjun
author_facet Liu, Yehong
Liu, Jie
Liu, Longqun
Cao, Shaoqing
Jin, Tianhui
Chen, Liang
Wu, Gangyong
Zong, Gangjun
author_sort Liu, Yehong
collection PubMed
description AIM: Reducing the high morbidity and mortality of ST-segment elevation myocardial infarction (STEMI) and improving patient prognosis remains a major global challenge. This study aimed to explore whether dynamic fluctuations in biomarkers are valuable predictors of prognosis in patients with STEMI. METHODS: This study included 216 patients with STEMI. Blood routine tests were performed on admission, 12 h after percutaneous coronary intervention (PCI), and at discharge. Systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), and pan-immune-inflammation-value (PIV) serum immune-inflammatory markers were calculated. The Cox proportional hazard model was used to assess the factors independently associated with the prognosis of STEMI. The optimal cutoff values for the inflammatory markers were calculated. RESULTS: Eighty-five (39.35%) of the 216 patients had major adverse cardiovascular events (MACEs) during the 1-year follow-up. Most were male (81.18%) with a median age of 64 years (interquartile, 55–69.5). Killip class ≥ II on admission (hazard ratio [HR], 1.859; 95% CI, 1.169–2.957; P = 0.009), total stent length (HR, 1.016; 95% CI, 1.003–1.029; P = 0.019), values of SIRI at 12 h after PCI (HR, 1.079; 95% CI, 1.050–1.108; P < 0.001), and the Gensini score (HR, 1.014; 95% CI, 1.007–1.022; P < 0.001) were independently associated with an increased risk of MACEs. Compared with SII, SIRI and PIV calculated at various time points and dynamically fluctuating changes, SIRI (cutoff value, 4.15; 95% CI, 0.701–0.819; P < 0.001) and PIV (cutoff value, 622.71; 95% CI, 0.674–0.796; P < 0.001) at 12 h after PCI showed the best efficacy for the prognosis of STEMI. CONCLUSION: Our study provides relevant evidence to the notion that SIRI or PIV at 12 h after PCI may be more accurate and economical predictors of long-term adverse prognosis in patients with STEMI.
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spelling pubmed-104384352023-08-19 Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention Liu, Yehong Liu, Jie Liu, Longqun Cao, Shaoqing Jin, Tianhui Chen, Liang Wu, Gangyong Zong, Gangjun J Inflamm Res Original Research AIM: Reducing the high morbidity and mortality of ST-segment elevation myocardial infarction (STEMI) and improving patient prognosis remains a major global challenge. This study aimed to explore whether dynamic fluctuations in biomarkers are valuable predictors of prognosis in patients with STEMI. METHODS: This study included 216 patients with STEMI. Blood routine tests were performed on admission, 12 h after percutaneous coronary intervention (PCI), and at discharge. Systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), and pan-immune-inflammation-value (PIV) serum immune-inflammatory markers were calculated. The Cox proportional hazard model was used to assess the factors independently associated with the prognosis of STEMI. The optimal cutoff values for the inflammatory markers were calculated. RESULTS: Eighty-five (39.35%) of the 216 patients had major adverse cardiovascular events (MACEs) during the 1-year follow-up. Most were male (81.18%) with a median age of 64 years (interquartile, 55–69.5). Killip class ≥ II on admission (hazard ratio [HR], 1.859; 95% CI, 1.169–2.957; P = 0.009), total stent length (HR, 1.016; 95% CI, 1.003–1.029; P = 0.019), values of SIRI at 12 h after PCI (HR, 1.079; 95% CI, 1.050–1.108; P < 0.001), and the Gensini score (HR, 1.014; 95% CI, 1.007–1.022; P < 0.001) were independently associated with an increased risk of MACEs. Compared with SII, SIRI and PIV calculated at various time points and dynamically fluctuating changes, SIRI (cutoff value, 4.15; 95% CI, 0.701–0.819; P < 0.001) and PIV (cutoff value, 622.71; 95% CI, 0.674–0.796; P < 0.001) at 12 h after PCI showed the best efficacy for the prognosis of STEMI. CONCLUSION: Our study provides relevant evidence to the notion that SIRI or PIV at 12 h after PCI may be more accurate and economical predictors of long-term adverse prognosis in patients with STEMI. Dove 2023-08-14 /pmc/articles/PMC10438435/ /pubmed/37600225 http://dx.doi.org/10.2147/JIR.S421491 Text en © 2023 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liu, Yehong
Liu, Jie
Liu, Longqun
Cao, Shaoqing
Jin, Tianhui
Chen, Liang
Wu, Gangyong
Zong, Gangjun
Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention
title Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention
title_full Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention
title_fullStr Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention
title_full_unstemmed Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention
title_short Association of Systemic Inflammatory Response Index and Pan-Immune-Inflammation-Value with Long-Term Adverse Cardiovascular Events in ST-Segment Elevation Myocardial Infarction Patients After Primary Percutaneous Coronary Intervention
title_sort association of systemic inflammatory response index and pan-immune-inflammation-value with long-term adverse cardiovascular events in st-segment elevation myocardial infarction patients after primary percutaneous coronary intervention
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438435/
https://www.ncbi.nlm.nih.gov/pubmed/37600225
http://dx.doi.org/10.2147/JIR.S421491
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