The progression of non-culprit coronary lesion is related to higher SII, SIRI, and PIV in patients with ACS

被引:0
作者
Zhou, Yilu [1 ]
Wang, Zhanglong [1 ]
Huang, Fanke [1 ]
Guan, Jing [1 ]
Wang, Yue [1 ]
Chen, Yuwen [1 ]
Li, Bingqing [1 ]
Lv, Jianfeng [1 ,2 ]
机构
[1] China Three Gorges Univ, Med Coll, Yichang, Hubei, Peoples R China
[2] Three Gorges Univ, Renhe Hosp, Dept Cardiol, Yichang 443000, Hubei, Peoples R China
关键词
acute coronary syndrome; non-culprit coronary lesion; pan-immune-inflammation value; percutaneous coronary intervention; progression; system inflammation response index; systemic immune inflammation index; MYOCARDIAL-INFARCTION; INTERVENTION; ASSOCIATION; PLATELETS; DISEASES;
D O I
10.1097/MD.0000000000041094
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coronary heart disease pathogenesis is intricately linked to inflammation. Acute coronary syndrome (ACS) is a coronary heart disease that seriously affects the prognosis of patients. New immune-inflammatory indices such as systemic immune inflammation index (SII), system inflammation response index (SIRI), and pan-immune-inflammation value (PIV) have emerged as potential biomarkers, offering reflection into systemic inflammatory states and assisting in the prognosis of diverse diseases. This research explored the association between the new immune-inflammatory indices (SII, SIRI, and PIV) and the progression of non-culprit coronary lesions (NCL) in patients with ACS after percutaneous coronary intervention (PCI). Our study investigated the potential association between the immune-inflammatory index (SII, SIRI, and PIV) and NCL progression in patients with ACS following PCI. We conducted a retrospective analysis of patients with ACS who underwent PCI twice at a single-center from 2019 to 2023. Clinical and angiographic features were collected from electronic medical records. The primary outcome was NCL progression. All patients were divided into a progression group and a non-progression group based on angiographies. The clinical and angiographic features were analyzed. The study included 311 ACS patients (progression group: 97 males, 34 females; non-progression group: male 146 males, 34 females). The SII, SIRI, and PIV were significantly higher in the NCL progression group than in the non-progression group (P < .001). Logistic regression analysis showed that SII, SIRI, and PIV were independent risk factors for the NCL progression and positively correlated with it (OR: 1.002, P < .001; OR: 2.188, P < .001; OR: 1.003, P < .001). ROC showed that the SII value was the highest in terms of sensitivity with a value of 67.18% (AUC = 0.7288, P < .001), and the SIRI was the highest in terms of specificity with a value of 79.44% (AUC = 0.6974, P < .001). The SII, SIRI, and PIV are valuable predictors of NCL progression in patients with ACS. Higher SII, SIRI, and PIV are related to the progression of NCL.
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页数:8
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  • [21] Pathophysiology of coronary artery disease[J]. Libby, P;Theroux, P. CIRCULATION, 2005(25)
  • [22] Mehta SR, 2019, NEW ENGL J MED, V381, P1411, DOI [10.1056/NEJMoa1907775, 10.1056/NEJMc2000278]
  • [23] Inflammatory Cells in Atherosclerosis[J]. Mehu, Marcelle;Narasimhulu, Chandrakala Aluganti;Singla, Dinender K. ANTIOXIDANTS, 2022(02)
  • [24] Association between chronic immune-mediated inflammatory diseases and cardiovascular risk[J]. Miguel Baena-Diez, Jose;Garcia-Gil, Maria;Comas-Cufi, Marc;Ramos, Rafel;Prieto-Alhambra, Daniel;Salvador-Gonzalez, Betlem;Elosua, Roberto;Degano, Irene R.;Penafiel, Judith;Grau, Maria. HEART, 2018(02)
  • [25] Platelets, inflammation and anti-inflammatory effects of antiplatelet drugs in ACS and CAD[J]. Mueller, Karin A. L.;Chatterjee, Madhumita;Rath, Dominik;Geisler, Tobias. THROMBOSIS AND HAEMOSTASIS, 2015(03)
  • [26] Comparison of pan-immune-inflammation value with other inflammation markers of long-term survival after ST-segment elevation myocardial infarction[J]. Murat, Bektas;Murat, Selda;Ozgeyik, Mehmet;Bilgin, Muzaffer. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2023(01)
  • [27] Predictive Factors and Impact of No Reflow After Primary Percutaneous Coronary Intervention in Patients With Acute Myocardial Infarction[J]. Ndrepepa, Gjin;Tiroch, Klaus;Keta, Dritan;Fusaro, Massimiliano;Seyfarth, Melchior;Pache, Juergen;Mehilli, Julinda;Schoemig, Albert;Kastrati, Adnan. CIRCULATION-CARDIOVASCULAR INTERVENTIONS, 2010(01)
  • [28] Coronary angiographic scoring systems: An evaluation of their equivalence and validity[J]. Neeland, Ian J.;Patel, Riyaz S.;Eshtehardi, Parham;Dhawan, Saurabh;McDaniel, Michael C.;Rab, S. Tanveer;Vaccarino, Viola;Zafari, A. Maziar;Samady, Habib;Quyyumi, Arshed A. AMERICAN HEART JOURNAL, 2012(04)
  • [29] Low Lymphocyte Count and Cardiovascular Diseases[J]. Nunez, J.;Minana, G.;Bodi, V.;Nunez, E.;Sanchis, J.;Husser, O.;Llacer, A. CURRENT MEDICINAL CHEMISTRY, 2011(21)
  • [30] Therapeutic implications of low lymphocyte count in non-ST segment elevation acute coronary syndromes[J]. Nunez, Julio;Sanchis, Juan;Bodi, Vicent;Nunez, Eduardo;Heatta, Anne M.;Minana, Gema;Merlos, Pilar;Rumiz, Eva;Palau, Patricia;Sanjuan, Rafael;Blasco, Maria L.;Llacer, Angel. EUROPEAN JOURNAL OF INTERNAL MEDICINE, 2009(08)