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      Advanced Lung Cancer Inflammation Index for Predicting Prognostic Risk for Patients with Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention

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          Abstract

          Purpose

          The decreased advanced lung cancer inflammation index (ALI), defined as body mass index (BMI) * albumin (Alb)/neutrophil-to-lymphocyte ratio (NLR), is an independent prognostic risk factor for overall survival in gastric, lung, and colorectal cancers. This study aimed to investigate the value of ALI in predicting the risk of major adverse cardiovascular events (MACEs) in patients with acute coronary syndrome (ACS).

          Patients and Methods

          A total of 1624 patients with ACS undergoing percutaneous coronary intervention (PCI) were consecutively enrolled between January 2016 and December 2018. Follow-up data were collected at 1, 3, 6, and 12 months and annually thereafter. The primary endpoints were MACEs. All endpoints were defined as all-cause mortality, recurrent angina pectoris, restenosis/intra stent thrombosis, stroke, heart failure, and all-cause bleeding.

          Results

          The MACEs group and non-MACEs group showed significant differences in patients with age >65 years (28 [50.0%] vs 319 [23.7%]), history of heart failure (16 [28.6%] vs 127 [9.4%]), history of ischemic stroke (14 [25.0%] vs 186 [13.8%]), history of cardiogenic shock (6 [10.71%] vs 16 [1.19%]), left ventricular ejection fraction <40% (8 [14.29%] vs 33 [2.46%]), and ALI <343.96 (44 [78.65%] vs 680 [50.60%]) (all p<0.001). The optimal cut-off value for ALI was 334.96. The area under the curve (AUC) of the 1-, 2-, 3-, and 5-year was 0.560, 0.577, 0.665, and 0.749, respectively. The survival rate was significantly lower in the low ALI group than in the high ALI group (log-rank p<0.001). Low ALI was an independent risk factor for the long-term prognosis of patients with ACS after PCI, univariate HR: 3.671, 95% CI: 1.938–6.953, p<0.001; multivariate HR: 3.009, 95% CI: 1.57–5.769, p=0.001.

          Conclusion

          ALI score less than 334.96 is an independent prognostic risk factor for patients with ACS undergoing PCI and may be a novel marker for clinical practice.

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          Most cited references33

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          Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease.

          Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved.
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            Low-Dose Methotrexate for the Prevention of Atherosclerotic Events

            Inflammation is causally related to atherothrombosis. Treatment with canakinumab, a monoclonal antibody that inhibits inflammation by neutralizing interleukin-1β, resulted in a lower rate of cardiovascular events than placebo in a previous randomized trial. We sought to determine whether an alternative approach to inflammation inhibition with low-dose methotrexate might provide similar benefit.
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              T cell subsets and functions in atherosclerosis

              Atherosclerosis is a chronic inflammatory disease of the arterial wall and the primary underlying cause of cardiovascular diseases. Approaches including in vivo imaging, cell-lineage tracing and knockout studies in mice, as well as clinical interventional studies and advanced mRNA sequencing techniques have drawn attention to the role of T cells as critical drivers and modifiers of the pathogenesis of atherosclerosis. CD4 + T cells are commonly found in atherosclerotic plaques. A large body of evidence indicates that T helper 1 (T H 1) cells have pro-atherogenic roles and regulatory T (T reg ) cells anti-atherogenic roles. However, T reg cells can become pro-atherogenic. The roles in atherosclerosis of other T H cell subsets such as T H 2, T H 9, T H 17, T H 22, follicular helper T cells and CD28 – T cells, as well as other T cell subsets including CD8 + T cells and γδT cells, are less well understood. Moreover, some T cells seem to have both pro-atherogenic and anti-atherogenic functions. In this Review, we summarize the knowledge on T cell subsets, their functions in atherosclerosis and the process of T cell homing to atherosclerotic plaques. Much of our understanding of T cell roles in atherosclerosis is based on findings from experimental models. Translating these findings into human disease is challenging, but much needed. Targeting T cells and their specific cytokines are attractive pathways for developing new preventative and therapeutic approaches including potential T cell-related therapies for atherosclerosis.
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                Author and article information

                Journal
                J Inflamm Res
                J Inflamm Res
                jir
                Journal of Inflammation Research
                Dove
                1178-7031
                23 August 2023
                2023
                : 16
                : 3631-3641
                Affiliations
                [1 ]Department of Cardiology, The Affiliated Hospital of Chengde Medical University, The Chengde Institute of Cardiovascular Diseases , Chengde, Hebei, 067000, People’s Republic of China
                [2 ]Department of Clinical Laboratory, The Affiliated Hospital of Chengde Medical University , Chengde, Hebei, 067000, People’s Republic of China
                Author notes
                Correspondence: Lixian Sun, Department of Cardiology, The Affiliated Hospital of Chengde Medical University , Chengde, Hebei, 067000, People’s Republic of China, Tel +86 314 227 9016, Fax +86 314 227 4895, Email lixiansun01@126.com
                Author information
                http://orcid.org/0000-0002-6169-665X
                http://orcid.org/0000-0001-7615-4215
                http://orcid.org/0000-0001-9814-0965
                Article
                421021
                10.2147/JIR.S421021
                10460579
                37641701
                b814c20a-d21d-4841-bebd-595627ad71a1
                © 2023 Wang et al.

                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/). 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).

                History
                : 28 May 2023
                : 15 August 2023
                Page count
                Figures: 6, Tables: 4, References: 33, Pages: 11
                Funding
                Funded by: the Natural Science Foundation of Hebei Provinc;
                Funded by: Dr. Lixian Sun;
                This study was supported by the Natural Science Foundation of Hebei Province (grant number H2021406071) to Dr. Lixian Sun.
                Categories
                Original Research

                Immunology
                acute coronary syndrome,advanced lung cancer inflammation index,prognosis,percutaneous coronary intervention

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