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      The Paradox Effect of Calcification in Carotid Atherosclerosis: Microcalcification Is Correlated with Plaque Instability

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          Abstract

          Background: this study aims to investigate the possible association among the histopathologic features of carotid plaque instability, the presence of micro- or macrocalcifications, the expression of in situ inflammatory biomarkers, and the occurrence of the major risk factors in this process in a large series of carotid plaques. Methods: a total of 687 carotid plaques from symptomatic and asymptomatic patients were collected. Histological evaluation was performed to classify the calcium deposits in micro or macrocalcifications according to their morphological features (location and size). Immunohistochemistry was performed to study the expression of the main inflammatory biomarkers. Results: results here reported demonstrated that calcifications are very frequent in carotid plaques, with a significant difference between the presence of micro- and macrocalcifications. Specifically, microcalcifications were significantly associated to high inflamed unstable plaques. Paradoxically, macrocalcifications seem to stabilize the plaque and are associated to a M2 macrophage polarization instead. Discussion: the characterization of mechanisms involved in the formation of carotid calcifications can lay the foundation for developing new strategies for the management of patients affected by carotid atherosclerosis. Data of this study could provide key elements for an exhaustive evaluation of carotid plaque calcifications allowing to establish the risk of associated clinical events.

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          Most cited references42

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          Macrophage plasticity, polarization, and function in health and disease.

          Macrophages are heterogeneous and their phenotype and functions are regulated by the surrounding micro-environment. Macrophages commonly exist in two distinct subsets: 1) Classically activated or M1 macrophages, which are pro-inflammatory and polarized by lipopolysaccharide (LPS) either alone or in association with Th1 cytokines such as IFN-γ, GM-CSF, and produce pro-inflammatory cytokines such as interleukin-1β (IL-1β), IL-6, IL-12, IL-23, and TNF-α; and 2) Alternatively activated or M2 macrophages, which are anti-inflammatory and immunoregulatory and polarized by Th2 cytokines such as IL-4 and IL-13 and produce anti-inflammatory cytokines such as IL-10 and TGF-β. M1 and M2 macrophages have different functions and transcriptional profiles. They have unique abilities by destroying pathogens or repair the inflammation-associated injury. It is known that M1/M2 macrophage balance polarization governs the fate of an organ in inflammation or injury. When the infection or inflammation is severe enough to affect an organ, macrophages first exhibit the M1 phenotype to release TNF-α, IL-1β, IL-12, and IL-23 against the stimulus. But, if M1 phase continues, it can cause tissue damage. Therefore, M2 macrophages secrete high amounts of IL-10 and TGF-β to suppress the inflammation, contribute to tissue repair, remodeling, vasculogenesis, and retain homeostasis. In this review, we first discuss the basic biology of macrophages including origin, differentiation and activation, tissue distribution, plasticity and polarization, migration, antigen presentation capacity, cytokine and chemokine production, metabolism, and involvement of microRNAs in macrophage polarization and function. Secondly, we discuss the protective and pathogenic role of the macrophage subsets in normal and pathological pregnancy, anti-microbial defense, anti-tumor immunity, metabolic disease and obesity, asthma and allergy, atherosclerosis, fibrosis, wound healing, and autoimmunity.
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            Macrophage Polarization.

            Macrophage polarization refers to how macrophages have been activated at a given point in space and time. Polarization is not fixed, as macrophages are sufficiently plastic to integrate multiple signals, such as those from microbes, damaged tissues, and the normal tissue environment. Three broad pathways control polarization: epigenetic and cell survival pathways that prolong or shorten macrophage development and viability, the tissue microenvironment, and extrinsic factors, such as microbial products and cytokines released in inflammation. A plethora of advances have provided a framework for rationally purifying, describing, and manipulating macrophage polarization. Here, I assess the current state of knowledge about macrophage polarization and enumerate the major questions about how activated macrophages regulate the physiology of normal and damaged tissues.
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              Coronary Calcium Score and Cardiovascular Risk

              Coronary artery calcium (CAC) is a highly specific feature of coronary atherosclerosis. Based on single-center and multicenter clinical and population-based studies with short-term and long-term outcomes data (up to 15 years follow-up), CAC scoring has emerged as a widely available, consistent, and reproducible means of assessing risk of major cardiovascular outcomes, especially useful in asymptomatic people for planning primary prevention interventions such as statins and aspirin. CAC testing in asymptomatic populations is cost-effective across a broad range of baseline risk. This review summarizes evidence concerning CAC, including its pathobiology, modalities for detection, predictive role, use in prediction scoring algorithms, CAC progression, evidence that CAC changes the clinical approach to the patient and patient behavior, novel applications of CAC, future directions in scoring CAC scans, and new CAC guidelines.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                01 January 2021
                January 2021
                : 22
                : 1
                : 395
                Affiliations
                [1 ]Department of Experimental Medicine, University “Tor Vergata”, Via Montpellier 1, 00133 Rome, Italy; manuela.montanaro@ 123456uniroma2.it (M.M.); manuel.scimeca@ 123456uniroma2.it (M.S.); anemona@ 123456uniroma2.it (L.A.); francesca.servadei@ 123456ptvonline.it (F.S.); erica.giacobbi@ 123456ptvonline.it (E.G.); rita.bonfiglio@ 123456uniroma2.it (R.B.); elena.bonanno@ 123456uniroma2.it (E.B.); santeusa@ 123456uniroma2.it (G.S.)
                [2 ]Saint Camillus International University of Health Sciences, Via di Sant’Alessandro 8, 00131 Rome, Italy
                [3 ]Fondazione Umberto Veronesi (FUV), Piazza Velasca 5, 20122 Milano, Italy
                [4 ]Nuclear Medicine Unit, Department of Oncohaematology, Policlinico “Tor Vergata”, viale oxford 81, 00133 Rome, Italy; n.urbano@ 123456virgilio.it
                [5 ]Vascular Surgery, Department of Biomedicine and Prevention, Policlinico “Tor Vergata”, viale oxford 81, 00133 Rome, Italy; ippoliti@ 123456med.uniroma2.it
                [6 ]Department of Biomedicine and Prevention, University of Rome “Tor Vergata”, Via Montpellier 1, 00133 Rome, Italy; orazio.schillaci@ 123456uniroma2.it
                [7 ]IRCCS Neuromed, 86077 Pozzilli, Italy
                Author notes
                [* ]Correspondence: alessandro.mauriello@ 123456uniroma2.it ; Tel.: +39-0620903908
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-0585-1309
                https://orcid.org/0000-0002-3711-2714
                https://orcid.org/0000-0003-2619-9153
                https://orcid.org/0000-0002-2582-3527
                https://orcid.org/0000-0002-7351-5676
                Article
                ijms-22-00395
                10.3390/ijms22010395
                7796057
                33401449
                8794acf5-d054-4589-850b-8c0ed1790d19
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 30 November 2020
                : 28 December 2020
                Categories
                Article

                Molecular biology
                atherosclerosis,plaque instability,carotid plaque,microcalcification,macrocalcification,macrophage polarization,inflammatory biomarkers

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