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      Relationship between HDL Cholesterol Efflux Capacity, Calcium Coronary Artery Content, and Antibodies against ApolipoproteinA-1 in Obese and Healthy Subjects

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          Abstract

          Aims: To explore the associations between cholesterol efflux capacity (CEC), coronary artery calcium (CAC) score, Framingham risk score (FRS), and antibodies against apolipoproteinA-1 (anti-apoA-1 IgG) in healthy and obese subjects (OS). Methods and Results: ABCA1-, ABCG1-, passive diffusion (PD)-CEC and anti-apoA-1 IgG were measured in sera from 34 controls and 35 OS who underwent CAC score determination by chest computed tomography. Anti-apoA-1 IgG ability to modulate CEC and macrophage cholesterol content (MCC) was tested in vitro. Controls and OS displayed similar ABCG1-, ABCA1-, PD-CEC, CAC and FRS scores. Logistic regression analyses indicated that FRS was the only significant predictor of CAC lesion. Overall, anti-apoA-1 IgG were significantly correlated with ABCA1-CEC ( r = 0.48, p < 0.0001), PD-CEC ( r = −0.33, p = 0.004), and the CAC score ( r = 0.37, p = 0.03). ABCA1-CEC was correlated with CAC score ( r = 0.47, p = 0.004) and FRS ( r = 0.18, p = 0.29), while PD-CEC was inversely associated with the same parameters (CAC: r = −0.46, p = 0.006; FRS: score r = −0.40, p = 0.01). None of these associations was replicated in healthy controls or after excluding anti-apoA-1 IgG seropositive subjects. In vitro, anti-apoA-1 IgG inhibited PD-CEC ( p < 0.0001), increased ABCA1-CEC ( p < 0.0001), and increased MCC ( p < 0.0001). Conclusions: We report a paradoxical positive association between ABCA1-CEC and the CAC score, with the latter being inversely associated with PD in OS. Corroborating our clinical observations, anti-apoA-1 IgG enhanced ABCA1 while repressing PD-CEC, leading to MCC increase in vitro. These results indicate that anti-apoA-1 IgG have the potential to interfere with CEC and macrophage lipid metabolism, and may underpin paradoxical associations between ABCA1-CEC and cardiovascular risk.

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          Most cited references38

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          A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples.

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            2010 ACCF/AHA guideline for assessment of cardiovascular risk in asymptomatic adults: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.

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              Molecular Mechanisms of Cellular Cholesterol Efflux*

              Most types of cells in the body do not express the capability of catabolizing cholesterol, so cholesterol efflux is essential for homeostasis. For instance, macrophages possess four pathways for exporting free (unesterified) cholesterol to extracellular high density lipoprotein (HDL). The passive processes include simple diffusion via the aqueous phase and facilitated diffusion mediated by scavenger receptor class B, type 1 (SR-BI). Active pathways are mediated by the ATP-binding cassette (ABC) transporters ABCA1 and ABCG1, which are membrane lipid translocases. The efflux of cellular phospholipid and free cholesterol to apolipoprotein A-I promoted by ABCA1 is essential for HDL biogenesis. Current understanding of the molecular mechanisms involved in these four efflux pathways is presented in this minireview.
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                Author and article information

                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                15 August 2019
                August 2019
                : 8
                : 8
                : 1225
                Affiliations
                [1 ]Division of Laboratory Medicine, Diagnostic Department, Geneva University Hospitals, 1211 Geneva, Switzerland
                [2 ]Division of Laboratory Medicine, Department of Medical Specialties, Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland
                [3 ]First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, 6 viale Benedetto XV, 16132 Genoa, Italy
                [4 ]Ospedale Policlinico San Martino, Genoa, 10 Largo Benzi, 16132 Genoa, Italy
                [5 ]Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 9 viale Benedetto XV, 16132 Genoa, Italy
                [6 ]Division of Cardiology, “SS. Antonio e Biagio e Cesare Arrigo” Hospital, 6 via Venezia 16, 15121 Alessandria, Italy
                [7 ]Division of Nuclear Medicine—Cardiovascular Section, Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, JHOC 3225, 601 N. Caroline Street, Baltimore, MD 21287, USA
                [8 ]Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA
                [9 ]Division of Cardiology, Cardiology Center, Geneva University Hospital, 1211 Geneva, Switzerland
                [10 ]Department of Food and Drug, University of Parma, Parco Area delle Scienze, 43124 Parma 27/A, Italy
                Author notes
                [* ]Correspondence: Sabrina.Pagano@ 123456hcuge.ch ; Tel.: +41-2237-95321
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0001-7075-1182
                https://orcid.org/0000-0003-0823-8729
                https://orcid.org/0000-0002-2141-7716
                Article
                jcm-08-01225
                10.3390/jcm8081225
                6722652
                31443207
                e96cc797-466e-44f2-8334-024048c2bac6
                © 2019 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
                : 25 June 2019
                : 12 August 2019
                Categories
                Article

                cholesterol efflux capacity,coronary artery calcium score,obesity,anti-apoa-1 igg,autoantibodies

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