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Harangi et al. Vessel Plus 2017;1:166-73                                          Vessel Plus
           DOI: 10.20517/2574-1209.2017.27
                                                                                                  www.vpjournal.net
            Topic: Atherosclerosis and Related Diseases                                         Open Access

           HDL subfraction distribution and HDL

           function in untreated dyslipidemic

           patients



           Mariann Harangi, Anita Szentpéteri, Bíborka Nádró, Hajnalka Lőrincz, Ildikó Seres, Dénes Páll, György Paragh

           Department of Internal Medicine, University of Debrecen Faculty of Medicine, H-4032 Debrecen, Hungary.
           Correspondence to: Dr. Mariann Harangi, Department of Internal Medicine, University of Debrecen Faculty of Medicine, Nagyerdei krt. 98, H-4032
           Debrecen, Hungary. E-mail: mharangi@hotmail.com

           How to cite this article: Harangi M, Szentpéteri A, Nádró B, Lőrincz H, Seres I, Páll D, Paragh G. HDL subfraction distribution and HDL function
           in untreated dyslipidemic patients. Vessel Plus 2017;1:166-73.

                                         ABSTRACT
            Article history:              Aim: The protective role of high-density lipoprotein (HDL) against atherosclerosis is well
            Received: 31 Jul 2017         known. However, both structural and functional changes of the HDL particles may affect its
            Accepted: 18 Sep 2017         protective efficacy. Increased levels of HDL-associated myeloperoxidase (MPO) and decreased
            Published: 28 Dec 2017        HDL-linked paraoxonase-1 (PON1) activity have been reported in dyslipidemic patients. Some
                                          changes in HDL subfraction distributions were also studied previously, but data on structural
            Key words:                    and functional changes in dyslipidemia are not complete. Therefore, the authors aimed to
            High-density lipoprotein,     evaluate these qualitative and quantitative markers of HDL in dyslipidemic patients and
            subfraction,                  healthy control subjects. Methods: Anthropometric parameters, serum levels of lipoproteins
            paraoxonase,
            myeloperoxidase,              and MPO, as well as PON1 activities were investigated in 81 untreated dyslipidemic patients
            dyslipidemia                  and in 32 healthy gender-matched controls. Additionally, HDL subfractions were detected
                                          by  an  electrophoretic  method  on  polyacrylamide  gel  (Lipoprint).  Results:  Significantly
                                          higher glucose, hemoglobin A1c, total cholesterol, low-density lipoprotein-cholesterol,
                                          triglyceride, lipoprotein(a), apolipoprotein B, C-reactive protein, and MPO levels were found
                                          in patients compared to the healthy subjects. There were no significant differences in PON1
                                          paraoxonase and arylesterase activities between the two study groups, but MPO/PON1 ratio
                                          was significantly higher in patients. There was a shift towards the smaller HDL subfractions,
                                          but only the intermediate HDL ratio was significantly lower in patients compared to controls.
                                          Conclusion: The results highlight the importance of HDL-associated pro- and antioxidant
                                          enzymes suggesting the possible clinical benefit of MPO/PON1 calculation and confirm that
                                          quantification of HDL-C level alone provides limited data regarding HDL’s cardioprotective
                                          effect. Calculation of MPO/PON1 ratio may be a useful cardiovascular marker in dyslipidemia.

           INTRODUCTION                                       heterogeneous in their structural, chemical and
                                                              biological properties. Using different analytical
           High-density lipoprotein (HDL) is a fraction of    methods HDL can be separated to subclasses
           small, dense, protein-rich lipoprotein that is highly   differing in size, density, shape and lipid and protein

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