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. 2017 Aug 4;7:7295. doi: 10.1038/s41598-017-07821-5

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Characterization of HDL₂ and HDL₃ subfractions isolated by density gradient ultracentrifugation from seven independent pools of sera collected from healthy subjects (N), stable angina patients (SA) and acute coronary syndrome (ACS) patients. Levels of apolipoprotein AI (ApoAI) (a), ApoAII (b), ApoCIII (c), paraoxonase 1 (PON1) protein (d) and paraoxonase activity (e), and myeloperoxidase (MPO) protein (f). Data are expressed as means ± SD and analyzed with Independent Student’s T-test; *p < 0.05, **p < 0.01, ***p < 0.001 vs. N, ^#p < 0.05, ^##p < 0.01 vs. SA.