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2016 | 63 | 3 | 555-563

Article title

High density lipoprotein subfractions and paraoxonase 1 in children

Content

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EN

Abstracts

EN
The Lipoprint system (Quantimetrix Corp., CA, USA), enables the determination of 10 high density lipoprotein (HDL) subfractions in contrast to the 5 HDL subfractions that can be determined by ultracentrifuge analysis. HDL subfractions, and their relationships to the arylesterase (PON1-A) and lactonase (PON1-L) activities of paraoxonase 1 (PON1), together with total-, very low density lipoprotein- and low density lipoprotein (LDL)-cholesterol and LDL subfractions were investigated in the serum of 27 mildly hypercholesterolemic children and 21 healthy controls. Our results suggest the antiatherogenity of large HDL (L-HDL) subfractions and the atherogenity of small HDL (S-HDL) subfractions in the study groups. However, the relationship between the intermediate HDL (I-HDL) subfractions with the LDL subfractions and other lipoproteins did not suggest that I-HDL subfractions are antiatherogenic. No significant association between PON1-A and the HDL subfractions was found. In contrast, PON1-L activity positively correlated with the antiatherogenic large HDL1 subfraction and negatively with intermediate HDL subfractions 4, 5 and 6. Our results contribute to the knowledge of the roles of total HDL and ten individual HDL subfractions in children and adolescents.

Year

Volume

63

Issue

3

Pages

555-563

Physical description

Dates

published
2016
received
2015-12-08
revised
2016-02-18
accepted
2016-02-25
(unknown)
2016-06-06

Contributors

author
  • Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Faculty of Medicine, Comenius University, Bratislava, Slovakia
  • Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Faculty of Medicine, Comenius University, Bratislava, Slovakia
  • 2nd Department of Internal Medicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia
  • Juvenalia Paediatric Centre, Dunajská Streda, Slovakia
  • Research Department, Cultech Ltd, Unit, Port Talbot SA12 7BZ, UK
  • Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Faculty of Medicine, Comenius University, Bratislava, Slovakia

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Publication order reference

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YADDA identifier

bwmeta1.element.bwnjournal-article-abpv63p555kz
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