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dc.contributor.authorLappegård, Knut Tore
dc.contributor.authorKjellmo, Christian Abendstein
dc.contributor.authorHovland, Anders
dc.date.accessioned2023-01-06T13:51:11Z
dc.date.available2023-01-06T13:51:11Z
dc.date.created2021-09-24T17:31:23Z
dc.date.issued2021
dc.identifier.citationBiomedicines. 2021, 9 (7)en_US
dc.identifier.urihttps://hdl.handle.net/11250/3041638
dc.description.abstractHigh-density lipoproteins (HDL) are a heterogenous group of plasma molecules with a large variety in composition. There is a wide specter in lipid content and the number of different proteins that has been associated with HDL is approaching 100. Given this heterogeneity and the fact that the total amount of HDL is inversely related to the risk of coronary heart disease (CHD), there has been increasing interest in the function of specific HDL subgroups and in what way measuring and quantifying these subgroups could be of clinical importance in determining individual CHD risk. If certain subgroups appear to be more protective than others, it may also in the future be possible to pharmacologically increase beneficial and decrease harmful subgroups in order to reduce CHD risk. In this review we give a short historical perspective, summarize some of the recent clinical findings regarding HDL subclassifications and discuss why such classification may or may not be of clinical relevance.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleHigh-density lipoprotein subfractions: Much ado about nothing or clinically important?en_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber0en_US
dc.source.volume9en_US
dc.source.journalBiomedicinesen_US
dc.source.issue7en_US
dc.identifier.doi10.3390/biomedicines9070836
dc.identifier.cristin1938432
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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