Literature DB >> 16685079

Thematic review series: patient-oriented research. What have we learned about HDL metabolism from kinetics studies in humans?

Shirya Rashid1, Bruce W Patterson, Gary F Lewis.   

Abstract

Plasma measurements of lipids, lipoproteins, and apolipoproteins provide information on the static levels of these fractions without providing key information on the dynamic fluxes of lipoproteins in the circulation. Kinetics studies, in contrast, provide additional information on the production and clearance rates of lipoproteins and the flow of lipids and apolipoproteins through lipoprotein fractions. This information is crucial in accurately delineating the metabolism of HDL in plasma, because plasma concentrations of HDL are the net result of the de novo production and catabolism of HDL as well as the recycling of HDL particles and the contribution to HDL from components of other lipoproteins. Studies aimed at measuring the metabolism of HDL particles have shown that HDL metabolism in vivo is complex and consists of multiple components. Kinetics studies provide a window into the metabolism of HDL, allowing us to better understand the mechanisms of HDL decrease in human conditions and the functionality of HDL particles. Here, we review the progress in our understanding of HDL metabolism derived from in vivo kinetics studies, focusing primarily on studies in humans but also reviewing key studies in animal models.

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Year:  2006        PMID: 16685079     DOI: 10.1194/jlr.R600008-JLR200

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  7 in total

1.  Safety and Tolerability of ACP-501, a Recombinant Human Lecithin:Cholesterol Acyltransferase, in a Phase 1 Single-Dose Escalation Study.

Authors:  Robert D Shamburek; Rebecca Bakker-Arkema; Alexandra M Shamburek; Lita A Freeman; Marcelo J Amar; Bruce Auerbach; Brian R Krause; Reynold Homan; Steve J Adelman; Heidi L Collins; Maureen Sampson; Anna Wolska; Alan T Remaley
Journal:  Circ Res       Date:  2015-12-01       Impact factor: 17.367

2.  Sex-specific interaction between APOE genotype and carbohydrate intake affects plasma HDL-C levels: the Strong Heart Family Study.

Authors:  M J Mosher; L A Lange; B V Howard; E T Lee; L G Best; R R Fabsitz; J W Maccluer; K E North
Journal:  Genes Nutr       Date:  2008-03-29       Impact factor: 5.523

3.  LCAT cholesterol esterification is associated with the increase of ApoE/ApoA-I ratio during atherosclerosis progression in rabbit.

Authors:  Alessandro Carlucci; Luisa Cigliano; Bernardetta Maresca; Maria Stefania Spagnuolo; Giovanni Di Salvo; Raffaele Calabrò; Paolo Abrescia
Journal:  J Physiol Biochem       Date:  2012-05-05       Impact factor: 4.158

4.  Adenoviral expression of human lecithin-cholesterol acyltransferase in nonhuman primates leads to an antiatherogenic lipoprotein phenotype by increasing high-density lipoprotein and lowering low-density lipoprotein.

Authors:  Marcelo J A Amar; Robert D Shamburek; Boris Vaisman; Catherine L Knapper; Bernhard Foger; Robert F Hoyt; Silvia Santamarina-Fojo; Hollis B Brewer; Alan T Remaley
Journal:  Metabolism       Date:  2009-04       Impact factor: 8.694

Review 5.  New insights into the mechanism of low high-density lipoprotein cholesterol in obesity.

Authors:  Hao Wang; Dao-Quan Peng
Journal:  Lipids Health Dis       Date:  2011-10-12       Impact factor: 3.876

6.  Beer, wine, and spirits differentially influence body composition in older white adults-a United Kingdom Biobank study.

Authors:  Brittany A Larsen; Brandon S Klinedinst; Scott T Le; Colleen Pappas; Tovah Wolf; Nathan F Meier; Ye-Lim Lim; Auriel A Willette
Journal:  Obes Sci Pract       Date:  2022-02-16

7.  Computational lipidology: predicting lipoprotein density profiles in human blood plasma.

Authors:  Katrin Hübner; Thomas Schwager; Karl Winkler; Jens-Georg Reich; Hermann-Georg Holzhütter
Journal:  PLoS Comput Biol       Date:  2008-05-23       Impact factor: 4.475

  7 in total

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