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

Monitoring cholesterol levels is strongly recommended to identify patients at risk for myocardial infarction. However, clinical markers beyond "bad" and "good" cholesterol are needed to precisely predict individual lipid disorders. Our work contributes to this aim by bringing tog...

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Autores principales: Katrin Hübner, Thomas Schwager, Karl Winkler, Jens-Georg Reich, Hermann-Georg Holzhütter
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Publicado: Public Library of Science (PLoS) 2008
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Acceso en línea:https://doaj.org/article/c7916a01ea8c41c59ad14ef7ee327615
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spelling oai:doaj.org-article:c7916a01ea8c41c59ad14ef7ee3276152021-11-25T05:41:17ZComputational lipidology: predicting lipoprotein density profiles in human blood plasma.1553-734X1553-735810.1371/journal.pcbi.1000079https://doaj.org/article/c7916a01ea8c41c59ad14ef7ee3276152008-05-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18497853/?tool=EBIhttps://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358Monitoring cholesterol levels is strongly recommended to identify patients at risk for myocardial infarction. However, clinical markers beyond "bad" and "good" cholesterol are needed to precisely predict individual lipid disorders. Our work contributes to this aim by bringing together experiment and theory. We developed a novel computer-based model of the human plasma lipoprotein metabolism in order to simulate the blood lipid levels in high resolution. Instead of focusing on a few conventionally used predefined lipoprotein density classes (LDL, HDL), we consider the entire protein and lipid composition spectrum of individual lipoprotein complexes. Subsequently, their distribution over density (which equals the lipoprotein profile) is calculated. As our main results, we (i) successfully reproduced clinically measured lipoprotein profiles of healthy subjects; (ii) assigned lipoproteins to narrow density classes, named high-resolution density sub-fractions (hrDS), revealing heterogeneous lipoprotein distributions within the major lipoprotein classes; and (iii) present model-based predictions of changes in the lipoprotein distribution elicited by disorders in underlying molecular processes. In its present state, the model offers a platform for many future applications aimed at understanding the reasons for inter-individual variability, identifying new sub-fractions of potential clinical relevance and a patient-oriented diagnosis of the potential molecular causes for individual dyslipidemia.Katrin HübnerThomas SchwagerKarl WinklerJens-Georg ReichHermann-Georg HolzhütterPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 4, Iss 5, p e1000079 (2008)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Katrin Hübner
Thomas Schwager
Karl Winkler
Jens-Georg Reich
Hermann-Georg Holzhütter
Computational lipidology: predicting lipoprotein density profiles in human blood plasma.
description Monitoring cholesterol levels is strongly recommended to identify patients at risk for myocardial infarction. However, clinical markers beyond "bad" and "good" cholesterol are needed to precisely predict individual lipid disorders. Our work contributes to this aim by bringing together experiment and theory. We developed a novel computer-based model of the human plasma lipoprotein metabolism in order to simulate the blood lipid levels in high resolution. Instead of focusing on a few conventionally used predefined lipoprotein density classes (LDL, HDL), we consider the entire protein and lipid composition spectrum of individual lipoprotein complexes. Subsequently, their distribution over density (which equals the lipoprotein profile) is calculated. As our main results, we (i) successfully reproduced clinically measured lipoprotein profiles of healthy subjects; (ii) assigned lipoproteins to narrow density classes, named high-resolution density sub-fractions (hrDS), revealing heterogeneous lipoprotein distributions within the major lipoprotein classes; and (iii) present model-based predictions of changes in the lipoprotein distribution elicited by disorders in underlying molecular processes. In its present state, the model offers a platform for many future applications aimed at understanding the reasons for inter-individual variability, identifying new sub-fractions of potential clinical relevance and a patient-oriented diagnosis of the potential molecular causes for individual dyslipidemia.
format article
author Katrin Hübner
Thomas Schwager
Karl Winkler
Jens-Georg Reich
Hermann-Georg Holzhütter
author_facet Katrin Hübner
Thomas Schwager
Karl Winkler
Jens-Georg Reich
Hermann-Georg Holzhütter
author_sort Katrin Hübner
title Computational lipidology: predicting lipoprotein density profiles in human blood plasma.
title_short Computational lipidology: predicting lipoprotein density profiles in human blood plasma.
title_full Computational lipidology: predicting lipoprotein density profiles in human blood plasma.
title_fullStr Computational lipidology: predicting lipoprotein density profiles in human blood plasma.
title_full_unstemmed Computational lipidology: predicting lipoprotein density profiles in human blood plasma.
title_sort computational lipidology: predicting lipoprotein density profiles in human blood plasma.
publisher Public Library of Science (PLoS)
publishDate 2008
url https://doaj.org/article/c7916a01ea8c41c59ad14ef7ee327615
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AT karlwinkler computationallipidologypredictinglipoproteindensityprofilesinhumanbloodplasma
AT jensgeorgreich computationallipidologypredictinglipoproteindensityprofilesinhumanbloodplasma
AT hermanngeorgholzhutter computationallipidologypredictinglipoproteindensityprofilesinhumanbloodplasma
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