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Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo
Lipoprotein (a) [Lp(a)] is a low density lipoprotein (LDL) with one apolipoprotein (a) molecule bound to the apolipoprotein B-100 of LDL. Lp(a) is an independent risk factor for cardiovascular disease (CVD). However, the relationship of Lp(a) to diabetes and metabolic syndrome, both known for increa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060502/ https://www.ncbi.nlm.nih.gov/pubmed/24937703 http://dx.doi.org/10.1038/srep05318 |
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author | Månsson, Marianne Kalies, Inge Bergström, Göran Schmidt, Caroline Legnehed, Anne Hultén, Lillemor Mattsson Amrot-Fors, Lena Gustafsson, David Knecht, Wolfgang |
author_facet | Månsson, Marianne Kalies, Inge Bergström, Göran Schmidt, Caroline Legnehed, Anne Hultén, Lillemor Mattsson Amrot-Fors, Lena Gustafsson, David Knecht, Wolfgang |
author_sort | Månsson, Marianne |
collection | PubMed |
description | Lipoprotein (a) [Lp(a)] is a low density lipoprotein (LDL) with one apolipoprotein (a) molecule bound to the apolipoprotein B-100 of LDL. Lp(a) is an independent risk factor for cardiovascular disease (CVD). However, the relationship of Lp(a) to diabetes and metabolic syndrome, both known for increased CVD risk, is controversial. In a population based study on type two diabetes mellitus (T2DM) development in women, Lp(a) plasma levels showed the well known skewed distribution without any relation to diabetes or impaired glucose tolerance. A modified clot lysis assay on a subset of 274 subjects showed significantly increased clot lysis times in T2DM subjects, despite inhibition of PAI-1 and TAFI. Lp(a) plasma levels significantly increased the maximal peak height of the clot lysis curve, indicating a change in clot structure. In this study Lp(a) is not related to the development of T2DM but may affect clot structure ex vivo without a prolongation of the clot lysis time. |
format | Online Article Text |
id | pubmed-4060502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40605022014-06-18 Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo Månsson, Marianne Kalies, Inge Bergström, Göran Schmidt, Caroline Legnehed, Anne Hultén, Lillemor Mattsson Amrot-Fors, Lena Gustafsson, David Knecht, Wolfgang Sci Rep Article Lipoprotein (a) [Lp(a)] is a low density lipoprotein (LDL) with one apolipoprotein (a) molecule bound to the apolipoprotein B-100 of LDL. Lp(a) is an independent risk factor for cardiovascular disease (CVD). However, the relationship of Lp(a) to diabetes and metabolic syndrome, both known for increased CVD risk, is controversial. In a population based study on type two diabetes mellitus (T2DM) development in women, Lp(a) plasma levels showed the well known skewed distribution without any relation to diabetes or impaired glucose tolerance. A modified clot lysis assay on a subset of 274 subjects showed significantly increased clot lysis times in T2DM subjects, despite inhibition of PAI-1 and TAFI. Lp(a) plasma levels significantly increased the maximal peak height of the clot lysis curve, indicating a change in clot structure. In this study Lp(a) is not related to the development of T2DM but may affect clot structure ex vivo without a prolongation of the clot lysis time. Nature Publishing Group 2014-06-17 /pmc/articles/PMC4060502/ /pubmed/24937703 http://dx.doi.org/10.1038/srep05318 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Månsson, Marianne Kalies, Inge Bergström, Göran Schmidt, Caroline Legnehed, Anne Hultén, Lillemor Mattsson Amrot-Fors, Lena Gustafsson, David Knecht, Wolfgang Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
title | Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
title_full | Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
title_fullStr | Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
title_full_unstemmed | Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
title_short | Lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
title_sort | lp(a) is not associated with diabetes but affects fibrinolysis and clot structure ex vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060502/ https://www.ncbi.nlm.nih.gov/pubmed/24937703 http://dx.doi.org/10.1038/srep05318 |
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