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Lipid apheresis: oxidative stress, rheology, and vasodilatation
In the treatment of homozygous and therapy-resistant hypercholesterolemia, lipid apheresis enables not only low density lipoprotein (LDL) cholesterol to be lowered by approximately 60%, but also oxidative stress factors to be influenced and adhesion molecules reduced. This was investigated in a grou...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374116/ https://www.ncbi.nlm.nih.gov/pubmed/22528131 http://dx.doi.org/10.1007/s11789-012-0043-9 |
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author | Mellwig, K.-P. Pulawski, E. Horstkotte, D. van Buuren, F. |
author_facet | Mellwig, K.-P. Pulawski, E. Horstkotte, D. van Buuren, F. |
author_sort | Mellwig, K.-P. |
collection | PubMed |
description | In the treatment of homozygous and therapy-resistant hypercholesterolemia, lipid apheresis enables not only low density lipoprotein (LDL) cholesterol to be lowered by approximately 60%, but also oxidative stress factors to be influenced and adhesion molecules reduced. This was investigated in a group of 12 patients using the heparin-induced extracorporeal LDL precipitation (H.E.L.P.) procedure. A significant lowering of LDL cholesterol and fibrinogen leads to an improvement in rheology and endothelial function, detectable and measurable within approximately 20 h by assessing minimum coronary resistance using positron emission tomography (PET) performed in 35 patients. This effect is detectable even after the first lipid apheresis session (H.E.L.P. procedure), documented in 12 patients. Lipid apheresis appears to be the most effective procedure in the treatment of elevated lipoprotein(a) [Lp(a)]. A chosen group of nine patients with selective elevated Lp(a) illustrated both the influence on endothelial dysfunction, in the shape of sharply increased minimum coronary resistance, and the reduction through lipid apheresis, indicating that Lp(a) seems to exert a similar effect on the vascular wall and vascular function as LDL cholesterol. |
format | Online Article Text |
id | pubmed-3374116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-33741162012-06-14 Lipid apheresis: oxidative stress, rheology, and vasodilatation Mellwig, K.-P. Pulawski, E. Horstkotte, D. van Buuren, F. Clin Res Cardiol Suppl Article In the treatment of homozygous and therapy-resistant hypercholesterolemia, lipid apheresis enables not only low density lipoprotein (LDL) cholesterol to be lowered by approximately 60%, but also oxidative stress factors to be influenced and adhesion molecules reduced. This was investigated in a group of 12 patients using the heparin-induced extracorporeal LDL precipitation (H.E.L.P.) procedure. A significant lowering of LDL cholesterol and fibrinogen leads to an improvement in rheology and endothelial function, detectable and measurable within approximately 20 h by assessing minimum coronary resistance using positron emission tomography (PET) performed in 35 patients. This effect is detectable even after the first lipid apheresis session (H.E.L.P. procedure), documented in 12 patients. Lipid apheresis appears to be the most effective procedure in the treatment of elevated lipoprotein(a) [Lp(a)]. A chosen group of nine patients with selective elevated Lp(a) illustrated both the influence on endothelial dysfunction, in the shape of sharply increased minimum coronary resistance, and the reduction through lipid apheresis, indicating that Lp(a) seems to exert a similar effect on the vascular wall and vascular function as LDL cholesterol. Springer-Verlag 2012-03-10 2012-06 /pmc/articles/PMC3374116/ /pubmed/22528131 http://dx.doi.org/10.1007/s11789-012-0043-9 Text en © The Author(s) 2012 |
spellingShingle | Article Mellwig, K.-P. Pulawski, E. Horstkotte, D. van Buuren, F. Lipid apheresis: oxidative stress, rheology, and vasodilatation |
title | Lipid apheresis: oxidative stress, rheology, and vasodilatation |
title_full | Lipid apheresis: oxidative stress, rheology, and vasodilatation |
title_fullStr | Lipid apheresis: oxidative stress, rheology, and vasodilatation |
title_full_unstemmed | Lipid apheresis: oxidative stress, rheology, and vasodilatation |
title_short | Lipid apheresis: oxidative stress, rheology, and vasodilatation |
title_sort | lipid apheresis: oxidative stress, rheology, and vasodilatation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374116/ https://www.ncbi.nlm.nih.gov/pubmed/22528131 http://dx.doi.org/10.1007/s11789-012-0043-9 |
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