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The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker
The use of vitamin E-bonded cellulose membrane dialyzers has been reported to cause a decrease in oxidative lipid marker levels (Nakai et al., Ther Apher Dial 14:505–540, 1; Nakai et al., J Jpn Soc Dial Ther 45:1–47, 2; Mashiba et al., Arterioscler Thromb Vasc Biol 21:1801–1808, 3). However, few stu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Japan
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684714/ https://www.ncbi.nlm.nih.gov/pubmed/23397123 http://dx.doi.org/10.1007/s10047-013-0689-1 |
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author | Kitamura, Yuki Kamimura, Kumi Yoshioka, Noriko Hosotani, Yoko Tsuchida, Kenji Koremoto, Masahide Minakuchi, Jun |
author_facet | Kitamura, Yuki Kamimura, Kumi Yoshioka, Noriko Hosotani, Yoko Tsuchida, Kenji Koremoto, Masahide Minakuchi, Jun |
author_sort | Kitamura, Yuki |
collection | PubMed |
description | The use of vitamin E-bonded cellulose membrane dialyzers has been reported to cause a decrease in oxidative lipid marker levels (Nakai et al., Ther Apher Dial 14:505–540, 1; Nakai et al., J Jpn Soc Dial Ther 45:1–47, 2; Mashiba et al., Arterioscler Thromb Vasc Biol 21:1801–1808, 3). However, few studies have identified this effect with vitamin E-bonded polysulfone membranes, and no studies report the same effect on alpha (1) antitrypsin–LDL complex, a new oxidative lipid marker. This prompted us to examine the influence of use of VPS-HA vitamin E-bonded polysulfone high-flux membrane dialyzers on this new oxidative lipid marker. The subjects were 17 patients who had been dialyzed with VPS-HA for 12 months. The subjects’ baseline characteristics were as follows. Their average age was 65.6 ± 13.1 years, comprising 8 males and 9 females; hemodialysis vintage was 83.8 ± 85.4 months. Eight had chronic glomerular nephropathy and five had diabetic nephropathy. The primary outcome was defined as alpha (1) antitrypsin–LDL complex level after 12 months, as a post-study using VPS-HA. Secondary outcomes included triglycerides, total cholesterol, HDL cholesterol and LDL cholesterol levels. The data were analyzed pre-study and after 3, 6, 9 and 12 months for alpha (1) antitrypsin–LDL complex, and pre-study and post-study for the other indicators. Twelve months after switching to VPS-HA, alpha (1) antitrypsin–LDL complex, total cholesterol and LDL cholesterol had significantly decreased. Triglycerides and HDL cholesterol had not significantly changed. Hemodialysis therapy with VPS-HA was shown to decrease alpha (1) antitrypsin–LDL complex, an index of oxidative stress, and also to decrease some lipid markers. |
format | Online Article Text |
id | pubmed-3684714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-36847142013-06-20 The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker Kitamura, Yuki Kamimura, Kumi Yoshioka, Noriko Hosotani, Yoko Tsuchida, Kenji Koremoto, Masahide Minakuchi, Jun J Artif Organs Original Article The use of vitamin E-bonded cellulose membrane dialyzers has been reported to cause a decrease in oxidative lipid marker levels (Nakai et al., Ther Apher Dial 14:505–540, 1; Nakai et al., J Jpn Soc Dial Ther 45:1–47, 2; Mashiba et al., Arterioscler Thromb Vasc Biol 21:1801–1808, 3). However, few studies have identified this effect with vitamin E-bonded polysulfone membranes, and no studies report the same effect on alpha (1) antitrypsin–LDL complex, a new oxidative lipid marker. This prompted us to examine the influence of use of VPS-HA vitamin E-bonded polysulfone high-flux membrane dialyzers on this new oxidative lipid marker. The subjects were 17 patients who had been dialyzed with VPS-HA for 12 months. The subjects’ baseline characteristics were as follows. Their average age was 65.6 ± 13.1 years, comprising 8 males and 9 females; hemodialysis vintage was 83.8 ± 85.4 months. Eight had chronic glomerular nephropathy and five had diabetic nephropathy. The primary outcome was defined as alpha (1) antitrypsin–LDL complex level after 12 months, as a post-study using VPS-HA. Secondary outcomes included triglycerides, total cholesterol, HDL cholesterol and LDL cholesterol levels. The data were analyzed pre-study and after 3, 6, 9 and 12 months for alpha (1) antitrypsin–LDL complex, and pre-study and post-study for the other indicators. Twelve months after switching to VPS-HA, alpha (1) antitrypsin–LDL complex, total cholesterol and LDL cholesterol had significantly decreased. Triglycerides and HDL cholesterol had not significantly changed. Hemodialysis therapy with VPS-HA was shown to decrease alpha (1) antitrypsin–LDL complex, an index of oxidative stress, and also to decrease some lipid markers. Springer Japan 2013-02-10 2013-06 /pmc/articles/PMC3684714/ /pubmed/23397123 http://dx.doi.org/10.1007/s10047-013-0689-1 Text en © The Japanese Society for Artificial Organs 2013 |
spellingShingle | Original Article Kitamura, Yuki Kamimura, Kumi Yoshioka, Noriko Hosotani, Yoko Tsuchida, Kenji Koremoto, Masahide Minakuchi, Jun The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
title | The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
title_full | The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
title_fullStr | The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
title_full_unstemmed | The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
title_short | The effect of vitamin E-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
title_sort | effect of vitamin e-bonded polysulfone membrane dialyzer on a new oxidative lipid marker |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684714/ https://www.ncbi.nlm.nih.gov/pubmed/23397123 http://dx.doi.org/10.1007/s10047-013-0689-1 |
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