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Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients
Carnitine has high dialyzability and is often deficient in dialysis patients. This deficiency is treated by either intravenous (IV) or oral supplementation of carnitine. In this study, the mode of carnitine administration was changed from oral to IV in 17 hemodialysis (HD) patients, and the treatmen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014372/ https://www.ncbi.nlm.nih.gov/pubmed/29616582 http://dx.doi.org/10.1080/0886022X.2018.1455587 |
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author | Suzuki, Anna Sakai, Yukinao Hashimoto, Kazumasa Osawa, Hirokazu Tsuruoka, Shuichi |
author_facet | Suzuki, Anna Sakai, Yukinao Hashimoto, Kazumasa Osawa, Hirokazu Tsuruoka, Shuichi |
author_sort | Suzuki, Anna |
collection | PubMed |
description | Carnitine has high dialyzability and is often deficient in dialysis patients. This deficiency is treated by either intravenous (IV) or oral supplementation of carnitine. In this study, the mode of carnitine administration was changed from oral to IV in 17 hemodialysis (HD) patients, and the treatment was discontinued after 1 year. We found that the levels of total carnitine (TC), free-carnitine (FC), and acyl-carnitine (AC) significantly increased after 3 months of switching to IV administration (p < .05). After discontinuation of carnitine administration, the TC, FC, and AC levels decreased before dialysis. The average FC value was maintained at the normal levels until 9 months, but fell below the normal values when measured at the 12th month of discontinuation. In conclusion, carnitine was maintained at significantly high levels despite the smaller dose by IV infusion as compared with that by oral administration. We therefore suggest that our results be considered while determining both the carnitine administration route and the administration period in dialysis patients under clinical settings. |
format | Online Article Text |
id | pubmed-6014372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60143722018-06-28 Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients Suzuki, Anna Sakai, Yukinao Hashimoto, Kazumasa Osawa, Hirokazu Tsuruoka, Shuichi Ren Fail Clinical Study Carnitine has high dialyzability and is often deficient in dialysis patients. This deficiency is treated by either intravenous (IV) or oral supplementation of carnitine. In this study, the mode of carnitine administration was changed from oral to IV in 17 hemodialysis (HD) patients, and the treatment was discontinued after 1 year. We found that the levels of total carnitine (TC), free-carnitine (FC), and acyl-carnitine (AC) significantly increased after 3 months of switching to IV administration (p < .05). After discontinuation of carnitine administration, the TC, FC, and AC levels decreased before dialysis. The average FC value was maintained at the normal levels until 9 months, but fell below the normal values when measured at the 12th month of discontinuation. In conclusion, carnitine was maintained at significantly high levels despite the smaller dose by IV infusion as compared with that by oral administration. We therefore suggest that our results be considered while determining both the carnitine administration route and the administration period in dialysis patients under clinical settings. Taylor & Francis 2018-04-04 /pmc/articles/PMC6014372/ /pubmed/29616582 http://dx.doi.org/10.1080/0886022X.2018.1455587 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Suzuki, Anna Sakai, Yukinao Hashimoto, Kazumasa Osawa, Hirokazu Tsuruoka, Shuichi Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
title | Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
title_full | Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
title_fullStr | Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
title_full_unstemmed | Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
title_short | Kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
title_sort | kinetics of carnitine concentration after switching from oral administration to intravenous injection in hemodialysis patients |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014372/ https://www.ncbi.nlm.nih.gov/pubmed/29616582 http://dx.doi.org/10.1080/0886022X.2018.1455587 |
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