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Efficacy of alternate-day versus everyday dosing of atorvastatin
BACKGROUND: Atorvastatin has a longer duration of action than other hydroxymethylglutaryl coenzyme A reductase inhibitors. OBJECTIVES: The objective was to evaluate the efficacy of alternate day vs. daily dosing of atorvastatin for the treatment of hyperlipidemia. MATERIALS AND METHODS: In this pros...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371460/ https://www.ncbi.nlm.nih.gov/pubmed/22701247 http://dx.doi.org/10.4103/0253-7613.96326 |
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author | Pramanik, Sushobhan Das, Asoke Kumar Chakrabarty, Milan Bandyopadhyay, Susanta Kumar Ghosh, Mainak Dalai, Chanchal Kumar |
author_facet | Pramanik, Sushobhan Das, Asoke Kumar Chakrabarty, Milan Bandyopadhyay, Susanta Kumar Ghosh, Mainak Dalai, Chanchal Kumar |
author_sort | Pramanik, Sushobhan |
collection | PubMed |
description | BACKGROUND: Atorvastatin has a longer duration of action than other hydroxymethylglutaryl coenzyme A reductase inhibitors. OBJECTIVES: The objective was to evaluate the efficacy of alternate day vs. daily dosing of atorvastatin for the treatment of hyperlipidemia. MATERIALS AND METHODS: In this prospective, open label, crossover study, 40 patients with plasma low-density cholesterol (LDL-C) of more than 130 mg/dl and total cholesterol (TC) more than 200 mg/dl were recruited. After baseline tests, they were randomly allocated to two groups. Group A received 20 mg atorvastatin on alternate days and group B received 20 mg atorvastatin daily for 12 weeks. After 4 weeks of washout period, the groups were crossed over to the other treatment regimen for another 12 weeks. Fasting plasma lipid profile and serum alanine transaminase (ALT) and aspartate transaminase (AST) were measured for both groups at 6(th), 12(th), 16(th), 22(nd), and 28(th) weeks. Results were pooled across the periods and data between the two groups were compared using unpaired t-test. RESULTS: Among the 40 enrolled subjects, 38 completed the study. Both treatment regimens significantly reduced LDL-C and TC compared to baseline. There was no statistically significant difference between the two groups in terms of reduction of plasma LDL-C and TC at 6 and 12 weeks of treatment. Both the regimens were well tolerated. CONCLUSION: Alternate-day treatment with atorvastatin is comparable in efficacy and safety to the established daily treatment regimen, thus being a cost effective alternative. |
format | Online Article Text |
id | pubmed-3371460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33714602012-06-14 Efficacy of alternate-day versus everyday dosing of atorvastatin Pramanik, Sushobhan Das, Asoke Kumar Chakrabarty, Milan Bandyopadhyay, Susanta Kumar Ghosh, Mainak Dalai, Chanchal Kumar Indian J Pharmacol Research Article BACKGROUND: Atorvastatin has a longer duration of action than other hydroxymethylglutaryl coenzyme A reductase inhibitors. OBJECTIVES: The objective was to evaluate the efficacy of alternate day vs. daily dosing of atorvastatin for the treatment of hyperlipidemia. MATERIALS AND METHODS: In this prospective, open label, crossover study, 40 patients with plasma low-density cholesterol (LDL-C) of more than 130 mg/dl and total cholesterol (TC) more than 200 mg/dl were recruited. After baseline tests, they were randomly allocated to two groups. Group A received 20 mg atorvastatin on alternate days and group B received 20 mg atorvastatin daily for 12 weeks. After 4 weeks of washout period, the groups were crossed over to the other treatment regimen for another 12 weeks. Fasting plasma lipid profile and serum alanine transaminase (ALT) and aspartate transaminase (AST) were measured for both groups at 6(th), 12(th), 16(th), 22(nd), and 28(th) weeks. Results were pooled across the periods and data between the two groups were compared using unpaired t-test. RESULTS: Among the 40 enrolled subjects, 38 completed the study. Both treatment regimens significantly reduced LDL-C and TC compared to baseline. There was no statistically significant difference between the two groups in terms of reduction of plasma LDL-C and TC at 6 and 12 weeks of treatment. Both the regimens were well tolerated. CONCLUSION: Alternate-day treatment with atorvastatin is comparable in efficacy and safety to the established daily treatment regimen, thus being a cost effective alternative. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3371460/ /pubmed/22701247 http://dx.doi.org/10.4103/0253-7613.96326 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pramanik, Sushobhan Das, Asoke Kumar Chakrabarty, Milan Bandyopadhyay, Susanta Kumar Ghosh, Mainak Dalai, Chanchal Kumar Efficacy of alternate-day versus everyday dosing of atorvastatin |
title | Efficacy of alternate-day versus everyday dosing of atorvastatin |
title_full | Efficacy of alternate-day versus everyday dosing of atorvastatin |
title_fullStr | Efficacy of alternate-day versus everyday dosing of atorvastatin |
title_full_unstemmed | Efficacy of alternate-day versus everyday dosing of atorvastatin |
title_short | Efficacy of alternate-day versus everyday dosing of atorvastatin |
title_sort | efficacy of alternate-day versus everyday dosing of atorvastatin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371460/ https://www.ncbi.nlm.nih.gov/pubmed/22701247 http://dx.doi.org/10.4103/0253-7613.96326 |
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