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Forecasting Cholesterol Management-End of the Statin Gold Rush?

For the last 15 years or more, lowering the low-density lipoprotein (LDL) component of total serum cholesterol has been the principal focus in cholesterol management. Ever more powerful HMG CoA reductase inhibitors (statins) captured attention in their ability to lower LDL cholesterol (LDL-C). Simva...

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Detalles Bibliográficos
Autores principales: Crownover, Brian K., Curtiss, Frederic R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Managed Care Pharmacy 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438089/
https://www.ncbi.nlm.nih.gov/pubmed/16925456
http://dx.doi.org/10.18553/jmcp.2006.12.6.479
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author Crownover, Brian K.
Curtiss, Frederic R.
author_facet Crownover, Brian K.
Curtiss, Frederic R.
author_sort Crownover, Brian K.
collection PubMed
description For the last 15 years or more, lowering the low-density lipoprotein (LDL) component of total serum cholesterol has been the principal focus in cholesterol management. Ever more powerful HMG CoA reductase inhibitors (statins) captured attention in their ability to lower LDL cholesterol (LDL-C). Simvastatin was approved by the U.S. Food and Drug Administration (FDA) 15 years ago, on December 23, 1991, with evidence of LDL-C lowering of an average 41% at the 40 mg daily dose and 47% at the maximum 80 mg daily dose.1 Lovastatin, the preceding leader in the statin market, approved by the FDA 4 years earlier, on August 13, 1987, reduced LDL-C by an average 30% at the 40 mg daily dose and by 40% when taken twice daily (80 mg daily dose)2,3 (Table 1).
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spelling pubmed-104380892023-08-21 Forecasting Cholesterol Management-End of the Statin Gold Rush? Crownover, Brian K. Curtiss, Frederic R. J Manag Care Pharm Editorials For the last 15 years or more, lowering the low-density lipoprotein (LDL) component of total serum cholesterol has been the principal focus in cholesterol management. Ever more powerful HMG CoA reductase inhibitors (statins) captured attention in their ability to lower LDL cholesterol (LDL-C). Simvastatin was approved by the U.S. Food and Drug Administration (FDA) 15 years ago, on December 23, 1991, with evidence of LDL-C lowering of an average 41% at the 40 mg daily dose and 47% at the maximum 80 mg daily dose.1 Lovastatin, the preceding leader in the statin market, approved by the FDA 4 years earlier, on August 13, 1987, reduced LDL-C by an average 30% at the 40 mg daily dose and by 40% when taken twice daily (80 mg daily dose)2,3 (Table 1). Academy of Managed Care Pharmacy 2006-07 /pmc/articles/PMC10438089/ /pubmed/16925456 http://dx.doi.org/10.18553/jmcp.2006.12.6.479 Text en Copyright © 2006, Academy of Managed Care Pharmacy. All rights reserved. https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Editorials
Crownover, Brian K.
Curtiss, Frederic R.
Forecasting Cholesterol Management-End of the Statin Gold Rush?
title Forecasting Cholesterol Management-End of the Statin Gold Rush?
title_full Forecasting Cholesterol Management-End of the Statin Gold Rush?
title_fullStr Forecasting Cholesterol Management-End of the Statin Gold Rush?
title_full_unstemmed Forecasting Cholesterol Management-End of the Statin Gold Rush?
title_short Forecasting Cholesterol Management-End of the Statin Gold Rush?
title_sort forecasting cholesterol management-end of the statin gold rush?
topic Editorials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438089/
https://www.ncbi.nlm.nih.gov/pubmed/16925456
http://dx.doi.org/10.18553/jmcp.2006.12.6.479
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