Cargando…

Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy

BACKGROUND: Many high-risk coronary heart disease (CHD) patients on statin monotherapy do not achieve guideline-recommended low-density lipoprotein cholesterol (LDL-C) goals, and combination lipid-lowering therapy may be considered for these individuals. The effect of adding ezetimibe to simvastatin...

Descripción completa

Detalles Bibliográficos
Autores principales: Foody, JoAnne M, Toth, Peter P, Tomassini, Joanne E, Sajjan, Shiva, Ramey, Dena R, Neff, David, Tershakovec, Andrew M, Hu, Henry, Tunceli, Kaan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833706/
https://www.ncbi.nlm.nih.gov/pubmed/24265554
http://dx.doi.org/10.2147/VHRM.S49840
_version_ 1782291882414440448
author Foody, JoAnne M
Toth, Peter P
Tomassini, Joanne E
Sajjan, Shiva
Ramey, Dena R
Neff, David
Tershakovec, Andrew M
Hu, Henry
Tunceli, Kaan
author_facet Foody, JoAnne M
Toth, Peter P
Tomassini, Joanne E
Sajjan, Shiva
Ramey, Dena R
Neff, David
Tershakovec, Andrew M
Hu, Henry
Tunceli, Kaan
author_sort Foody, JoAnne M
collection PubMed
description BACKGROUND: Many high-risk coronary heart disease (CHD) patients on statin monotherapy do not achieve guideline-recommended low-density lipoprotein cholesterol (LDL-C) goals, and combination lipid-lowering therapy may be considered for these individuals. The effect of adding ezetimibe to simvastatin, atorvastatin, or rosuvastatin therapy versus titrating these statins on LDL-C changes and goal attainment in CHD or CHD risk-equivalent patients was assessed in a large, managed-care database in the US. METHODS: Eligible patients (n = 17,830), initially on statin monotherapy who were ≥18 years with baseline and follow-up LDL-C values, no concomitant use of other lipid-lowering therapy, and on lipid-lowering therapy for ≥42 days, were identified between November 1, 2002 and September 30, 2009. The percent change from baseline in LDL-C levels and the odds ratios for attainment of LDL-C <1.8 and <2.6 mmol/L (70 and 100 mg/dL) were estimated using an analysis of covariance and logistic regression, respectively, adjusted for various baseline factors. RESULTS: LDL-C reductions from baseline and goal attainment improved substantially in patients treated with ezetimibe added onto simvastatin, atorvastatin, or rosuvastatin therapy (n = 2,312) versus those (n = 13,053) who titrated these statins. In multivariable models, percent change from baseline in LDL-C was −13.1% to −14.8% greater for those who added ezetimibe onto simvastatin, atorvastatin, or rosuvastatin versus those who titrated. The odds of attaining LDL-C <1.8 and <2.6 mmol/L (70 and 100 mg/dL) increased by 2.6–3.2-fold and 2.5–3.1-fold, respectively, in patients who added ezetimibe onto simvastatin, atorvastatin, or rosuvastatin versus titrating statins. CONCLUSION: CHD/CHD risk-equivalent patients in a large US managed-care database, who added ezetimibe onto simvastatin, atorvastatin, or rosuvastatin, had greater LDL-C reductions and goal attainment than those who uptitrated these statin therapies. Our study suggests that high-risk CHD patients in need of more intensive LDL-C lowering therapy may benefit by adding ezetimibe onto statin therapy.
format Online
Article
Text
id pubmed-3833706
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-38337062013-11-21 Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy Foody, JoAnne M Toth, Peter P Tomassini, Joanne E Sajjan, Shiva Ramey, Dena R Neff, David Tershakovec, Andrew M Hu, Henry Tunceli, Kaan Vasc Health Risk Manag Original Research BACKGROUND: Many high-risk coronary heart disease (CHD) patients on statin monotherapy do not achieve guideline-recommended low-density lipoprotein cholesterol (LDL-C) goals, and combination lipid-lowering therapy may be considered for these individuals. The effect of adding ezetimibe to simvastatin, atorvastatin, or rosuvastatin therapy versus titrating these statins on LDL-C changes and goal attainment in CHD or CHD risk-equivalent patients was assessed in a large, managed-care database in the US. METHODS: Eligible patients (n = 17,830), initially on statin monotherapy who were ≥18 years with baseline and follow-up LDL-C values, no concomitant use of other lipid-lowering therapy, and on lipid-lowering therapy for ≥42 days, were identified between November 1, 2002 and September 30, 2009. The percent change from baseline in LDL-C levels and the odds ratios for attainment of LDL-C <1.8 and <2.6 mmol/L (70 and 100 mg/dL) were estimated using an analysis of covariance and logistic regression, respectively, adjusted for various baseline factors. RESULTS: LDL-C reductions from baseline and goal attainment improved substantially in patients treated with ezetimibe added onto simvastatin, atorvastatin, or rosuvastatin therapy (n = 2,312) versus those (n = 13,053) who titrated these statins. In multivariable models, percent change from baseline in LDL-C was −13.1% to −14.8% greater for those who added ezetimibe onto simvastatin, atorvastatin, or rosuvastatin versus those who titrated. The odds of attaining LDL-C <1.8 and <2.6 mmol/L (70 and 100 mg/dL) increased by 2.6–3.2-fold and 2.5–3.1-fold, respectively, in patients who added ezetimibe onto simvastatin, atorvastatin, or rosuvastatin versus titrating statins. CONCLUSION: CHD/CHD risk-equivalent patients in a large US managed-care database, who added ezetimibe onto simvastatin, atorvastatin, or rosuvastatin, had greater LDL-C reductions and goal attainment than those who uptitrated these statin therapies. Our study suggests that high-risk CHD patients in need of more intensive LDL-C lowering therapy may benefit by adding ezetimibe onto statin therapy. Dove Medical Press 2013 2013-11-15 /pmc/articles/PMC3833706/ /pubmed/24265554 http://dx.doi.org/10.2147/VHRM.S49840 Text en © 2013 Foody et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed.
spellingShingle Original Research
Foody, JoAnne M
Toth, Peter P
Tomassini, Joanne E
Sajjan, Shiva
Ramey, Dena R
Neff, David
Tershakovec, Andrew M
Hu, Henry
Tunceli, Kaan
Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
title Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
title_full Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
title_fullStr Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
title_full_unstemmed Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
title_short Changes in LDL-C levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
title_sort changes in ldl-c levels and goal attainment associated with addition of ezetimibe to simvastatin, atorvastatin, or rosuvastatin compared with titrating statin monotherapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833706/
https://www.ncbi.nlm.nih.gov/pubmed/24265554
http://dx.doi.org/10.2147/VHRM.S49840
work_keys_str_mv AT foodyjoannem changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT tothpeterp changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT tomassinijoannee changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT sajjanshiva changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT rameydenar changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT neffdavid changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT tershakovecandrewm changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT huhenry changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy
AT tuncelikaan changesinldlclevelsandgoalattainmentassociatedwithadditionofezetimibetosimvastatinatorvastatinorrosuvastatincomparedwithtitratingstatinmonotherapy