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Ezetimibe and Rosuvastatin Combination Treatment Can Reduce the Dose of Rosuvastatin Without Compromising Its Lipid-lowering Efficacy

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dc.contributor.authorRhee, Moo-Yong-
dc.contributor.authorKim, Kyung-Jin-
dc.contributor.authorKim, Sang-Hyun-
dc.contributor.authorYoon, Young Won-
dc.contributor.authorRha, Seung-Woon-
dc.contributor.authorHong, Soon Jun-
dc.contributor.authorKwak, Choong-Hwan-
dc.contributor.authorKim, Weon-
dc.contributor.authorNam, Chang-Wook-
dc.contributor.authorPark, Tae-Ho-
dc.contributor.authorHong, Taek-Jong-
dc.contributor.authorPark, Sungha-
dc.contributor.authorAhn, Youngkeun-
dc.contributor.authorLee, Namho-
dc.contributor.authorJeon, Hui-Kyung-
dc.contributor.authorJeon, Dong Woon-
dc.contributor.authorHan, Kyoo-Rok-
dc.contributor.authorMoon, Keon-Woong-
dc.contributor.authorChae, In-Ho-
dc.contributor.authorKim, Hae-Young-
dc.contributor.authorKim, Hyo-Soo-
dc.date.accessioned2021-08-31T22:58:00Z-
dc.date.available2021-08-31T22:58:00Z-
dc.date.created2021-06-18-
dc.date.issued2019-12-
dc.identifier.issn0149-2918-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/61525-
dc.description.abstractPurpose: The goal of this study was to compare the lipid-lowering efficacy of the combination of ezetimibe and low- or intermediate-intensity statin therapy versus that of high-intensity statin monotherapy. Methods: This study is a post hoc analysis of an 8 week, randomized, double-blind, Phase III trial. Patients who had hypercholesterolemia and required lipid-lowering treatment were randomly assigned to 1 of 6 treatment groups: rosuvastatin 5 mg (R5, n = 68), rosuvastatin 10 mg (R10, n = 67), rosuvastatin 20 mg (R20, n = 69), and ezetimibe 10 mg combined with rosuvastatin 5 mg (R5 + E10, n = 67), rosuvastatin 10 mg (R10 + E10, n = 68), and rosuvastatin 20 mg (R20 + E10, n = 68) daily. The effects of coadministration of ezetimibe and a low dose of rosuvastatin on lipid parameters and the target achievement rate were compared between the R5 + E10 and R10 treatment groups, the R5 + E10 and R20 treatment groups, and the R10 + E10 and R20 treatment groups. Findings: Reductions in total cholesterol, LDL-C, apolipoprotein B, the apolipoprotein B/A1 ratio, and non HDL-C were not different between the R5 + E10 and R10 treatment groups (all, P > 0.017), the R5 + E10 and R20 treatment groups (all, P > 0.017), and the R10 + E10 and R20 treatment groups (all, P > 0.017). R5 + E10 treatment showed efficacy comparable to that of R10 or R20 in affording LDL levels <50% of the baseline level (R5 + E10 vs R10, 73.13% vs 62.69% [P = 0.1952]; R5 + E10 vs R20, 73.13% vs 73.91% [P = 0.9180]), LDL-C levels <70 mg/dL (R5 + E10 vs R10, 64.18% vs 55.22% [P = 0.2906]; R5 + E10 vs R20, 64.18% vs 62.32% [P = 0.8220]), and LDL-C levels <50% of the baseline level or <70 mg/dL (R5 + E10 vs R10, 77.61% vs 70.15% [P = 0.3255]; R5 + E10 vs R20, 77.61% vs 78.26% [P = 0.9273]). The R10 + E10 treatment group was better than the R20 treatment group in achieving the target LDL-C level <70 mg/dL (83.82% vs 62.32%; P =- 0.0046), even among participants with a baseline LDL-C level >135 mg/dL (77.5% vs 48.8%, respectively; P = 0.0074). Implications: Ezetimibe combined with low- or intermediate-intensity statin therapy has lipid-lowering efficacy comparable to or better than that of high-intensity rosuvastatin monotherapy. The results of the present study indicate that the combination treatment with ezetimibe is advantageous in that it permits dose reduction of rosuvastatin without compromising the lipid-lowering efficacy of rosuvastatin. (C) 2019 Published by Elsevier Inc.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.subjectDENSITY-LIPOPROTEIN CHOLESTEROL-
dc.subjectSTATIN THERAPY-
dc.subjectLDL-C-
dc.subjectRISK-
dc.subjectMANAGEMENT-
dc.titleEzetimibe and Rosuvastatin Combination Treatment Can Reduce the Dose of Rosuvastatin Without Compromising Its Lipid-lowering Efficacy-
dc.typeArticle-
dc.contributor.affiliatedAuthorRha, Seung-Woon-
dc.contributor.affiliatedAuthorHong, Soon Jun-
dc.contributor.affiliatedAuthorKim, Hae-Young-
dc.identifier.doi10.1016/j.clinthera.2019.10.010-
dc.identifier.scopusid2-s2.0-85075495974-
dc.identifier.wosid000505107100012-
dc.identifier.bibliographicCitationCLINICAL THERAPEUTICS, v.41, no.12, pp.2571 - 2592-
dc.relation.isPartOfCLINICAL THERAPEUTICS-
dc.citation.titleCLINICAL THERAPEUTICS-
dc.citation.volume41-
dc.citation.number12-
dc.citation.startPage2571-
dc.citation.endPage2592-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusDENSITY-LIPOPROTEIN CHOLESTEROL-
dc.subject.keywordPlusSTATIN THERAPY-
dc.subject.keywordPlusLDL-C-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordAuthorCombination therapy-
dc.subject.keywordAuthorEzetimibe-
dc.subject.keywordAuthorHypercholesterolemia-
dc.subject.keywordAuthorRosuvastatin-
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