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Combination Therapy of Rosuvastatin and Ezetimibe in Patients with High Cardiovascular Risk.
Yang, Young-June; Lee, Sang-Hak; Kim, Byung Soo; Cho, Yun-Kyeong; Cho, Hyun-Jai; Cho, Kyoung Im; Kim, Seok-Yeon; Ryu, Jae Kean; Cho, Jin-Man; Park, Joong-Il; Park, Jong-Seon; Park, Chang Gyu; Chun, Woo Jung; Kim, Myung-A; Jin, Dong-Kyu; Lee, Namho; Kim, Byung Jin; Koh, Kwang Kon; Suh, Jon; Lee, Seung-Hwan; Lee, Byoung-Kwon; Oh, Seung-Jin; Jin, Han-Young; Ahn, Youngkeun; Lee, Sang-Gon; Bae, Jang-Ho; Park, Woo Jung; Lee, Sang-Chol; Lee, Han Cheol; Lee, Jaewon; Park, Cheolwon; Lee, Backhwan; Jang, Yangsoo.
Afiliação
  • Yang YJ; Division of Cardiology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea; Cardiovascular Research Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Lee SH; Division of Cardiology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea; Cardiovascular Research Institute, Yonsei University College of Medicine, Seoul, Korea. Electronic address: shl1106@yuhs.ac.
  • Kim BS; Division of Cardiology, Department of Internal Medicine, Daedong Hospital, Busan, Korea.
  • Cho YK; Division of Cardiology, Keimyung University Dongsan Medical Center, Daegu, Korea.
  • Cho HJ; Cardiovascular Center and Cardiovascular Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Cho KI; Division of Cardiology, Department of Internal Medicine, Cardiovascular Research Institute, Kosin University School of Medicine, Busan, Korea.
  • Kim SY; Department of Cardiology, Seoul Medical Center, Seoul, Korea.
  • Ryu JK; Department of Cardiology, Daegu Catholic University Medical Center, Daegu, Korea.
  • Cho JM; Department of Cardiology, Kyunghee University East-West Neo Medical Center, Seoul, Korea.
  • Park JI; Division of Cardiology, Department of Internal Medicine, Veterans Health Service Medical Center, Seoul, Korea.
  • Park JS; Department of Medicine, Yeungnam University Medical Center, Daegu, Korea.
  • Park CG; Department of Cardiology, Korea University Guro Hospital, Seoul, Korea.
  • Chun WJ; Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
  • Kim MA; Division of Cardiology, Department of Internal Medicine, SMG-SNU Seoul Boramae Hospital, Seoul, Korea.
  • Jin DK; Division of Cardiology, Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Korea.
  • Lee N; Cardiology Division, Kangnam Sacred Heart Hospital, Hallym University Medical Center, Seoul, Korea.
  • Kim BJ; Division of Cardiology, Department of Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Koh KK; Department of Cardiology, Gachon University Gil Medical Center, Incheon, Korea.
  • Suh J; Department of Cardiology, Soonchunhyang University Hospital Bucheon, Bucheon, Korea.
  • Lee SH; Division of Cardiology, Wonju College of Medicine, Yonsei University, Wonju, Korea.
  • Lee BK; Division of Cardiology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
  • Oh SJ; Division of Cardiology, Department of Internal Medicine, NHIS Ilsan Hospital, Goyang, Korea.
  • Jin HY; Division of Cardiology, Department of Internal Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Ahn Y; Department of Cardiology, Heart Research Center of Chonnam National University, Gwangju, Korea.
  • Lee SG; Department of Cardiology, Ulsan University College of Medicine, Ulsan, Korea.
  • Bae JH; Division of Cardiology, Department of Internal Medicine, Konyang University Hospital, Daejeon, Korea.
  • Park WJ; Division of Cardiology, Department of Internal Medicine, Hallym University Medical Center, Anyang, Korea.
  • Lee SC; Division of Cardiology, Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Lee HC; Division of Cardiology, Department of Internal Medicine, Pusan National University School of Medicine, Medical Research Institute, Pusan National University Hospital, Busan, Korea.
  • Lee J; Research & Development Division, Alvogen Korea Co., Ltd., Seoul, Korea.
  • Park C; Research & Development Division, Alvogen Korea Co., Ltd., Seoul, Korea.
  • Lee B; Research & Development Division, Alvogen Korea Co., Ltd., Seoul, Korea.
  • Jang Y; Division of Cardiology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea; Cardiovascular Research Institute, Yonsei University College of Medicine, Seoul, Korea. Electronic address: jangys1212@yuhs.ac.
Clin Ther ; 39(1): 107-117, 2017 Jan.
Article em En | MEDLINE | ID: mdl-28007331
ABSTRACT

PURPOSE:

The aim of this study was to evaluate the efficacy and tolerability of rosuvastatin/ezetimibe combination therapy in Korean patients with high cardiovascular risk.

METHODS:

This was a 12-week, randomized, double-blind, placebo-controlled, multicenter study. A total of 337 patients were screened. After a 4-week run-in period, 245 of these patients with high or moderately high risk as defined by the National Cholesterol Education Program Adult Treatment Panel III guidelines were randomly assigned. Patients received 1 of 6 regimens for 8 weeks as follows (1) rosuvastatin 5 mg, (2) rosuvastatin 5 mg/ezetimibe 10 mg, (3) rosuvastatin 10 mg, (4) rosuvastatin 10 mg/ezetimibe 10 mg, (5) rosuvastatin 20 mg, or (6) rosuvastatin 20 mg/ezetimibe 10 mg. The primary outcome variable was percentage change in the level of LDL-C at week 8 of drug treatment. Secondary outcome variables included percentage changes of other lipid variables and achievement rates of LDL-C targets. Tolerability analyses were also performed.

FINDINGS:

The percentage change of LDL-C ranged from -45% to -56% (mean, -51%) in the monotherapy groups and from -58% to -63% (mean, -60%) in the combination therapy groups. The percentage change was greater in the pooled combination therapy group than in the counterpart (P < 0.001 for the pooled groups); this difference was more obvious for regimens with a lower statin dose. The percentage reductions of total cholesterol and triglycerides were greater in the combination groups than in the monotherapy groups. The LDL-C target achievement rates were 64% to 87% (mean, 73%) in the monotherapy groups and 87% to 95% (mean, 91%) in the combination groups (P = 0.01 for the pooled groups). The rates were significantly greater in patients receiving the combination therapy than in the monotherapy at lower doses of rosuvastatin. The proportions of patients with various adverse events were not significantly different between the groups. IMPLICATIONS Rosuvastatin/ezetimibe combination therapy has better efficacy and target achievement rates than rosuvastatin monotherapy in patients with high cardiovascular risk.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rosuvastatina Cálcica / Ezetimiba / Hipercolesterolemia / Anticolesterolemiantes Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Ther Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rosuvastatina Cálcica / Ezetimiba / Hipercolesterolemia / Anticolesterolemiantes Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Ther Ano de publicação: 2017 Tipo de documento: Article