Evidence mapPaperPMID 28007331Full record

Trial reportClinical therapeutics2017

Combination Therapy of Rosuvastatin and Ezetimibe in Patients with High Cardiovascular Risk.

Young-June Yang, Sang-Hak Lee, Byung Soo Kim, Yun-Kyeong Cho, Hyun-Jai Cho, Kyoung Im Cho, Seok-Yeon Kim, Jae Kean Ryu, Jin-Man Cho, Joong-Il Park and 23 more

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Clinical therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04826354 (Effects of High-dose StAtin Versus Low-dose Statin Plus Ezetimibe on Statin-Associated Muscle Symptoms & on Reaching Target LDL-C Levels Among Elderly Patients With Atherosclerotic Cardiovascular Disease), which is not on this map. Cited by 27 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 5 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04826354 phase4completedstarted 2021, after this paper: background citation

Effects of High-dose StAtin Versus Low-dose Statin Plus Ezetimibe on Statin-Associated Muscle Symptoms & on Reaching Target LDL-C Levels Among Elderly Patients With Atherosclerotic Cardiovascular Disease

Ran2021Enrolled582Registered outcomes11Posted comparisons0ConditionsAtheroscleroses, CoronaryArmsRosuvastatin, rosuvastatin and ezetimibe
Open the trial in the graph
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
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  20. Is it Time for Single-Pill Combinations in Dyslipidemia?American journal of cardiovascular drugs : drugs, devices, and other interventions · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

33 authors.

Young-June YangDivision 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.
Sang-Hak LeeDivision 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.
Byung Soo KimDivision of Cardiology, Department of Internal Medicine, Daedong Hospital, Busan, Korea.
Yun-Kyeong ChoDivision of Cardiology, Keimyung University Dongsan Medical Center, Daegu, Korea.
Hyun-Jai ChoCardiovascular Center and Cardiovascular Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Kyoung Im ChoDivision of Cardiology, Department of Internal Medicine, Cardiovascular Research Institute, Kosin University School of Medicine, Busan, Korea.
Seok-Yeon KimDepartment of Cardiology, Seoul Medical Center, Seoul, Korea.
Jae Kean RyuDepartment of Cardiology, Daegu Catholic University Medical Center, Daegu, Korea.
Jin-Man ChoDepartment of Cardiology, Kyunghee University East-West Neo Medical Center, Seoul, Korea.
Joong-Il ParkDivision of Cardiology, Department of Internal Medicine, Veterans Health Service Medical Center, Seoul, Korea.
Jong-Seon ParkDepartment of Medicine, Yeungnam University Medical Center, Daegu, Korea.
Chang Gyu ParkDepartment of Cardiology, Korea University Guro Hospital, Seoul, Korea.
Woo Jung ChunSamsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
Myung-A KimDivision of Cardiology, Department of Internal Medicine, SMG-SNU Seoul Boramae Hospital, Seoul, Korea.
Dong-Kyu JinDivision of Cardiology, Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Korea.
Namho LeeCardiology Division, Kangnam Sacred Heart Hospital, Hallym University Medical Center, Seoul, Korea.
Byung Jin KimDivision of Cardiology, Department of Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Kwang Kon KohDepartment of Cardiology, Gachon University Gil Medical Center, Incheon, Korea.
Jon SuhDepartment of Cardiology, Soonchunhyang University Hospital Bucheon, Bucheon, Korea.
Seung-Hwan LeeDivision of Cardiology, Wonju College of Medicine, Yonsei University, Wonju, Korea.
Byoung-Kwon LeeDivision of Cardiology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Seung-Jin OhDivision of Cardiology, Department of Internal Medicine, NHIS Ilsan Hospital, Goyang, Korea.
Han-Young JinDivision of Cardiology, Department of Internal Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
Youngkeun AhnDepartment of Cardiology, Heart Research Center of Chonnam National University, Gwangju, Korea.
Sang-Gon LeeDepartment of Cardiology, Ulsan University College of Medicine, Ulsan, Korea.
Jang-Ho BaeDivision of Cardiology, Department of Internal Medicine, Konyang University Hospital, Daejeon, Korea.
Woo Jung ParkDivision of Cardiology, Department of Internal Medicine, Hallym University Medical Center, Anyang, Korea.
Sang-Chol LeeDivision of Cardiology, Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Han Cheol LeeDivision of Cardiology, Department of Internal Medicine, Pusan National University School of Medicine, Medical Research Institute, Pusan National University Hospital, Busan, Korea.
Jaewon LeeResearch & Development Division, Alvogen Korea Co., Ltd., Seoul, Korea.
Cheolwon ParkResearch & Development Division, Alvogen Korea Co., Ltd., Seoul, Korea.
Backhwan LeeResearch & Development Division, Alvogen Korea Co., Ltd., Seoul, Korea.
Yangsoo JangDivision 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.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

methodsThis 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.

findingsThe 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.

Indexed as

AgedAnticholesteremic AgentsCardiovascular DiseasesCholesterolDouble-Blind MethodDrug Therapy, CombinationEzetimibeFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHypercholesterolemiaMaleMiddle AgedRisk FactorsRosuvastatin CalciumTreatment OutcomeAnticholesteremic AgentsCholesterolEzetimibeHydroxymethylglutaryl-CoA Reductase InhibitorsRosuvastatin CalciumTriglyceridescardiovascular diseasescholesteroldrug combinationsezetimibeLDLrosuvastatin calcium

Identifiers

What Socratic holds

Texttitle and abstract
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.