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Intensive LDL Cholesterol Targeting in Atherosclerotic Cardiovascular Disease

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dc.contributor.authorLee, Yong-Joon-
dc.contributor.authorLee, Seung-Jun-
dc.contributor.authorKim, Jin Won-
dc.contributor.authorLee, Sang-Hyup-
dc.contributor.authorKim, Gwang-Sil-
dc.contributor.authorPark, Jae Hyoung-
dc.contributor.authorCho, Jin-Man-
dc.contributor.authorKang, Woong Chol-
dc.contributor.authorYoon, Hyuck-Jun-
dc.contributor.authorKim, Won Ho-
dc.contributor.authorLee, Seung-Jin-
dc.contributor.authorLee, Jin Bae-
dc.contributor.authorJang, Ji-Yong-
dc.contributor.authorShin, Sanghoon-
dc.contributor.authorPark, Ik Hyun-
dc.contributor.authorKwon, Sung Uk-
dc.contributor.authorKim, Sunwon-
dc.contributor.authorHong, Sung-Jin-
dc.contributor.authorAhn, Chul-Min-
dc.contributor.authorKim, Jung-Sun-
dc.contributor.authorKo, Young-Guk-
dc.contributor.authorChoi, Donghoon-
dc.contributor.authorHong, Myeong-Ki-
dc.contributor.authorJang, Yangsoo-
dc.contributor.authorKim, Byeong-Keuk-
dc.date.accessioned2026-04-13T08:36:59Z-
dc.date.available2026-04-13T08:36:59Z-
dc.date.created2026-04-10-
dc.date.issued2026-04-
dc.identifier.issn0028-4793-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/211823-
dc.description.abstractBackground Despite guideline recommendations, evidence from randomized trials evaluating the appropriate low-density lipoprotein (LDL) cholesterol target for secondary prevention in patients with atherosclerotic cardiovascular disease remains limited.Methods In this open-label superiority trial conducted in South Korea, we randomly assigned patients with atherosclerotic cardiovascular disease in a 1:1 ratio to a target LDL cholesterol level of less than 55 mg per deciliter (1.4 mmol per liter) (intensive-targeting group) or less than 70 mg per deciliter (1.8 mmol per liter) (conventional-targeting group). The primary end point was a composite of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, any revascularization, or hospitalization for unstable angina at 3 years. Safety was also assessed.Results Of 3048 patients who underwent randomization, 1526 were assigned to the intensive-targeting group and 1522 to the conventional-targeting group. The median follow-up was 3.0 years. The median LDL cholesterol level during the trial was 56 mg per deciliter (1.4 mmol per liter) in the intensive-targeting group and 66 mg per deciliter (1.7 mmol per liter) in the conventional-targeting group. A primary end-point event occurred in 100 patients (Kaplan-Meier estimate of cumulative incidence, 6.6%) in the intensive-targeting group and in 147 patients (Kaplan-Meier estimate of cumulative incidence, 9.7%) in the conventional-targeting group (hazard ratio, 0.67; 95% confidence interval, 0.52 to 0.86; P=0.002). The incidence of prespecified safety end points was similar in the two trial groups, except for a lower incidence of creatinine elevation in the intensive-targeting group.Conclusions Among patients with atherosclerotic cardiovascular disease, targeting an LDL cholesterol level of less than 55 mg per deciliter resulted in a lower risk of cardiovascular events at 3 years than targeting a level of less than 70 mg per deciliter. (Funded by the Cardiovascular Research Center and Yuhan; Ez-PAVE ClinicalTrials.gov number, NCT04626973.) Among patients with atherosclerotic cardiovascular disease, targeting an LDL cholesterol level below 55 mg per deciliter led to a lower 3-year risk of cardiovascular events than targeting a level below 70 mg per deciliter.-
dc.languageEnglish-
dc.publisherMassachusetts Medical Society-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.subject.MESHAged-
dc.subject.MESHAnticholesteremic Agents* / administration & dosage-
dc.subject.MESHAnticholesteremic Agents* / adverse effects-
dc.subject.MESHAnticholesteremic Agents* / therapeutic use-
dc.subject.MESHAtherosclerosis* / blood-
dc.subject.MESHAtherosclerosis* / drug therapy-
dc.subject.MESHAtherosclerosis* / mortality-
dc.subject.MESHCardiovascular Diseases* / mortality-
dc.subject.MESHCardiovascular Diseases* / prevention & control-
dc.subject.MESHCholesterol, LDL* / blood-
dc.subject.MESHFemale-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHHospitalization / statistics & numerical data-
dc.subject.MESHHumans-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors* / adverse effects-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors* / therapeutic use-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHSecondary Prevention* / methods-
dc.titleIntensive LDL Cholesterol Targeting in Atherosclerotic Cardiovascular Disease-
dc.typeArticle-
dc.contributor.googleauthorLee, Yong-Joon-
dc.contributor.googleauthorLee, Seung-Jun-
dc.contributor.googleauthorKim, Jin Won-
dc.contributor.googleauthorLee, Sang-Hyup-
dc.contributor.googleauthorKim, Gwang-Sil-
dc.contributor.googleauthorPark, Jae Hyoung-
dc.contributor.googleauthorCho, Jin-Man-
dc.contributor.googleauthorKang, Woong Chol-
dc.contributor.googleauthorYoon, Hyuck-Jun-
dc.contributor.googleauthorKim, Won Ho-
dc.contributor.googleauthorLee, Seung-Jin-
dc.contributor.googleauthorLee, Jin Bae-
dc.contributor.googleauthorJang, Ji-Yong-
dc.contributor.googleauthorShin, Sanghoon-
dc.contributor.googleauthorPark, Ik Hyun-
dc.contributor.googleauthorKwon, Sung Uk-
dc.contributor.googleauthorKim, Sunwon-
dc.contributor.googleauthorHong, Sung-Jin-
dc.contributor.googleauthorAhn, Chul-Min-
dc.contributor.googleauthorKim, Jung-Sun-
dc.contributor.googleauthorKo, Young-Guk-
dc.contributor.googleauthorChoi, Donghoon-
dc.contributor.googleauthorHong, Myeong-Ki-
dc.contributor.googleauthorJang, Yangsoo-
dc.contributor.googleauthorKim, Byeong-Keuk-
dc.identifier.doi10.1056/NEJMoa2600283-
dc.relation.journalcodeJ02371-
dc.identifier.eissn1533-4406-
dc.identifier.pmid41910315-
dc.identifier.urlhttps://www.nejm.org/doi/10.1056/NEJMoa2600283-
dc.contributor.affiliatedAuthorLee, Yong-Joon-
dc.contributor.affiliatedAuthorLee, Seung-Jun-
dc.contributor.affiliatedAuthorLee, Sang-Hyup-
dc.contributor.affiliatedAuthorAhn, Chul-Min-
dc.contributor.affiliatedAuthorKim, Jung-Sun-
dc.contributor.affiliatedAuthorKo, Young-Guk-
dc.contributor.affiliatedAuthorChoi, Donghoon-
dc.contributor.affiliatedAuthorHong, Myeong-Ki-
dc.contributor.affiliatedAuthorJang, Yangsoo-
dc.contributor.affiliatedAuthorKim, Byeong-Keuk-
dc.identifier.wosid001726645800001-
dc.citation.volume394-
dc.citation.number14-
dc.citation.startPage1365-
dc.citation.endPage1375-
dc.identifier.bibliographicCitationNEW ENGLAND JOURNAL OF MEDICINE, Vol.394(14) : 1365-1375, 2026-04-
dc.identifier.rimsid92391-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordPlusSTATIN THERAPY-
dc.subject.keywordPlusATORVASTATIN-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusEZETIMIBE-
dc.subject.keywordPlusOUTCOMES-
dc.subject.keywordPlusIMPACT-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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