0 71

Cited 0 times in

Cited 1 times in

Remnant cholesterol as a residual risk in atherosclerotic cardiovascular disease patients under statin-based lipid-lowering therapy: A post hoc analysis of the RACING trial

DC Field Value Language
dc.contributor.author고영국-
dc.contributor.author김병극-
dc.contributor.author김중선-
dc.contributor.author안철민-
dc.contributor.author이승준-
dc.contributor.author이용준-
dc.contributor.author장양수-
dc.contributor.author최동훈-
dc.contributor.author홍명기-
dc.contributor.author홍성진-
dc.date.accessioned2025-04-17T08:27:18Z-
dc.date.available2025-04-17T08:27:18Z-
dc.date.issued2024-11-
dc.identifier.issn1933-2874-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/204617-
dc.description.abstractBackground: Remnant cholesterol (remnant-C) levels during lipid-lowering therapy (LLT) may indicate residual risk. Objective: We aimed to investigate the clinical outcomes based on on-treatment remnant-C distribution in patients with atherosclerotic cardiovascular disease (ASCVD) under statin-based LLT. Methods: In this post hoc analysis of the RACING trial, 3,348 patients with ASCVD lipid profiles 1 year after randomization were investigated. Remnant-C was calculated as total cholesterol minus low-density lipoprotein cholesterol (LDL-C) minus high-density lipoprotein cholesterol. The primary endpoint was a 3-year composite of cardiovascular death, major cardiovascular events, or non-fatal stroke. Results: The study population was grouped into tertiles according to on-treatment remnant-C: high (> 20.5 mg/dL; n = 1,116), intermediate (14‒20.5 mg/dL; n = 1,031), and low (≤14.0 mg/dL; n = 1,201) remnant-C groups. The high remnant-C group showed the highest incidence of the primary endpoint at 3 years (11.0%, 10.3%, and 7.5% in the high, intermediate, and low remnant-C groups, respectively; p = 0.009). The high remnant-C levels at 1 year were independently associated with an increased risk of the primary outcome, whereas achieving LDL-C < 55 or 70 mg/dL was not associated with the incidence of the primary endpoint. The on-treatment remnant-C cut-off of 17 mg/dL (median) demonstrated the ability to discriminate between patients at higher and lower risks for the primary endpoints (hazard ratio: 1.42; 95% confidence interval: 1.14‒1.78; p = 0.002). Conclusions: In patients with ASCVD undergoing statin-based LLT, high on-treatment remnant-C values were associated with unfavorable clinical outcomes. On-treatment remnant-C levels may serve as an additional means of assessing residual cardiovascular risk. Clinical trial registration: ClinicalTrials. gov ID: NCT03044665.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfJOURNAL OF CLINICAL LIPIDOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAged-
dc.subject.MESHAtherosclerosis* / blood-
dc.subject.MESHAtherosclerosis* / drug therapy-
dc.subject.MESHCardiovascular Diseases / blood-
dc.subject.MESHCardiovascular Diseases / drug therapy-
dc.subject.MESHCholesterol* / blood-
dc.subject.MESHCholesterol, LDL / blood-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors* / therapeutic use-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRisk Factors-
dc.titleRemnant cholesterol as a residual risk in atherosclerotic cardiovascular disease patients under statin-based lipid-lowering therapy: A post hoc analysis of the RACING trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorJung-Hee Lee-
dc.contributor.googleauthorSung Gyun Ahn-
dc.contributor.googleauthorHo Sung Jeon-
dc.contributor.googleauthorJun-Won Lee-
dc.contributor.googleauthorYoung Jin Youn-
dc.contributor.googleauthorYong-Joon Lee-
dc.contributor.googleauthorSeung-Jun Lee-
dc.contributor.googleauthorSung-Jin Hong-
dc.contributor.googleauthorChul-Min Ahn-
dc.contributor.googleauthorYoung-Guk Ko-
dc.contributor.googleauthorJung-Sun Kim-
dc.contributor.googleauthorDonghoon Choi-
dc.contributor.googleauthorMyeong-Ki Hong-
dc.contributor.googleauthorYangsoo Jang-
dc.contributor.googleauthorByeong-Keuk Kim-
dc.identifier.doi10.1016/j.jacl.2024.07.005-
dc.contributor.localIdA00127-
dc.contributor.localIdA00493-
dc.contributor.localIdA00961-
dc.contributor.localIdA02269-
dc.contributor.localIdA02927-
dc.contributor.localIdA02984-
dc.contributor.localIdA03448-
dc.contributor.localIdA04053-
dc.contributor.localIdA04391-
dc.contributor.localIdA04403-
dc.relation.journalcodeJ01324-
dc.identifier.pmid39322526-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1933287424002101-
dc.subject.keywordAtherosclerotic cardiovascular disease-
dc.subject.keywordEzetimibe-
dc.subject.keywordRemnant cholesterol-
dc.subject.keywordStatin-
dc.contributor.alternativeNameKo, Young Guk-
dc.contributor.affiliatedAuthor고영국-
dc.contributor.affiliatedAuthor김병극-
dc.contributor.affiliatedAuthor김중선-
dc.contributor.affiliatedAuthor안철민-
dc.contributor.affiliatedAuthor이승준-
dc.contributor.affiliatedAuthor이용준-
dc.contributor.affiliatedAuthor장양수-
dc.contributor.affiliatedAuthor최동훈-
dc.contributor.affiliatedAuthor홍명기-
dc.contributor.affiliatedAuthor홍성진-
dc.citation.volume18-
dc.citation.number6-
dc.citation.startPagee905-
dc.citation.endPagee914-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL LIPIDOLOGY, Vol.18(6) : e905-e914, 2024-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.