Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/58081
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dc.contributor.authorKataoka Y.-
dc.contributor.authorNicholls S.J.-
dc.contributor.authorKitahara S.-
dc.contributor.authorKatasako-Yabumoto A.-
dc.contributor.authorHosoda H.-
dc.contributor.authorFunabashi S.-
dc.contributor.authorMitsui K.-
dc.contributor.authorMurai K.-
dc.contributor.authorIwai T.-
dc.contributor.authorSawada K.-
dc.contributor.authorMatama H.-
dc.contributor.authorHonda S.-
dc.contributor.authorTakagi K.-
dc.contributor.authorFujino M.-
dc.contributor.authorYoneda S.-
dc.contributor.authorOtsuka F.-
dc.contributor.authorNakao K.-
dc.contributor.authorAsaumi Y.-
dc.contributor.authorNoguchi T.-
dc.date.accessioned2026-04-26T23:40:46Z-
dc.date.available2026-04-26T23:40:46Z-
dc.date.copyright2026-
dc.date.issued2026-04-09en
dc.identifier.citationAtherosclerosis. 415(no pagination), 2026. Article Number: 120684. Date of Publication: 01 Apr 2026.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/58081-
dc.description.abstractBACKGROUND AND AIMS: The ESC guideline recommends LDL-C<1.0 mmol/L in extreme-risk patients. However, recent clinical trials demonstrated cardiovascular benefits with achieving very low LDL-C levels even in very high-risk patients including patients with CAD. Patients with CAD may more benefit from lowering LDL-C<1.0 mmol/L rather than their guideline-recommended LDL-C goal (<1.4 mmol/L). METHOD(S): The current multi-center observational study analyzed 2560 patients with CAD receiving PCI (2017.1.1-2022.8.31). All of study participants were clinically followed for at least three years after PCI. The primary (cardiac death, non-fatal MI and clinically-driven coronary revascularization at non-culprit segments) and secondary outcomes (cardiac death, non-fatal MI) were compared in those stratified according to on-treatment LDL-C levels at 2 months after PCI (<1.0, 1.0-1.3 and >= 1.4 mmol/L). RESULT(S): On-treatment LDL-C<1.0 mmol/L was achieved in 9.8% (=251/2560) of study participants. In extreme-risk patients exhibiting the concomitance of polyvascular disease or a history of recurrent ASCVD, the proportions of LDL-C<1.0 mmol/L were 10.5 and 9.6%, respectively. More intensified lipid-lowering therapies were used in those with on-treatment LDL-C<1.0 mmol/L (high-intensity statin = 77.7%, p < 0.001; ezetimibe = 67.3%, p < 0.001; PCSK9-I = 13.9%, p < 0.001). During the observational perid (median = 1882 days), achieving on-treatment LDL-C<1.0 mmol/L significantly reduced risks of primary (adjusted HR = 0.23, 95%CI = 0.11-0.48, p < 0.001) and secondary outcomes (adjusted HR = 0.31, 95%CI = 0.11-0.84, p = 0.022). These benefits were consistently observed regardless of age, gender, types of CAD and various traditional risk factors. CONCLUSION(S): Achieving LDL-C<1.0 mmol/L mitigated risks of subsequent atherosclerotic cardiovascular events in patients with CAD. More actions are needed to further promote the intensification of lipid-lowering therapies in patients with CAD.Copyright © 2026 The Authors. Published by Elsevier B.V. All rights reserved.-
dc.relation.ispartofAtherosclerosis-
dc.titleAchieving LDL-C <1.0 mmol/L and cardiovascular outcomes in patients with coronary artery disease who received percutaneous coronary intervention.-
dc.typeArticle In Press-
dc.identifier.affiliationCardiology (MonashHeart)-
dc.identifier.doihttps://dx.doi.org/10.1016/j.atherosclerosis.2026.120684-
dc.publisher.placeIreland-
dc.identifier.pubmedid41916797-
dc.identifier.institution(Kataoka, Katasako-Yabumoto, Mitsui, Murai, Iwai, Sawada, Matama, Honda, Takagi, Fujino, Yoneda, Otsuka, Nakao, Asaumi, Noguchi) Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan-
dc.identifier.institution(Nicholls) Victorian Heart Institute (VHI), Medicine Monash Health, Clayton, Australia-
dc.identifier.institution(Kitahara) Department of Cardiovascular Medicine, Kashiwa Kousei General Hospital, Kashiwa, Japan-
dc.identifier.institution(Hosoda) Department of Cardiovascular Medicine, Chikamori hospital, Japan-
dc.identifier.institution(Funabashi) Department of Cardiovascular Medicine, Kyorin University, Mitaka, Tokyo, Japan-
dc.identifier.affiliationmh(Nicholls) Victorian Heart Institute (VHI), Medicine Monash Health, Clayton, Australia-
item.fulltextNo Fulltext-
item.openairetypeArticle In Press-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
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