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https://repository.monashhealth.org/monashhealthjspui/handle/1/58081Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kataoka Y. | - |
| dc.contributor.author | Nicholls S.J. | - |
| dc.contributor.author | Kitahara S. | - |
| dc.contributor.author | Katasako-Yabumoto A. | - |
| dc.contributor.author | Hosoda H. | - |
| dc.contributor.author | Funabashi S. | - |
| dc.contributor.author | Mitsui K. | - |
| dc.contributor.author | Murai K. | - |
| dc.contributor.author | Iwai T. | - |
| dc.contributor.author | Sawada K. | - |
| dc.contributor.author | Matama H. | - |
| dc.contributor.author | Honda S. | - |
| dc.contributor.author | Takagi K. | - |
| dc.contributor.author | Fujino M. | - |
| dc.contributor.author | Yoneda S. | - |
| dc.contributor.author | Otsuka F. | - |
| dc.contributor.author | Nakao K. | - |
| dc.contributor.author | Asaumi Y. | - |
| dc.contributor.author | Noguchi T. | - |
| dc.date.accessioned | 2026-04-26T23:40:46Z | - |
| dc.date.available | 2026-04-26T23:40:46Z | - |
| dc.date.copyright | 2026 | - |
| dc.date.issued | 2026-04-09 | en |
| dc.identifier.citation | Atherosclerosis. 415(no pagination), 2026. Article Number: 120684. Date of Publication: 01 Apr 2026. | - |
| dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/58081 | - |
| dc.description.abstract | BACKGROUND 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.ispartof | Atherosclerosis | - |
| dc.title | Achieving LDL-C <1.0 mmol/L and cardiovascular outcomes in patients with coronary artery disease who received percutaneous coronary intervention. | - |
| dc.type | Article In Press | - |
| dc.identifier.affiliation | Cardiology (MonashHeart) | - |
| dc.identifier.doi | https://dx.doi.org/10.1016/j.atherosclerosis.2026.120684 | - |
| dc.publisher.place | Ireland | - |
| dc.identifier.pubmedid | 41916797 | - |
| 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.fulltext | No Fulltext | - |
| item.openairetype | Article In Press | - |
| item.cerifentitytype | Publications | - |
| item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
| item.grantfulltext | none | - |
| crisitem.author.dept | Cardiology (MonashHeart & Victorian Heart Institute) | - |
| Appears in Collections: | Articles | |
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