Evidence map›Paper›PMID 41738355›Full record

ArticleEuropean heart journal. Cardiovascular Imaging2026

Achieved LDL-C levels <55 mg/dL and cardiac events in patients and lesions harbouring lipid-rich plaque phenotypes.

Yu Kataoka, Stephen J Nicholls, Eri Kiyoshige, Kunihiro Nishimura, Rishi Puri, Satoshi Kitahara, Kota Murai, Kentaro Mitsui, Yoshiyuki Tomishima, Kenichiro Sawada and 12 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in European heart journal. Cardiovascular Imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04864171 (REvelation of PAthophySiological PhenotypeS of VUlneRable Lipid-Rich PlaquE on Near-InfraRed Spectroscopy), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

NCT04864171 recruitingnot on this map

REvelation of PAthophySiological PhenotypeS of VUlneRable Lipid-Rich PlaquE on Near-InfraRed Spectroscopy: REASSURE-NIRS

Typeobservational_patient_registrySponsorNational Cerebral and Cardiovascular Center, JapanRan2018 to 2030Enrolled2,000ConditionsLipid-Rich Atherosclerosis of Coronary ArteryArmsnear-infrared spectroscopy
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Yu KataokaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.ORCID 0000-0001-6307-5593
Stephen J NichollsMonash Heart, Monash University, Clayton, Victoria, Australia.
Eri KiyoshigeDepartment of Preventive Cardiology, National Cerebral & Cardiovascular Center, Suita, Osaka, Japan.
Kunihiro NishimuraDepartment of Preventive Cardiology, National Cerebral & Cardiovascular Center, Suita, Osaka, Japan.
Rishi PuriDepartment of Cardiovascular Medicine, Cleveland Clinic, Cleveland, OH, USA.ORCID 0000-0001-8849-7426
Satoshi KitaharaDepartment of Cardiology, Kashiwa Kosei General Hospital, Kashiwa, Chiba, Japan.ORCID 0000-0002-6073-1302
Kota MuraiDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.ORCID 0000-0002-5162-4783
Kentaro MitsuiDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Yoshiyuki TomishimaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Kenichiro SawadaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Hideo MatamaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Takamasa IwaiDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Satoshi HondaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Kazuhiro NakaoDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Masashi FujinoDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.ORCID 0000-0002-2706-4317
Kensuke TakagiDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Shuichi YonedaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Fumiyuki OtsukaDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.
Kensaku NishihiraDepartment of Cardiology, Miyazaki Medical Association Hospital, Miyazaki, Japan.ORCID 0000-0002-1718-3830
Itaru TakamisawaDepartment of Cardiovascular Medicine, Sakakibara Heart Institute, Fuchu, Tokyo, Japan.
Yasuhide AsaumiDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.ORCID 0000-0002-9009-7234
Teruo NoguchiDepartment of Cardiovascular Medicine, National Cerebral & Cardiovascular Center, 6-1 Kishibe-shinmachi, Suita, Osaka 5648565, Japan.ORCID 0000-0001-5372-4932

Funding

Advancement of Measuring Technologies in Biomedical EngineeringFukuda Foundation for Medical TechnologyNakatani Foundation
6 · The paper itself

Abstract

aimsThe European Society of Cardiology guidelines recommend low-density lipoprotein cholesterol (LDL-C) < 55 mg/dL in very-high-risk patients. Given that plaque phenotype underscores its modulatory response to lipid-lowering therapies, patients and lesions harbouring lipid-laden plaques may benefit from LDL-C < 55 mg/dL to reduce their cardiovascular risks. METHODS AND

resultsThe REASSURE-NIRS (REvelation of PAthophySiological PhenotypeS of VUlneRable Lipid-Rich PlaquE on Near-InfraRed Spectroscopy) multi-centre registry enrolled 853 coronary artery disease patients (non-culprit lesions = 1662) receiving NIRS/IVUS-guided PCI (NCT04864171). LDL-C level at 3 months after PCI was used as on-treatment LDL-C. Study subjects were stratified according to maxLCBI4mm at non-culprit lesions < vs. ≥324.7. In each group, major adverse cardiac events (MACE) (=cardiac-cause death + non-fatal myocardial infarction (MI) + ischaemia-driven non-culprit lesion revascularization) was compared in those with on-treatment LDL-C < vs. ≥55 mg/dL. 31.6% of study subjects achieved on-treatment LDL-C < 55 mg/dL. During the observational period (median = 1109 days), MACE rate did not differ in patients with maxLCBI4mm < 324.7 exhibiting on-treatment LDL-C levels < and ≥55 mg/dL [adjusted hazard ratio (HR) = 1.42, 95% confidence interval (CI) = 0.80-2.54, P = 0.227]. By contrast, in patients with non-culprit lesion maxLCBI4mm ≥ 324.7, a significantly reduced MACE rate was observed in those with on-treatment LDL-C < 55 mg/dL (adjusted HR = 0.23, 95% CI: 0.09-0.57, P = 0.010). These relationships were similarly observed in a lesion-based analysis (non-culprit lesion maxLCBI4mm < 324.7: adjusted HR = 1.30, 95% CI = 0.42-4.00, P = 0.640, non-culprit lesion maxLCBI4mm ≥ 324.7: adjusted HR = 0.27, 95% CI:0.08-0.97, P = 0.045). Notably, in patients with multiple non-culprit lesions with maxLCBI4mm ≥ 324.7, on-treatment LDL-C < 55 mg/dL was associated with a lower frequency of MACE (adjusted HR = 0.22, 95% CI = 0.09-0.53, P < 0.001), whereas this relationship was not observed in those with single non-culprit lesion with maxLCBI4mm ≥ 324.7 (adjusted HR = 0.03, 95% CI = 0.00-5.55, P = 0.196).

conclusionNIRS-derived lipid-rich plaque may be a potential imaging measure reflecting patients and lesions that may benefit from achieving LDL-C levels < 55 mg/dL.

Indexed as

Cholesterol, LDLCoronary Artery DiseasePercutaneous Coronary InterventionPlaque, AtheroscleroticAgedCohort StudiesCoronary AngiographyFemaleHumansMaleMiddle AgedPhenotypeRegistriesRisk AssessmentSpectroscopy, Near-InfraredTreatment OutcomeCholesterol, LDLguidelinelipid-rich plaquelow-density lipoprotein cholesterolnear-infrared spectroscopy

Identifiers

PMID41738355
PMCPMC13128272

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