Impact of LR11 as Residual Risk on Long-Term Clinical Outcomes in Patients with Coronary Artery Disease Treated with Statins after First Percutaneous Coronary Intervention.


Journal

International heart journal
ISSN: 1349-3299
Titre abrégé: Int Heart J
Pays: Japan
ID NLM: 101244240

Informations de publication

Date de publication:
30 May 2020
Historique:
pubmed: 1 5 2020
medline: 6 6 2020
entrez: 1 5 2020
Statut: ppublish

Résumé

Cardiovascular events still occur despite statin-based lipid-lowering therapy in patients with coronary artery disease (CAD). LR11, a member of the low-density lipoprotein receptor family, is a novel marker for the proliferation of intimal smooth muscle cells, which are critical to atherosclerotic plaque formation. We evaluated the impact of LR11 on long-term clinical outcomes in CAD patients treated with statins after percutaneous coronary intervention (PCI).This study included 223 consecutive CAD patients (age, 64.5 ± 9.6 years; male, 81.2%) treated with statin after first PCI between March 2003 and December 2004 at our institution. Patients were stratified to two groups according to LR11 levels (median). Composite cardiovascular disease (CVD) endpoints that included cardiovascular death, non-fatal acute coronary syndrome and non-fatal stroke were compared between groups.The rate of CVD endpoints was significantly higher in the high LR11 group (log-rank, P = 0.0029) during the median follow-up period of 2844 days. Multivariate Cox regression analysis showed that a higher LR11 level was significantly associated with adverse clinical outcomes (adjusted hazard ratio for composite CVD endpoints, 2.47; 95% confidence interval, 1.29-4.92; P = 0.006).Elevated levels of LR11 were significantly associated with long-term clinical outcomes among CAD patients treated with statins after first PCI.

Identifiants

pubmed: 32350212
doi: 10.1536/ihj.19-686
doi:

Substances chimiques

Biomarkers 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
LDL-Receptor Related Proteins 0
Membrane Transport Proteins 0
SORL1 protein, human 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

470-475

Auteurs

Satoru Suwa (S)

Department of Cardiology, Juntendo University Shizuoka Hospital.

Manabu Ogita (M)

Department of Cardiology, Juntendo University Shizuoka Hospital.

Norihito Takahashi (N)

Department of Cardiology, Juntendo University Shizuoka Hospital.

Hideki Wada (H)

Department of Cardiology, Juntendo University Shizuoka Hospital.

Tomotaka Dohi (T)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Takatoshi Kasai (T)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Shinya Okazaki (S)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Kazunori Shimada (K)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Katsumi Miyauchi (K)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Hideaki Bujo (H)

Department of Clinical Laboratory and Experimental Research Medicine, Toho University Sakura Medical Center.

Hiroyuki Daida (H)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

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Classifications MeSH