Usefulness of Lipoprotein (a) for Predicting Outcomes After Percutaneous Coronary Intervention for Stable Angina Pectoris in Patients on Hemodialysis.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 12 2020
Historique:
received: 10 06 2020
revised: 24 08 2020
accepted: 28 08 2020
pubmed: 18 9 2020
medline: 1 1 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

Serum lipoprotein (a) level is genetically determined and remains consistent during a person's life. Previous studies have reported that people with high lipoprotein (a) level are at a high risk of cardiac events. We investigated the association between lipoprotein (a) levels and clinical outcomes after percutaneous coronary intervention (PCI) for stable angina pectoris (SAP) in hemodialysis (HD) patients. Serum lipoprotein (a) levels were measured on admission in 410 consecutive HD patients who underwent successful PCI for SAP. Patients were divided into 2 groups: low and high group having lipoprotein (a) level <40 mg/dL (n = 297) and ≧40 mg/dL (n = 113) respectively. After PCI, the incidence of major adverse cardiac event (MACE) including cardiac death, nonfatal myocardial infarction, necessity of a new coronary revascularization procedure (coronary bypass surgery, repeat target lesion PCI, PCI for a new non-target lesion) was analyzed. At a median follow-up of 24 months (12 to 37 months), MACE occurred in 188 patients (45.6%). The rate of MACE rate was significantly higher in the high lipoprotein (a) group than in the low lipoprotein (a) group (59.2% vs 40.7%, long-rank test chi-square = 12.3; p < 0.001). Cox analysis showed that high lipoprotein (a) level (Hazard Ratio, 1.62; 95% Confidence Interval, 1.19 to 2.20; p = 0.002) was an independent predictor for MACE after PCI. In conclusion, high lipoprotein (a) level was associated with a higher incidence of MACE after PCI for SAP in HD patients.

Identifiants

pubmed: 32941820
pii: S0002-9149(20)30949-8
doi: 10.1016/j.amjcard.2020.08.049
pii:
doi:

Substances chimiques

Lipoprotein(a) 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

32-37

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Keiichi Hishikari (K)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan; Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan. Electronic address: hishikari_86@yahoo.co.jp.

Hiroyuki Hikita (H)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Hiroshi Yoshikawa (H)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Fumiyuki Abe (F)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Shihoko Tsujihata (S)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Naruhiko Ito (N)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Yoshinori Kanno (Y)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Munehiro IIya (M)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Tadashi Murai (T)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Atsushi Takahashi (A)

Cardiovascular Center, Yokosuka Kyosai Hospital, Yokosuka, Japan.

Taishi Yonetsu (T)

Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

Tetsuo Sasano (T)

Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

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