Serum lipoprotein(a) concentrations and apolipoprotein(a) isoforms: association with the severity of clinical presentation in patients with coronary heart disease

Citation
Cs. Katsouras et al., Serum lipoprotein(a) concentrations and apolipoprotein(a) isoforms: association with the severity of clinical presentation in patients with coronary heart disease, J CARD RISK, 8(5), 2001, pp. 311-317
Citations number
49
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
JOURNAL OF CARDIOVASCULAR RISK
ISSN journal
13506277 → ACNP
Volume
8
Issue
5
Year of publication
2001
Pages
311 - 317
Database
ISI
SICI code
1350-6277(200110)8:5<311:SLCAAI>2.0.ZU;2-1
Abstract
Objective The aim of this study was to investigate the possible association s between lipoprotein(a) [Lp(a)] concentrations or apolipoprotein(a) isofor ms and the mode of clinical presentation of coronary heart disease (CHID) ( acute thrombotic event or not). Methods A total of 131 CHD patients and 71 age- and gender-matched individu als without known CAD (free of symptoms of heart disease) were enrolled in the study. CHD patients were classified into patients with a history of an acute coronary syndrome (ACS, n=94) and patients with stable angina (SA, n= 37). Lp(a) levels were measured with an ELISA method, whereas apolipoprotei n(a) isoform analysis was performed (in all patients and 33 controls) by el ectrophoresis in 1.5% SDS-agarose gels followed by immunoblotting. Isoform size was expressed as the number of kringle 4 (K4) repeats. Results ACS patients had higher Lp(a) plasma levels [21.9 (0.8-84.1) mg/dl] and a greater proportion of elevated (greater than or equal to 30 mg/dl) L p(a) concentrations (25.5%) compared with SA patients [9.2 (0.8-50.5) mg/dl , P < 0.01 and 10.8%, P < 0.05] and controls [8.0 (0.8-55.0) mg/dl, P < 0.0 1 and 11.2%, P < 0.05], while there were no differences between SA patients and controls. The median apolipoprotein(a)-isoform size was 26 K4. In 17 ( 10%) patients we could not detect any apolipoprotein(a) isoform bands by im munoblotting. ACS patients had a higher proportion of isoforms < 26 K4 (low molecular weight) than SA patients (56/85 vs. 12/33, P < 0.005) and contro ls (10/29, P < 0.005). Conclusions CAD patients with a history of ACS have higher Lp(a) plasma lev els and a significantly higher proportion of low molecular weight apolipopr otein(a) isoforms compared with patients with SA or to controls. (C) 2001 L ippincott Williams & Wilkins.