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