LIPOPROTEIN(A) AND ASYMPTOMATIC CAROTID-ARTERY DISEASE - EVIDENCE OF A PROMINENT ROLE IN THE EVOLUTION OF ADVANCED CAROTID PLAQUES - THE BRUNECK STUDY

Citation
J. Willeit et al., LIPOPROTEIN(A) AND ASYMPTOMATIC CAROTID-ARTERY DISEASE - EVIDENCE OF A PROMINENT ROLE IN THE EVOLUTION OF ADVANCED CAROTID PLAQUES - THE BRUNECK STUDY, Stroke, 26(9), 1995, pp. 1582-1587
Citations number
58
Categorie Soggetti
Neurosciences,"Cardiac & Cardiovascular System","Peripheal Vascular Diseas","Clinical Neurology
Journal title
StrokeACNP
ISSN journal
00392499
Volume
26
Issue
9
Year of publication
1995
Pages
1582 - 1587
Database
ISI
SICI code
0039-2499(1995)26:9<1582:LAACD->2.0.ZU;2-M
Abstract
Background and Purpose Elevated levels of lipoprotein(a) [Lp(a)] have been reported in association with symptomatic coronary and carotid art ery disease. Relevancy of Lp(a) as a risk predictor of presymptomatic atherosclerosis in general populations is not well established. Method s Serum Lp(a) distribution and its relation to sonographically assesse d carotid atherosclerosis were examined in a random sample of 885 men and women aged 40 to 79 years (Bruneck Study). Results Logistic regres sion analysis revealed a binary-type association between Lp(a) and car otid artery disease, with the threshold level of Lp(a) for an enhanced atherosclerosis risk defined at 32 mg/dL. The strength of relation in creased with advancing severity of carotid atherosclerosis (odds ratio s for Lp(a), 1.8 for nonstenotic and 4.7 for stenotic carotid artery d isease; P<.001). Lp(a) was unaffected by environmental factors except for a significant decrease in women taking hormone replacement therapy (P<.05). In a multivariate approach, Lp(a) turned out to be an indepe ndently significant predictor of carotid atherosclerosis (P<.001). No differential effect of Lp(a) on atherosclerosis (effect modification) was observed for sex, age, low-density lipoprotein cholesterol, apolip oprotein A-I and B, fasting glucose, diabetes, or hypertension. Howeve r, the Lp(a)-atherosclerosis relation was significantly modified by fi brinogen (P<.01) and antithrombin III (P<.05). Conclusions The present study demonstrates a strong and independent association between eleva ted Lp(a) levels and carotid atherosclerosis in a large randomized pop ulation and provides evidence of a potential role of Lp(a) in the evol ution of carotid stenosis. Apart from atherogenicity of Lp(a) choleste rol, interference with fibrinolysis of atheroma-associated clots and f ibrin deposits in the arterial wall may achieve pathophysiological sig nificance.