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
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.