J. Constans et al., LIPOPROTEIN(A) IN 505 HOSPITALIZED-PATIENTS WITH VARIOUS PATHOLOGICALSTATES - CORRELATIONS WITH CARDIOVASCULAR-DISEASES AND THERAPIES, International angiology, 15(1), 1996, pp. 1-5
Objective. Our aim was to study the lipoprotein (a) (Lp(a)) levels in
various pathological states. Experimental design. This investigation w
as prospective and included a healthy control group. Setting. This stu
dy was carried out in two internal medicine and angiology services in
teaching hospitals. Patients. 505 patients were included with various
diseases: 66 acute infections, 9 HIV infections, 25 cancers, 86 diabet
es, 36 systemic diseases, 94 atheromatous vascular disease, 27 arteria
l hypertensions. A control group was composed of 21 healthy subjects.
Interventions. There was no therapeutic intervention but cardiovascula
r treatments were recorded. Measures. Serum Lp(a), total cholesterol,
triglycerides, HDL-cholesterol, calculated LDL-cholesterol, apolipopro
teins A-I and B were measured together with inflammatory parameters, s
erum creatinine, proteinuria, serum aminotransferase activity. Results
. There was no difference in Lp(a) levels between controls and each pa
tient group. However, a correlation was found in systemic diseases bet
ween Lp(a) and C reactive protein (r=0.371, p=0.026) or serum albumin
concentration (r=-0.453, p=0.006). In hypertension, Lp(a) correlated w
ith serum creatinine (r=0.420, p=0.03). In the whole patient populatio
n, Lp(a) was correlated with cholesterol (r=0.156, p=0.0001), apolipop
rotein B (r= 0.215, p=0.0001), age (r=0.108, p=0.015), arterial events
(r=0.174, p=0.0001) and platelet anti-aggregant drugs (r=0.169, p=0.0
001). Conclusions. Lp(a), was related to atheromatous events and in sy
stemic diseases to inflammation, suggesting that Lp(a) might vary in s
ome patients in a manner similar to acute phase proteins.