Lipoprotein (a) and its position among other risk factors of atherosclerosis
Lipoprotein(a) [Lp(a)] comprises of an LDL particle and apolipoprotein(a) [apo(a)] and its elevated levels are considered a risk factor for atherosclerosis. The aim of our study was to find out whether elevated Lp(a) levels are associated with increased risk of atherosclerosis in patients with multi...
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Published in | Physiological research Vol. 57; no. 5; pp. 777 - 784 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Czech Republic
Institute of Physiology
01.01.2008
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Subjects | |
Online Access | Get full text |
ISSN | 0862-8408 1802-9973 |
DOI | 10.33549/physiolres.931133 |
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Summary: | Lipoprotein(a) [Lp(a)] comprises of an LDL particle and
apolipoprotein(a) [apo(a)] and its elevated levels are considered
a risk factor for atherosclerosis. The aim of our study was to find
out whether elevated Lp(a) levels are associated with increased
risk of atherosclerosis in patients with multiple other risk factors.
We further tested the association of three polymorphisms of the
apo(a) gene promoter with Lp(a) levels. No significant correlation
was detected between Lp(a) levels and lipid and clinical
parameters tested. The study demonstrated a significantly
(p=0.0219) elevated Lp(a) level (mean 28±35 mg/dl, median
0.14) in patients with coronary heart disease (CHD). In a group
with premature CHD the correlation was not significant anymore.
There was a significant correlation between polymorphic loci of
the promoter region of apo(a) gene and Lp(a) levels (+93C>T,
p=0.0166, STR, p<0.0001). Our study suggests that elevated
Lp(a) level is an independent risk factor of CHD in carriers of
other important CHD risk factors. Observed association of
sequence variants of the promoter of apo(a) gene with Lp(a)
levels is caused in part due to linkage to a restricted range of
apo(a) gene length isoforms. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0862-8408 1802-9973 |
DOI: | 10.33549/physiolres.931133 |