Objectives: The aim of this work is to study the effect of different b
iological factors that could affect Lp(a) level in a presumably health
y population and to establish reference limits. Methods: We selected 7
23 subjects (367 men and 356 women) for the age interval 4 to 64 years
for evaluation. Results: The distribution of Lp(a) is not Gaussian; 5
0.5% of subjects had Lp(a) concentrations under 0.10 g/l and the value
for the 75th percentile was 0.27 g/l and 0.57 g/l for the 90th percen
tile. No relationship was observed between Lp(a) concentration and cho
lesterolaemia, triglyceridaemia, glycaemia, inflammatory proteins (oro
somucoide and CRP), overweight, tobacco consumption and oral contracep
tive use. The menopause state in women was a factor correlated with in
creased Lp(a) but this increase was not significant. Moreover, alcohol
consumption (more than 44 g per day in men and more than 22 g per day
in women) was associated with lower Lp(a) values. Among familial card
iovascular risks, only paternal listing of hypertension was associated
with Lp(a) concentration in men. Conclusion: The measurement of Lp(a)
in a young subject could be used as a genetic marker of cardiovascula
r risk associated with abnormal lipid metabolism and thrombosis phenom
ena.