G. Feussner et al., APOLIPOPROTEIN (A) PHENOTYPES AND LIPOPROTEIN (A) CONCENTRATIONS IN PATIENTS WITH TYPE-III HYPERLIPOPROTEINEMIA, Journal of internal medicine, 235(5), 1994, pp. 425-430
Objectives, The familial lipoprotein disorder type III hyperlipoprotei
naemia (HLP) carries a marked increase in the risk of accelerated and
premature atherosclerosis, but there is considerable variation amongst
affected individuals-in their susceptibility to cardiovascular diseas
e (CVD). Therefore, it was the aim of our study to investigate the pos
sible influence of lipoprotein (a) [Lp(a)] in the pathogenesis of type
m HLP. Design. Apolipoprotein (a) [apo(a)] phenotypes and Lp(a) conce
ntrations were determined in patients with the disease and in an appro
priate control group. Setting. University out-patient lipid disorder c
linic. Subjects. Seventy-six apoE-2 homozygous patients with type III
HLP and 76 normolipidaemic and healthy age- and sex-matched controls.
Main outcome measures. The frequencies of different apo(a) phenotypes
and their correlations with Lp(a) serum concentrations were determined
in patients and controls. Results. Lp(a) concentrations were not sign
ificantly different in type III HLP patients (14.1 +/- 19.1 mg dl(-1))
as compared with the controls (13.3 +/- 16.2 mg dl(-1); P = 0.549, NS
). In addition, there was no significant difference in apo(a) phenotyp
e frequencies amongst both groups (0.2 > P > 0.1). Conclusions. We con
clude that the apo(a) polymorphism does not participate (to a signific
ant extent) in the phenotypical expression of type III HLP.