Ic. Klausen et al., APO(A) PHENOTYPES AND LP(A) CONCENTRATIONS IN OFFSPRING OF MEN WITH AND WITHOUT MYOCARDIAL-INFARCTION - THE EARS STUDY, Arteriosclerosis, thrombosis, and vascular biology, 15(8), 1995, pp. 1001-1008
In the European Atherosclerosis Research Study, genetic and environmen
tal markers of risk of premature coronary heart disease were compared
in offspring of men with and without myocardial infarction before the
age of 55 years. Cases were 682 students with a paternal history of my
ocardial infarction, and control subjects were 1312 students without s
uch a history. The students were enrolled in 14 universities in five E
uropean regions (Finland, Great Britain, and northern, middle, and sou
thern Europe). Lipoprotein(a) [Lp(a)] concentrations were skewed towar
ds lower concentrations in both cases (median, 7.3 mg/dL; 95% confiden
ce interval, 6.3 to 8.1 mg/dL) and control subjects (median, 6.6 mg/dL
; 95% confidence interval, 6.1 to 7.2 mg/dL) (P = .37). Significantly
more northern European male cases than control subjects had Lp(a) leve
ls exceeding 30 mg/dL (P = .040), but this did not pertain to females
(P = .29), and overall, there was no difference between cases (16.5%)
and control subjects (15.5%) in the frequency of Lp(a) concentrations
above 30 mg/dL (P = .63). As expected, there was a significant (P < .0
1) inverse relationship between apo(a) molecular size and Lp(a) concen
tration. In Great Britain there was a significant difference in phenot
ype distribution between cases and control subjects (P = .035), due ma
inly to a high frequency of the apo(a) S2 isoform in cases. A similar
but statistically insignificant tendency was seen in northern European
s. In the three other regions, however, the distribution of apo(a) phe
notypes among cases and controls was similar: and in the study populat
ion overall, the distribution of apo(a) phenotypes did not differ sign
ificantly (P = .74) between cases and control subjects.