The ''oxidation hypothesis'' states that oxidative modification of low
-density lipoprotein (LDL) is important in the pathogenesis of the ath
erosclerotic lesion. We studied 15 families (fathers, mothers and male
twins of 16 to 18 years of age) to investigate the familial aggregati
on of LDL oxidation. As an indicator of LDL oxidation products we meas
ured baseline levels of conjugated dienes extracted from LDL (LDL-BDC)
. For this analysis LDL was first isolated by rapid precipitation with
buffered heparin. LDL-BDC was highest in fathers (mean 673 Delta Abs
per mg LDL cholesterol, 95% confidence interval (CI) 547-800) followed
by mothers (500, 95% CI 408-592) and twins (383, 95% CI 337-430). The
re was a high correlation in the LDL-BDC between the identical twins (
r = 0.81, 95% CI 0.44-0.95), but no correlation between the parents (r
= -0.36). The LDL-BDC of boys correlated positively with that of fath
ers (r = 0.49, 95% CI 0.16-0.72), but not with that of mothers (r = 0.
00). Highly significant positive correlations were observed between LD
L-BDC and serum lipid risk factors among parents, but among twins the
correlations were usually weaker. Our study suggests that inherited fa
ctors contribute to interindividual variability in the oxidative modif
ication of LDL.