LOW-DENSITY-LIPOPROTEIN PARTICLE-SIZE IS NOT A DISCRIMINATING MARKER FOR ATHEROGENIC RISK IN MALE OFFSPRING OF PARENTS WITH EARLY CORONARY-ARTERY DISEASE
Ah. Slyper et al., LOW-DENSITY-LIPOPROTEIN PARTICLE-SIZE IS NOT A DISCRIMINATING MARKER FOR ATHEROGENIC RISK IN MALE OFFSPRING OF PARENTS WITH EARLY CORONARY-ARTERY DISEASE, Metabolism, clinical and experimental, 46(8), 1997, pp. 954-958
The aim of this study was to assess the importance of low-density lipo
protein (LDL) particle size as a marker of atherogenic risk in male of
fspring of a parent with early coronary artery disease (CAD) before th
e age of 60 years. CAD-positive (CAD(+)) offspring were recruited into
two groups based on age, 15 to 30 years (n = 20) and 31 to 45 years (
n = 41), and matched to CAD-negative (CAD(-)) offspring by age and bod
y mass index (BMI) (n = 20 and 21 per group). LDL peak particle diamet
er was assessed by polyacrylamide gradient gel electrophoresis. There
was no significant difference in LDL peak particle diameter between CA
D(+) and CAD(-) offspring (26.2 +/- 0.1 v 26.2 +/- 0.1 nm, mean +/- SE
). There was also no difference between CAD(+) offspring and CAD(-) of
fspring when comparisons were made within their own age group (26.5 +/
- 0.1 nm in younger CAD(+) offspring v 26.2 +/- 0.1 nm in younger CAD(
-) offspring, and 26.0 +/- 0.1 nm in older CAD(+) offspring v 26.1 +/-
0.2 nm in older CAD(-) offspring). Peak particle diameter was signifi
cantly greater in younger CAD(+) offspring than in older CAD(+) offspr
ing (26.5 + 0.1 v 26.0 +/- 0.1 nm, P < .05). We conclude that small LD
L particle size is not a discriminating marker for early atherogenic r
isk, and that measurement of LDL particle size has limited value in th
e assessment of coronary risk, at least in the age ranges we studied.
Copyright (C) 1997 by W.B. Saunders Company.