F. Rassoul et al., Plasma homocysteine and lipoprotein profile in patients with peripheral arterial occlusive disease, ANGIOLOGY, 51(3), 2000, pp. 189-196
Several studies have identified moderate hyperhomocysteinemia (HCy) as an i
ndependent risk factor for atherosclerosis. The purpose of this case contro
l study was to determine lipoprotein profile and homocysteine concentration
in serum of 85 male patients with peripheral arterial occlusive disease (P
AOD) and in 51 normolipidemic age-matched male controls. Cholesterol, trigl
ycerides, and high-density lipoprotein (HDL) cholesterol as well as subfrac
tions HDL2 and HDL3 cholesterol, low-density lipoprotein (LDL) cholesterol,
apo B, apo A-I, and lipoprotein particles LpA-I and LpA-I:A-II were measur
ed in serum. Homocysteine, folic acid, and vitamins Bg and Bit were determi
ned with the help of high-pressure liquid chromatography. The 677 C --> T m
utation in the methylenetetrahydrofolate reductase (MTHFR) gene was analyze
d in PAOD patients. Patients with peripheral arterial occlusive disease sho
wed a significantly higher mean concentration of homocysteine than control
subjects (p<0.001). There was a negative correlation between the levels of
homocysteine and vitamin B-12 as well as folic acid (for vitamin B-12: r=-0
.40 and for folic acid: r=-0.38). The prevalence of hyperhomocysteinemia (H
cy >16 mu mol/L) in the patients was 45% in contrast to 8% in controls. HDL
cholesterol, HDL3 cholesterol, Apo A-I, and Lp A-I were significantly redu
ced in patients and triglycerides were elevated. The elevated plasma homocy
steine concentration is frequently seen in homozygous carriers of a point m
utation (677 C --> T) in the methylenetetrahydrofolate reductase gene, as t
he product of this gene is an enzyme, participating in homocysteine remethy
lation. The homozygous state for the 677 C --> T mutation was found in 13.3
% of PAOD patients.