Plasma homocysteine and lipoprotein profile in patients with peripheral arterial occlusive disease

Citation
F. Rassoul et al., Plasma homocysteine and lipoprotein profile in patients with peripheral arterial occlusive disease, ANGIOLOGY, 51(3), 2000, pp. 189-196
Citations number
28
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
ANGIOLOGY
ISSN journal
00033197 → ACNP
Volume
51
Issue
3
Year of publication
2000
Pages
189 - 196
Database
ISI
SICI code
0003-3197(200003)51:3<189:PHALPI>2.0.ZU;2-G
Abstract
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.