No evidence for oxidative stress as a mechanism of action of hyperhomocysteinemia in humans.

Free Radic Res

Departamento de Biología, Area de Fisiologia, Facultad de Medicina, Universidad de Oviedo, Julián Clavería s/n, 33006, Oviedo, Spain.

Published: November 2004

AI Article Synopsis

  • Oxidative stress is thought to link elevated plasma homocysteine levels (p-tHcy) with cardiovascular disease (CVD), but this study found no evidence supporting that claim in elderly individuals.
  • The researchers measured various antioxidants and markers of lipid peroxidation in 123 healthy elderly subjects, but found no significant differences between those with high and low p-tHcy levels.
  • Results indicate that hyperhomocysteinemia did not increase lipid peroxidation or lead to an adaptive response in antioxidant systems, highlighting the need for further research to explore the relationship between homocysteine and atherosclerosis.

Article Abstract

Oxidative stress has been suggested as one of the physiopathologic conditions underlying the association of total plasma homocysteine (p-tHcy) with cardiovascular disease (CVD), but this hypothesis has not been validated in human epidemiological studies. We measured plasma and erythrocyte antioxidant enzymes glutathione peroxidase (GPx) and superoxide dismutase (SOD), along with serum lipid-soluble antioxidants alpha-tocopherol, beta-carotene, lycopene and retinol, in a sample of 123 healthy elderly subjects (54 men, 69 women). Plasma malondialdehyde (p-MDA) was determined as a marker of lipid peroxidation, and p-tHcy was quantified by HPLC. No significant differences were found for p-MDA, GPx or SOD activities or serum antioxidant concentrations, in subjects with elevated p-tHcy (> or =15 micromol/l) as compared to those with lower plasma homocysteine. Hyperhomocysteinemia did not lead to increased risk of having the highest p-MDA values, in either sex. We found no evidence that p-tHcy was associated with lipid peroxidation in this elderly human sample. Our results do not support the view that hyperhomocysteinemia would induce an adaptive response of antioxidant systems, either. More epidemiologic and clinical research is needed to clarify whether homocysteine promotes atherosclerosis by means of an oxidative stress mechanism.

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http://dx.doi.org/10.1080/10715760400017269DOI Listing

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