Association between enzymatic and non-enzymatic antioxidant defense mechanism with apolipoprotein E genotypes in Alzheimer disease

• Published in: Clinical biochemistry Vol. 41; no. 12; pp. 932 - 936
• Main Authors: Kharrazi, Hadi, Vaisi-Raygani, Asad, Rahimi, Zohreh, Tavilani, Haidar, Aminian, Mahdi, Pourmotabbed, Tayebeh
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.08.2008
• Subjects: Age Factors; Aged; Aged, 80 and over; Alzheimer Disease - enzymology; Alzheimer Disease - epidemiology; Alzheimer Disease - genetics; Alzheimer's disease; Antioxidants; Antioxidants - metabolism; APOE genotype; Apolipoprotein E4 - genetics; Case-Control Studies; Catalase; Catalase - blood; DNA - genetics; Erythrocytes - enzymology; Female; Genetic Variation; Genotype; Glutathione peroxidase; Glutathione Peroxidase - blood; Humans; Iran - epidemiology; Male; Oxidative Stress; Polymerase Chain Reaction; Risk Factors; Superoxide dismutase; Superoxide Dismutase - blood; Total antioxidant status; Iran; Antioxidants; Glutathione peroxidase; Oxidative stress; Catalase; Superoxide dismutase; Alzheimer's disease; Total antioxidant status; APOE genotype
• ISSN: 0009-9120; 1873-2933
• DOI: 10.1016/j.clinbiochem.2008.05.001

There are evidence suggesting that APOE-ɛ4 allele play an important role in the pathogenesis of Alzheimer's disease (AD) by reducing peripheral levels and activities of a broad spectrum of nonenzymatic and enzymatic antioxidants systems. However, the link between APOE genotype, oxidative stress, and AD has yet to be established. In this study we examined whether antioxidant defense mechanism exacerbates the risk of AD in individual carrying APOE-ɛ4 allele in a population from Tehran, Iran. We determined the enzymatic activities of the erythrocyte Cu–Zn superoxide dismutase (Cu–Zn SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and serum level of total antioxidant status(TAS) in various APOE genotypes in 91 patients with AD and 91 healthy subjects as control group (age and sex-matched). The results showed that the TAS level and the activities of enzymatic antioxidants CAT and GSH-Px were significantly lower and the SOD activity was significantly higher in AD patients compared to controls. The AD patients with APOE-ɛ4 allele genotype had significantly lower serum TAS concentration and lower erythrocytes GSH-Px and CAT activities ( p = 0.001) but significantly higher erythrocytes Cu–Zn SOD activity ( p = 0.001) than the non-APOE-ɛ4 carrier AD and the control group. In addition, the association observed between the factors involved in an antioxidant defense mechanism and APOE-ɛ4 allele in AD increased with age of the subjects. These data indicate that the reduced serum level of TAS and activity of CAT, GSH-Px and increased SOD exacerbate the risk of AD in individuals carrying APOE-ɛ4 allele. The reduced antioxidants defense in APOE–ɛ4 allele carrier may contribute to beta-amyloidosis. This effect, however, is more pronounced in the AD patients older than 75 years of age. This suggests that a therapeutic modality should be considered for these subjects.