کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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331106 | 1433634 | 2009 | 6 صفحه PDF | دانلود رایگان |

Oxidative stress is a relevant pathomechanism in Alzheimer's disease (AD) and gene variations in the glutathione S-transferase M3 gene (GSTM3), involved in the detoxification of oxygen radicals, might influence the risk of AD.We investigated the effect of three polymorphisms in GSTM3: rs1332018 (C/A); rs1799735 (del/AGG); rs7483 (G/A), on the risk of AD in 363 AD patients and 358 healthy controls.Single marker association analyses revealed that the AGG/AGG genotype of the GSTM3 rs1799735 (del/AGG) polymorphism was associated with an increased risk of AD (p = 0.05), especially in the group of APOE4-allele non-carriers (p = 0.004; OR = 2.07). Examination of the haplotypes identified a two-marker haplotype (C/AGG) consisting of rs1332018 (C/A) and rs1799735 (del/AGG) to increase the risk of AD (p = 0.029), this effect was also most prevalent in APOE4-allele non-carriers (p = 0.009; OR = 1.95). The population attributable risk of this haplotype in APOE4-allele non-carriers was 32.2%.Our results suggest that there is a group of AD patients in which variations in metabolism of oxidative stress play an important role.
Journal: Neurobiology of Aging - Volume 30, Issue 5, May 2009, Pages 691–696