کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6280157 1615085 2016 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Association study of the BIN1 and IL-6 genes on Alzheimer's disease
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Association study of the BIN1 and IL-6 genes on Alzheimer's disease
چکیده انگلیسی


- BIN1 (rs744373) and IL-6 (rs1800795) SNPs were studied in Alzheimer's disease (AD).
- No association with AD for both SNPs in a located southeast Brazilian population.
- The results suggest that they were not implicated with AD for all populations.

Genome-wide association study (GWAS) has identified several novel genes associated with the risk of Alzheimer's disease (AD), which is a progressive neurodegenerative disease in elders. However, most of the novel genes have not been validated through replication in separated populations. Among them, the BIN1 gene is involved in endocytosis and intracellular trafficking as well as in the formation of β amyloid plaques and neurofibrillary tangles, which are the main pathological hallmarks of AD. The IL-6 gene has also been frequently associated with AD; however, consistent results have not been found. IL-6, a cytokine from the immune system, is implicated in the pathogenesis of several degenerative diseases. Similar to BIN1, it is suggested that IL-6 is also involved in the formation of β amyloid plaques. In this case-control study, we aimed to investigate whether single nucleotide polymorphisms in the BIN1 (rs744373) and IL-6 (rs1800795) genes are associated with AD. Genotype frequencies were evaluated via PCR-RFLP in 82 late-onset AD patients and 159 elderly healthy controls, who were matched by age and gender. In this study, no association was found for either polymorphism, suggesting that these genes are not implicated in the aetiology of AD in all populations.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience Letters - Volume 614, 12 February 2016, Pages 65-69
نویسندگان
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