脑源性神经营养因子(BDNF)基因Snps G196A和C270T与阿尔茨海默病的关联:一项荟萃分析

Shovit Ranjan, K. Sharma
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引用次数: 4

摘要

与AD脑组织相关的关键病理变化是细胞内神经原纤维缠结(nft)的积累和异常聚集的“反应性”蛋白,如β淀粉样蛋白(Aβ)斑块和tau[3]。老年斑、神经原纤维缠结(nft)、异常聚集的“反应性”蛋白(如β淀粉样蛋白(Aβ)和tau)、脑部炎症和接触铝等因素已经显示出AD的发展[4]。脑源性神经营养因子(Brain derived neurotrophic factor, BDNF)基因被认为是AD的重要基因之一,在AD的进展中起着重要作用[5,6]。然而,作为一种复杂的疾病,上述AD的神经病理病因不仅与基因本身有关,还可能与基因与环境因素的综合相互作用有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Brain-Derived Neurotrophic Factor (BDNF) Gene Snps G196A and C270T with Alzheimer’s Disease: A Meta-Analysis
The key pathological changes associated with AD brain tissue are the accumulation of intracellular neurofibrillary tangles (NFTs) and abnormally aggregated ‘reactive’ proteins like β amyloid (Aβ) plaques and tau [3]. Several elements, such as senile plaques, neurofibrillary tangles (NFTs), abnormally aggregated ‘reactive’ proteins like β amyloid (Aβ) and tau, brain inflammation and exposure to aluminum has already shown the development of AD [4]. Brain derived neurotrophic factor (BDNF) gene is supposed to be one of the important genes, playing a significant role in AD progression [5,6]. However, as a complex disorder, the neuropathological etiology of AD mentioned above are not due to the gene itself, but are also supposed to be associated with the combined interaction between genes and environmental factors.
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