伊朗阿尔茨海默病患者B2-AR、TLR2、PICALM和BDNF基因变异及其对利匹的明反应的研究

Parvin Mohabattalab, F. R. Rad, H. Zamani, Fariba Shirvani, M. Zamani
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摘要

阿尔茨海默病(AD)是一种毁灭性的神经退行性疾病,具有多基因和多因子遗传,由记忆力和其他认知功能的逐渐丧失决定。阿尔茨海默病的特征是细胞外淀粉样蛋白聚集(Aβ)、神经元内神经原纤维缠结等标志性病理改变,导致脑萎缩和神经组织丧失[1,2]。阿尔茨海默病根据发病年龄分为早发性AD (EOAD)和晚发性AD (LOAD)[3]。而且,根据家族史,它被分类为散发性(SAD)或家族性阿尔茨海默病(FAD)[4]。阿尔茨海默病的发病机制涉及多种遗传和环境因素,使得该病的病因复杂,检测方法摘要
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of B2-AR, TLR2, PICALM, and BDNF Gene Variants in Iranian Alzheimer’s Patients and Their Response to Rivastigmine
Alzheimer’s disease (AD) is a devastating neurodegenerative disorder with polygenic and multifactorial inheritance, determined by progressive loss of memory and other cognitive functions. AD is characterized by hallmark pathological changes such as extracellular aggregation of amyloid β (Aβ), intraneuronal neurofibrillary tangles that lead to brain atrophy and loss of neural tissue [1,2]. Alzheimer’s disease is categorized according to the age of onset as early-onset (EOAD) or lateonset AD (LOAD) [3]. And, based on family history, it is classified as sporadic (SAD) or familial Alzheimer’s disease (FAD) [4]. There are various genetic and environmental factors involved in the pathogenesis of AD which makes the etiology of the disease complicated however, testing for Abstract
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