阿尔茨海默病的遗传表型:机制与潜在疗法
Genetic Phenotypes of Alzheimer's Disease: Mechanisms and Potential Therapy.
作者信息
Quan Meina, Cao Shuman, Wang Qi, Wang Shiyuan, Jia Jianping
机构信息
Innovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, 100053 China.
National Medical Center for Neurological Disorders and National Clinical Research Center for Geriatric Diseases, Beijing, 100053 China.
出版信息
Phenomics. 2023 Apr 3;3(4):333-349. doi: 10.1007/s43657-023-00098-x. eCollection 2023 Aug.
Years of intensive research has brought us extensive knowledge on the genetic and molecular factors involved in Alzheimer's disease (AD). In addition to the mutations in the three main causative genes of familial AD (FAD) including and genes, studies have identified several genes as the most plausible genes for the onset and progression of FAD, such as , , and . The allele is reported to be the strongest genetic risk factor for sporadic AD (SAD), and it also plays an important role in FAD. Here, we reviewed recent developments in genetic and molecular studies that contributed to the understanding of the genetic phenotypes of FAD and compared them with SAD. We further reviewed the advancements in AD gene therapy and discussed the future perspectives based on the genetic phenotypes.
多年的深入研究让我们对阿尔茨海默病(AD)涉及的遗传和分子因素有了广泛了解。除了家族性AD(FAD)的三个主要致病基因(包括[具体基因1]、[具体基因2]和[具体基因3])发生突变外,研究还确定了几个基因是FAD发病和进展最可能的相关基因,如[具体基因4]、[具体基因5]和[具体基因6]。据报道,[具体基因7]等位基因是散发性AD(SAD)最强的遗传风险因素,它在FAD中也起着重要作用。在此,我们回顾了有助于理解FAD遗传表型的遗传和分子研究的最新进展,并将它们与SAD进行比较。我们还回顾了AD基因治疗的进展,并基于遗传表型讨论了未来前景。