ApoE: The Non-Protagonist Actor in Neurological Diseases.

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY Genes Pub Date : 2024-10-30 DOI:10.3390/genes15111397
Lorenzo Grimaldi, Eleonora Bovi, Rita Formisano, Giulia Sancesario
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Abstract

Background: Apolipoprotein E (APOE = gene, ApoE = protein) is a glycoprotein involved in the biological process of lipid transportation and metabolism, contributing to lipid homeostasis. APOE has been extensively studied for its correlation with neurodegenerative diseases, in particular Alzheimer's disease (AD), where the possession of the epsilon 4 (E4) allele is established as a risk factor for developing AD in non-familiar sporadic forms. Recently, evidence suggests a broad involvement of E4 also in other neurological conditions, where it has been shown to be a predictive marker for worse clinical outcomes in Parkinson's disease (PD), brain trauma, and disturbances of consciousness. The mechanisms underlying these associations are complex and involve amyloid-β (Aβ) peptide accumulation and neuroinflammation, although many others have yet to be identified.

Objectives: The aim of this review is to overview the current knowledge on ApoE as a non-protagonist actor in processes underlying neurodegenerative diseases and its clinical significance in AD, PD, acquired brain trauma, and Disorders of Consciousness (DoC). Ethical implications of genetic testing for APOE variants and information disclosure will also be briefly discussed.

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载脂蛋白E:神经系统疾病中的非主角。
背景:载脂蛋白 E(APOE = 基因,ApoE = 蛋白质)是一种糖蛋白,参与脂质运输和代谢的生物过程,促进脂质平衡。APOE 与神经退行性疾病,尤其是阿尔茨海默病(AD)的相关性已被广泛研究,其中epsilon 4(E4)等位基因已被确定为非熟悉散发性阿尔茨海默病的危险因素。最近,有证据表明 E4 也广泛涉及其他神经系统疾病,在帕金森病(PD)、脑外伤和意识障碍等疾病中,E4 已被证明是临床结果较差的预测标志。这些关联的机制很复杂,涉及淀粉样蛋白-β(Aβ)肽的积累和神经炎症,但还有许多其他机制尚未确定:本综述旨在概述当前关于载脂蛋白E在神经退行性疾病基础过程中的非拮抗剂作用及其在AD、PD、获得性脑损伤和意识障碍(DoC)中的临床意义的知识。此外,还将简要讨论 APOE 变异基因检测和信息披露的伦理意义。
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来源期刊
Genes
Genes GENETICS & HEREDITY-
CiteScore
5.20
自引率
5.70%
发文量
1975
审稿时长
22.94 days
期刊介绍: Genes (ISSN 2073-4425) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to genes, genetics and genomics. It publishes reviews, research articles, communications and technical notes. There is no restriction on the length of the papers and we encourage scientists to publish their results in as much detail as possible.
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