Shvetcov Artur, Johnson Erik C B, Winchester Laura M, Walker Keenan A, Wilkins Heather M, Thompson Terri G, Rothstein Jeffrey D, Krish Varsha, Imam Farhad B, Burns Jeffrey M, Swerdlow Russell H, Slawson Chad, Finney Caitlin A
Neurodegeneration and Disease Modelling Research Group, Westmead Institute for Medical Research, The University of Sydney, Westmead, New South Wales, Australia.
School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
Nat Med. 2025 Jul 15. doi: 10.1038/s41591-025-03835-z.
The APOE ε4 genetic variant is the strongest genetic risk factor for late-onset Alzheimer's disease (AD) and is increasingly being implicated in other neurodegenerative diseases. Using the Global Neurodegeneration Proteomics Consortium SomaScan dataset covering 1,346 cerebrospinal fluid (CSF) and 9,924 plasma samples, we used machine learning-based proteome profiling to identify an APOE ε4 proteomic signature shared across individuals with AD, frontotemporal dementia (FTD), Parkinson's disease dementia (PDD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS) and nonimpaired controls. This signature was enriched in pro-inflammatory immune and infection pathways as well as immune cells, including monocytes, T cells and natural killer cells. Analysis of the dorsolateral prefrontal cortex proteome for 262 donors from the Accelerating Medicines Partnership for AD UPenn Proteomics Study revealed a consistent APOE ε4 phenotype, independent of neurodegenerative pathology, including amyloid-β tau and gliosis for all diseases, as well as TDP-43 in ALS and FTD cases, and α-synuclein in PD and PDD cases. While systemic proteomic changes were consistent across APOE ε4 carriers, their relationship with clinical and lifestyle factors, such as hypertension and smoking, varied by disease. These findings suggest APOE ε4 confers a systemic biological vulnerability that is necessary but not sufficient for neurodegeneration, emphasizing the need to consider gene-environment interactions. Overall, our study reveals a conserved APOE ε4-associated pro-inflammatory immune signature persistent across the brain, CSF and plasma irrespective of neurodegenerative disease, highlighting a fundamental, disease-independent biological vulnerability to neurodegeneration. This work reframes APOE ε4 as a pleiotropic immune modulator rather than an AD-specific risk gene, providing a foundation for precision biomarker development and early intervention strategies across neurodegenerative diseases.
APOE ε4基因变异是晚发型阿尔茨海默病(AD)最强的遗传风险因素,并且越来越多地与其他神经退行性疾病相关。利用全球神经退行性疾病蛋白质组学联盟的SomaScan数据集,该数据集涵盖1346份脑脊液(CSF)样本和9924份血浆样本,我们使用基于机器学习的蛋白质组分析来识别在患有AD、额颞叶痴呆(FTD)、帕金森病痴呆(PDD)、帕金森病(PD)、肌萎缩侧索硬化症(ALS)的个体以及未受损对照中共享的APOE ε4蛋白质组特征。该特征在促炎免疫和感染途径以及免疫细胞中富集,包括单核细胞、T细胞和自然杀伤细胞。对来自加速药物合作组织AD宾夕法尼亚大学蛋白质组学研究的262名捐赠者的背外侧前额叶皮质蛋白质组分析显示,存在一致的APOE ε4表型,与神经退行性病理无关,包括所有疾病的淀粉样β蛋白、tau蛋白和胶质增生,以及ALS和FTD病例中的TDP - 43,以及PD和PDD病例中的α - 突触核蛋白。虽然APOE ε4携带者的全身蛋白质组变化是一致的,但它们与临床和生活方式因素(如高血压和吸烟)的关系因疾病而异。这些发现表明APOE ε4赋予了一种全身生物学易损性,这是神经退行性变所必需但不充分的,强调了考虑基因 - 环境相互作用的必要性。总体而言,我们的研究揭示了一种保守的、与APOE ε4相关的促炎免疫特征,无论神经退行性疾病如何,在大脑、CSF和血浆中持续存在,突出了对神经退行性变的一种基本的、与疾病无关的生物学易损性。这项工作将APOE ε4重新定义为一种多效性免疫调节剂,而不是一个特定于AD的风险基因,为跨神经退行性疾病的精准生物标志物开发和早期干预策略奠定了基础。