Transcriptomic analysis of lipid metabolism genes in Alzheimer’s disease: highlighting pathological outcomes and compartmentalized immune status

Author:

Sun Yue1,Jiang Mengni2,Long Xiang2,Miao Yongzhen2,Du Huanhuan2,Zhang Ting2,Ma Xuejun3,Zhang Yue1,Meng Hongrui2

Affiliation:

1. Department of Neurology, Shanghai East Hospital of Tongji University School of Medicine

2. Institute of Neuroscience, Soochow University

3. School of Mathematical Sciences, Soochow University

Abstract

Abstract

The dysregulation of lipid metabolism has been strongly associated with Alzheimer's Disease (AD); however, the biomedical implications and clinical relevance of these findings have not been systematically examined. Here, we conducted a comprehensive bioinformatic evaluation of AD-derived transcriptome datasets from postnatal brains and peripheral blood. We utilized differential gene expression and hierarchical clustering to identify co-expressed modules of lipid metabolism genes in patients based on their molecular functions in biological enrichment and molecular pathway analysis, association with pathological phenotypes, and molecular network correlation. Additionally, we analyzed the expression patterns of these genes in immune and nonimmune cells as well as cell type enrichments in both brain tissue and peripheral blood. By categorizing patients into distinct transcriptional clusters and stratified groups, we found enrichment in biological pathways for neurodegenerative diseases, oxidative phosphorylation, synaptic transmission, unexpected infections, and molecular functions for cellular translation and energy production in the stratified clusters and groups. Biological network analysis indicates striking differences between lipid-metabolism differential expression genes (DEGs) in the periphery and CNS, with restricted processes being enriched. Notably, neurons, glial cells involved in neuroinflammation, and peripheral blood immune cell infiltration revealed a marked disparity in the clustering subgroups in patients’ hippocampi and peripheral regions. Differentially expressed genes such as PLD3, NDUFAB1, OXCT1, PI4KA, and AACS in the brain and DBI, MBOAT7, and RXRA in the periphery correlate well with disease pathologies and immune cell preferences. These results suggest that lipid metabolism is critical for disease progression and immune cell activation, thus providing an innovative approach to diagnosing and treating AD.

Publisher

Springer Science and Business Media LLC

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3