3.8 Article

Association of neurogranin gene expression with Alzheimer's disease pathology in the perirhinal cortex

出版社

WILEY
DOI: 10.1002/trc2.12162

关键词

Alzheimer's disease; amyloid; integrative gene network; neurogranin; perirhinal cortex; synapse; tau

资金

  1. Swedish Research [860197]
  2. UK Dementia Research Institute at UCL
  3. Swedish Research Council [2017-00915]
  4. Alzheimer Drug Discovery Foundation (ADDF), USA [RDAPB-201809-2016615]
  5. Swedish Alzheimer Foundation [AF-742881]
  6. Hjarnfonden, Sweden [FO2017-0243]
  7. European Union Joint Program for Neurodegenerative Disorders [JPND2019-466-236]
  8. NIH/NIA [U01AG046170]
  9. Swedish government [ALFGBG-715986]
  10. Swedish County Councils [ALFGBG-715986]
  11. [RF1AG054014]
  12. [RF1AG057440]
  13. [R01AG057907]
  14. [U01AG052411]
  15. [R01AG068030]

向作者/读者索取更多资源

The study reveals that NRGN expression is correlated with synaptic damage in AD and associated with dementia rating and pathological diagnosis.
Introduction Synaptic damage is a key pathology of Alzheimer's disease (AD). The mechanism underlying synaptic vulnerability in AD remains elusive. Methods Using a large-scale transcriptomic dataset, we analyzed the neurogranin-centered integrative gene network and assessed the correlation of neurogranin (NRGN) gene expression with AD pathology in post mortem brains. We studied the association of NRGN expression with Clinical Dementia Rating (CDR) and neuropathological diagnosis of AD. Results We find that the genes positively correlated with NRGN expression in AD are involved in synaptic transmission and cation channel pathways. NRGN expression is correlated with amyloid and tau pathology in the perirhinal cortex of post mortem brains. NRGN expression is associated with the diagnosis of AD and correlated with CDR. Discussion Transcriptional regulation of the gene encoding for synaptic protein is involved in selective synaptic damage in AD. Identifying the genes associated with synaptic damage pathways in AD may provide targets for intervention.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据