4.6 Article

Detecting Diagnostic Biomarkers of Alzheimer's Disease by Integrating Gene Expression Data in Six Brain Regions

期刊

FRONTIERS IN GENETICS
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2019.00157

关键词

Alzheimer's disease; biomarker discovery; gene expression; data integration; classification; machine learning

资金

  1. National Nature Science Foundation of China (NSFC) [61572287, 61533011]
  2. Innovation Method Fund of China (Ministry of Science and Technology of China) [2018IM020200]
  3. Shandong Provincial Key Research and Development Program [2018GSF118043]
  4. Department of Science and Technology of Shandong Province, China [2017CXGC1502, 2015ZDXX0801A01]
  5. Fundamental Research Funds of Shandong University [2016JC007]
  6. Scientific Research Foundation for the Returned Overseas Chinese Scholars, Ministry of Education of China

向作者/读者索取更多资源

Alzheimer's disease (AD) is a neurodegenerative and progressive disease, which often causes irreversible damages to the cerebrum. The pathogenesis of AD is far from being fully understood, while there are some popular hypotheses. So far, the diagnosis of AD relies only on clinical screening in the form of imaging techniques or cerebrospinal fluid analysis, which may lead to inaccurate evaluation and then cause the delay of suitable treatments. While molecular biomarkers provide promising alternatives of establishing correct relationships between genotypes and phenotypes of clinical symptoms. In this paper, we propose a machine-learning-based method of identifying potential diagnostic biomarkers of AD based on gene coexpression network by integrating gene expression profiles in six brain regions. After building an integrated gene coexpression network of multiple brain regions, we decompose the differential network into some subnetwork modules. The module candidates from these coexpressed gene communities are then identified by screening their discriminative powers in control from disease samples. The potential biomarkers are then validated by multiple cross-validations and functional enrichment analyses. If the biomarkers successfully pass clinical significance tests, they can be used as a reference for clinical diagnosis after wet-experimental validations.

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