4.7 Article

Identification of hub proteins in cerebrospinal fluid as potential biomarkers of Alzheimer's disease by integrated bioinformatics

Journal

JOURNAL OF NEUROLOGY
Volume 270, Issue 3, Pages 1487-1500

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-022-11476-2

Keywords

Alzheimer's disease; Biomarkers; Proteomic database; Cerebrospinal fluid; Machine learning

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This study used bioinformatics methods to identify potential candidate hub proteins in cerebrospinal fluid for Alzheimer's disease diagnosis. These identified hub proteins, mainly involved in glycometabolism pathways, were upregulated in the cerebrospinal fluid of Alzheimer's disease patients compared to control individuals, and showed excellent discriminatory ability for Alzheimer's disease diagnosis. These hub proteins may serve as potential biomarkers for further research in Alzheimer's disease.
Background Alzheimer's disease (AD) is a heterogeneous neurodegenerative disease with complex pathophysiology. Therefore, the identification of novel effective fluid biomarkers is essential for Alzheimer's disease diagnosis and drug development. This study aimed to identify potential candidate hub proteins in cerebrospinal fluid for precise Alzheimer's disease diagnosis using bioinformatics methods. Methods A total of 29 co-significant differentially expressed proteins were identified by differential protein expression analysis in four different cohorts. Functional enrichment analysis revealed that most of these proteins were enriched in pathways related to glycometabolism. Using the Least Absolute Shrinkage and Selection Operator (LASSO) and random forest feature selection methods, six hub proteins [14-3-3 protein zeta/delta (YWHAZ), SPARC-related modular calcium-binding protein 1 (SMOC1), aldolase A (ALDOA), pyruvate kinase isoenzyme type M2 (PKM), chitinase-3-like protein 1 (CHI3L1), and secreted phosphoprotein 1 (SPP1)] were identified. Results These six hub proteins were upregulated in the cerebrospinal fluid of patients with Alzheimer's disease compared with cognitively unimpaired control individuals. Meanwhile, SMOC1, ALDOA, and PKM were specifically upregulated in the cerebrospinal fluid of patients with Alzheimer's disease but not in other neurodegenerative diseases. Build AD diagnostic models showed that a single hub protein or six hub proteins combination had an excellent ability to discriminate Alzheimer's disease. Conclusions In conclusion, our study suggests that these identified hub proteins, which are related to glycometabolism, may be potential biomarkers for further basic and clinical research in Alzheimer's disease.

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