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pmid:36440267

Identification of hub genes of Parkinson's disease through bioinformatics analysis.

Yajun Yang · Yi Wang · Ce Wang · Xinjuan Xu · Cai Liu · Xintao Huang

Frontiers in neuroscience · 2022 doi:10.3389/fnins.2022.974838

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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title
Identification of hub genes of Parkinson's disease through bioinformatics analysis.
doi
10.3389/fnins.2022.974838
pmid
36440267
authors array · 6 items
[0]
Yajun Yang
[1]
Yi Wang
[2]
Ce Wang
[3]
Xinjuan Xu
[4]
Cai Liu
[5]
Xintao Huang
journal
Frontiers in neuroscience
year
2022
abstract
Parkinson's disease (PD) is a common neurodegenerative disease, and there is still a lack of effective diagnostic and treatment methods. This study aimed to search for hub genes that might serve as diagnostic or therapeutic targets for PD. All the analysis was performed in R software. The expression profile data of PD (number: GSE7621) was acquired from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) associated with PD were screened by the "Limma" package of the R software. Key genes associated with PD were screened by the "WGCNA" package of the R software. Target genes were screened by merging the results of "Limma" and "WGCNA." Enrichment analysis of target genes was performed by Gene Ontology (GO), Disease Ontology (DO), and Kyoto Enrichment of Genes and Genomes (KEGG). Machine learning algorithms were employed to screen for hub genes. Nomogram was constructed using the "rms" package. And the receiver operating characteristic curve (ROC) was plotted to detect and validate our prediction model sensitivity and specificity. Additional expression profile data of PD (number: GSE20141) was acquired from the GEO database to validate the nomogram. GSEA was used to determine the biological functions of the hub genes. Finally, RPL3L, PLEK2, PYCRL, CD99P1, LOC100133130, MELK, LINC01101, and DLG3-AS1 were identified as hub genes of PD. These findings can provide a new direction for the diagnosis and treatment of PD.
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The “Limma” R package was used to screen DEGs between PD and normal samples, and genes with P < 0.05 and |log2FC| >1 were regarded as DEGs (Liu et al., 2021).
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The “Limma” R package was used to screen DEGs between PD and normal samples, and genes with P < 0.05 and |log2FC| >1 were regarded as DEGs (Liu et al., 2021).
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Using Limma differential-expression screening, WGCNA, and machine-learning analyses of GEO expression data, the study identified eight PD hub genes and developed a diagnostic nomogram with AUC values of 1.000 in GSE7621 and 0.900 in GSE20141.
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Finally, eight common potential genes, namely, RPL3L, PLEK2, PYCRL, CD99P1, LOC100133130, MELK, LINC01101, and DLG3-AS1, were regarded as the hub genes of PD patients using the above three algorithms (Figure 4D).
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sections[16] "Establishment of diagnostic nomogram for PD" paragraph 2
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The area under the curve (AUC) of the GSE7621 dataset was 1.000 (Figure 5B), and that of the GSE20141 dataset was 0.900 (Figure 5C).
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