The Exon-Based Transcriptomic Analysis of Parkinson’s Disease

Parkinson's disease (PD) is a neurodegenerative disease with a complicated pathophysiology and diagnostics. Blood-based whole transcriptome analysis of the longitudinal PPMI cohort was performed with a focus on the change in the expression of exons to find potential RNA-based biomarkers. At the moment of diagnosis, the expression of exons was very similar in both control and PD patients. The exon-based analysis identified 27 differentially expressed exons in PD patients three years after the diagnosis compared to the health controls. Moreover, thirteen exons were differentially expressed during the three-year progression of the PD. At the same time, control subjects had only minimal changes that can mostly be attributed to being related to aging. Differentially regulated exons we identified in the PD cohort were mostly related to different aspects of the pathophysiology of PD, such as an innate immune response or lysosomal activity. We also observed a decline in the expression of the <i>OPN1MW3</i> gene that is related to colour vision, which suggests that colour vision analysis could be a practical biomarker to monitor the progression of PD.

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Publication Details

Journal
Biomolecules
Published
2025-03-19
DOI
https://doi.org/10.3390/biom15030440
Citations
2
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
1.61

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article

The Exon-Based Transcriptomic Analysis of Parkinson’s Disease

Sulev Kõks
2 citations
Biomolecules
RNA regulation and disease
1.61
article

The Exon-Based Transcriptomic Analysis of Parkinson’s Disease

Sulev Kõks
article en
2 citations

Abstract

Parkinson's disease (PD) is a neurodegenerative disease with a complicated pathophysiology and diagnostics. Blood-based whole transcriptome analysis of the longitudinal PPMI cohort was performed with a focus on the change in the expression of exons to find potential RNA-based biomarkers. At the moment of diagnosis, the expression of exons was very similar in both control and PD patients. The exon-based analysis identified 27 differentially expressed exons in PD patients three years after the diagnosis compared to the health controls. Moreover, thirteen exons were differentially expressed during the three-year progression of the PD. At the same time, control subjects had only minimal changes that can mostly be attributed to being related to aging. Differentially regulated exons we identified in the PD cohort were mostly related to different aspects of the pathophysiology of PD, such as an innate immune response or lysosomal activity. We also observed a decline in the expression of the <i>OPN1MW3</i> gene that is related to colour vision, which suggests that colour vision analysis could be a practical biomarker to monitor the progression of PD.

BiomoleculesVol. 15(3)
Murdoch University (AU), Perron Institute for Neurological and Translational Science (AU), Avenir Health (US)
Perron Institute for Neurological and Translational Science
Good health and well-being
Openalex Percentile: Top 18%
RNA regulation and disease
1.61
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