Peripheral Blood Gene Expression Profiling Reveals Molecular Pathways Associated with Cervical Artery Dissection.
Polina S ShlapakovaLarisa A DobryninaLudmila A KalashnikovaMariia V GubanovaMaria S DanilovaElena V GnedovskayaAnastasia P GrigorenkoFedor E GusevAndrey Dmitrievich ManakhovEvgeny I RogaevPublished in: International journal of molecular sciences (2024)
Cervical artery dissection (CeAD) is the primary cause of ischemic stroke in young adults. Monogenic heritable connective tissue diseases account for fewer than 5% of cases of CeAD. The remaining sporadic cases have known risk factors. The clinical, radiological, and histological characteristics of systemic vasculopathy and undifferentiated connective tissue dysplasia are present in up to 70% of individuals with sporadic CeAD. Genome-wide association studies identified CeAD-associated genetic variants in the non-coding genomic regions that may impact the gene transcription and RNA processing. However, global gene expression profile analysis has not yet been carried out for CeAD patients. We conducted bulk RNA sequencing and differential gene expression analysis to investigate the expression profile of protein-coding genes in the peripheral blood of 19 CeAD patients and 18 healthy volunteers. This was followed by functional annotation, heatmap clustering, reports on gene-disease associations and protein-protein interactions, as well as gene set enrichment analysis. We found potential correlations between CeAD and the dysregulation of genes linked to nucleolar stress, senescence-associated secretory phenotype, mitochondrial malfunction, and epithelial-mesenchymal plasticity.
Keyphrases
- genome wide identification
- genome wide
- peripheral blood
- copy number
- gene expression
- end stage renal disease
- young adults
- risk factors
- ejection fraction
- newly diagnosed
- transcription factor
- single cell
- dna methylation
- genome wide analysis
- peritoneal dialysis
- prognostic factors
- oxidative stress
- bone marrow
- genome wide association
- late onset
- dna damage
- risk assessment
- endothelial cells
- rna seq
- small molecule
- amyotrophic lateral sclerosis
- drug induced
- case control