Abstract
Background
The pathogenesis of development and rupture of intracranial aneurysms (IA) is largely unknown. Also, screening for IA to prevent aneurysmal subarachnoid hemorrhage (aSAH) is inefficient, as disease markers are lacking. We investigated gene expression profiles in blood of previous aSAH patients, who are still at risk for future IA, aiming to gain insight into the pathogenesis of IA and aSAH, and to make a first step towards improvement of aSAH risk prediction.
Methods and Results
We collected peripheral blood of 119 patients with aSAH at least two years prior, and 118 controls. We determined gene expression profiles using Illumina HumanHT-12v4 Bead-Chips. After quality control, we divided the dataset in a discovery (2/3) and replication set (1/ 3), identified differentially expressed genes, and applied (co-) differential co-expression to identify disease-related gene networks. No genes with a significant (false-discovery rate
Conclusions
No gene expression differences were present in blood of previous aSAH patients compared to controls, besides one differentially co-expressed gene network without a clear relevant biological function. Our findings suggest that gene expression profiles, as detected in blood of previous aSAH patients, do not reveal the pathogenesis of IA and aSAH, and cannot be used for aSAH risk prediction.
| Original language | English |
|---|---|
| Article number | e0139352 |
| Number of pages | 12 |
| Journal | PLoS ONE |
| Volume | 10 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 6-Oct-2015 |
Keywords
- GRAPH-THEORETICAL ANALYSIS
- INTRACRANIAL ANEURYSMS
- PERIPHERAL-BLOOD
- AORTIC-ANEURYSM
- BRAIN NETWORKS
- RISK-FACTORS
- LONG-TERM
- IDENTIFICATION
- METAANALYSIS
- BIOMARKERS
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