Gene expression signatures, pathways and networks in carotid atherosclerosis

• Published in: Journal of internal medicine Vol. 279; no. 3; pp. 293 - 308
• Main Authors: Perisic, L., Aldi, S., Sun, Y., Folkersen, L., Razuvaev, A., Roy, J., Lengquist, M., Åkesson, S., Wheelock, C. E., Maegdefessel, L., Gabrielsen, A., Odeberg, J., Hansson, G. K., Paulsson‐Berne, G., Hedin, U.
• Format: Journal Article
• Language: English
• Published: England 01.03.2016
• Subjects: Aged; atherosclerosis; Carotid Artery Diseases - genetics; carotid plaques; Female; gene expression; Gene Regulatory Networks; Humans; Male; Medicin och hälsovetenskap; microarrays; Signal Transduction; Transcriptome; atherosclerosis; carotid plaques; gene expression; microarrays
• ISSN: 0954-6820; 1365-2796; 1365-2796
• DOI: 10.1111/joim.12448

Background Embolism from unstable atheromas in the carotid bifurcation is a major cause of stroke. Here, we analysed gene expression in endarterectomies from patients with symptomatic (S) and asymptomatic (AS) carotid stenosis to identify pathways linked to plaque instability. Methods Microarrays were prepared from plaques (n = 127) and peripheral blood samples (n = 96) of S and AS patients. Gene set enrichment, pathway mapping and network analyses of differentially expressed genes were performed. Results These studies revealed upregulation of haemoglobin metabolism (P = 2.20E‐05) and bone resorption (P = 9.63E‐04) in S patients. Analysis of subgroups of patients indicated enrichment of calcification and osteoblast differentiation in S patients on statins, as well as inflammation and apoptosis in plaques removed >1 month compared to <2 weeks after symptom. By prediction profiling, a panel of 30 genes, mostly transcription factors, discriminated between plaques from S versus AS patients with 78% accuracy. By meta‐analysis, common gene networks associated with atherosclerosis mapped to hypoxia, chemokines, calcification, actin cytoskeleton and extracellular matrix. A set of dysregulated genes (LMOD1, SYNPO2, PLIN2 and PPBP) previously not described in atherosclerosis were identified from microarrays and validated by quantitative PCR and immunohistochemistry. Conclusions Our findings confirmed a central role for inflammation and proteases in plaque instability, and highlighted haemoglobin metabolism and bone resorption as important pathways. Subgroup analysis suggested prolonged inflammation following the symptoms of plaque instability and calcification as a possible stabilizing mechanism by statins. In addition, transcriptional regulation may play an important role in the determination of plaque phenotype. The results from this study will serve as a basis for further exploration of molecular signatures in carotid atherosclerosis.