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CT hyperdense cerebral artery sign reflects distinct proteomic composition in acute ischemic stroke thrombus

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BMJ PUBLISHING GROUP
DOI: 10.1136/jnis-2022-019937

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CT; thrombectomy; CT angiography; stroke

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This study used mass spectrometry to analyze the protein composition of thrombi in 24 patients with acute ischemic stroke. It found that thrombi with hyperdense cerebral artery sign (HCAS) had specific differential protein abundance, while thrombi without HCAS were enriched in certain proteins such as soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein and tyrosine-protein kinase Fyn. In addition, thrombi without HCAS were also enriched in biological processes involving plasma lipoprotein and protein-lipid remodeling/assembling, and lipoprotein metabolic processes, as well as cellular components including mitochondria. These findings suggest that HCAS reflects distinct proteomic composition in AIS thrombus.
BackgroundHyperdense cerebral artery sign (HCAS) is an imaging biomarker in acute ischemic stroke (AIS) that has been shown to be associated with various clinical outcomes and stroke etiology. While prior studies have correlated HCAS with histopathological composition of cerebral thrombus, it is unknown whether and to what extent HCAS is also associated with distinct clot protein composition. MethodsThromboembolic material from 24 patients with AIS were retrieved via mechanical thrombectomy and evaluated with mass spectrometry in order to characterize their proteomic composition. Presence (+) or absence (-) of HCAS on preintervention non-contrast head CT was then determined and correlated with thrombus protein signature with abundance of individual proteins calculated as a function HCAS status. Results24 clots with 1797 distinct proteins in total were identified. 14 patients were HCAS(+) and 10 were HCAS(-). HCAS(+) were most significantly differentially abundant in actin cytoskeletal protein (P=0.002, Z=2.82), bleomycin hydrolase (P=0.007, Z=2.44), arachidonate 12-lipoxygenase (P=0.004, Z=2.60), and lysophospholipase D (P=0.007, Z=2.44), among other proteins; HCAS(-) clots were differentially enriched in soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (P=0.0009, Z=3.11), tyrosine-protein kinase Fyn (P=0.002, Z=2.84), and several complement proteins (P<0.05, Z>1.71 for all), among numerous other proteins. Additionally, HCAS(-) thrombi were enriched in biological processes involved with plasma lipoprotein and protein-lipid remodeling/assembling, and lipoprotein metabolic processes (P<0.001), as well as cellular components including mitochondria (P<0.001). ConclusionsHCAS is reflective of distinct proteomic composition in AIS thrombus. These findings suggest that imaging can be used to identify mechanisms of clot formation or maintenance at the protein level, and might inform future research on thrombus biology and imaging characterization.

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