Immune-inflammatory markers and arterial stiffness indexes in subjects with acute ischemic stroke.
- Autori: DI RAIMONDO, D.; Pecoraro, R.; Serio, A.; D'Aguanno, G.; Pinto, A.; Licata, G.; Tuttolomondo, A.
- Anno di pubblicazione: 2010
- Tipologia: Articolo in rivista (Articolo in rivista)
- Parole Chiave: ischemic stroke, arterial stiffness
- OA Link: http://hdl.handle.net/10447/57515
No study has yet evaluated the relationship between arterial stiffness indexes and immuno-inflammatory pathway in patients with an acute cardiovascular or cerebrovascular event. The aim of our study was to evaluate in patients with acute ischemic stroke the relationship between immune-inflammatory markers and arterial stiffness indexes. METHODS: 107 subjects with acute ischemic stroke and 107 controls without stroke. We evaluated plasma levels of C-reactive protein (CRP), interleukin-1beta (IL-1β), tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6) and interleukin-10 (IL-10), E-selectin, P-selectin, intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), von Willebrand Factor (vWF), tissue plasminogen activator (TPA), plasminogen activator inhibitor-1 (PAI-1). Carotid-femoral pulse wave velocity (PWV) and augmentation index (Aix) were evaluated. RESULTS: There was a significant positive relationship, corrected for age, and gender, between PWV and CRP, TNF-α, IL1β, VWF and IL-6. Aix was significantly related to VWF, IL-6 and TNF-α levels. Among Lacunar subtype PWV was significantly related to CRP, IL-1β, IL-6, TNF-α and vWF. In LAAS subjects PWV was significantly related to CRP, IL-1β, IL-6, TNF-α but not with vWF. Among CEI subtype, PWV was significantly and positively related to CRP, IL-1β, TNF-α and vWF. DISCUSSION: Our findings show that both aortic stiffness and wave reflection are related to the degree of systemic inflammation in stroke subjects, suggesting that circulating inflammation mediators can influence the stiffness of vessels distant to those involved in the disease process itself.