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Interleukin-10 facilitates the selection of patients for systemic thrombolysis.


ABSTRACT:

Background

Clinical-Diffusion mismatch (CDM; NIHSS score ?8 & DWI lesion volume ?25 mL) and Perfusion-Diffusion mismatch (PDM; difference >20% between initial DWI and MTT lesion volumes) have been proposed as surrogates for ischemic brains that are at risk of infarction. However, their utility to improve the selection of patients for thrombolytic treatment remains controversial. Our aim was to identify molecular biomarkers that can be used with neuroimaging to facilitate the selection of ischemic stroke patients for systemic thrombolysis.

Methods

We prospectively studied 595 patients with ischemic stroke within 12 h of the stroke onset. A total of 184 patients received thrombolytic treatment according to the SITS-MOST criteria. DWI and MTT volumes were measured at admission. The main outcome variable was good functional outcome at 3 months (modified Rankin scale <3). Serum levels of glutamate (Glu), IL-10, TNF-?, IL-6, NSE, and active MMP-9 also were determined at admission.

Results

Patients treated with t-PA who presented with PDM had higher IL-10 levels at admission (p?ConclusionsSerum levels of IL-10 facilitate the selection of ischemic stroke patients with CDM and PDM for systemic thrombolysis.

SUBMITTER: Rodriguez-Yanez M 

PROVIDER: S-EPMC3710209 | biostudies-literature | 2013 Jun

REPOSITORIES: biostudies-literature

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<h4>Background</h4>Clinical-Diffusion mismatch (CDM; NIHSS score ≥8 & DWI lesion volume ≤25 mL) and Perfusion-Diffusion mismatch (PDM; difference >20% between initial DWI and MTT lesion volumes) have been proposed as surrogates for ischemic brains that are at risk of infarction. However, their utility to improve the selection of patients for thrombolytic treatment remains controversial. Our aim was to identify molecular biomarkers that can be used with neuroimaging to facilitate the selection of  ...[more]

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