Abstract

BackgroundIschemic stroke patients are prone to infection by stroke-induced immunodepression. We hypothesized that levels of lipopolysaccharide binding protein (LBP), interleukin-10 (IL-10), IL-6 and C-reactive protein (CRP) are early predictors for the development of stroke-associated infection.MethodsFifty-six patients with ischemic stroke (n = 51) and transient ischemic attack (TIA) (n = 5) who presented within 6 hours after symptom onset and who were free of detectable infection on admission were included in the study. Of these, 20 developed early infections during the first week. Blood samples were taken at 6, 12, and 24 hours and at 3 and 7 days after stroke onset. Levels of LBP, Il-10, IL-6 and CRP, as well as S100B, were measured as markers of inflammation and brain damage by commercially available immunometric tests.ResultsIn the univariate analysis, levels of LBP, IL-10, IL-6 and CRP significantly differed between patients who developed an infection and those who did not. In the binary logistic regression analysis, which was adjusted for National Institutes of Health Stroke Scale (NIHSS) on admission, stroke subtype and S100B peak levels, as indicator of the extent of brain damage, IL-10 at 6 hours, CRP at 6 hours and NIHSS on admission were identified as independent predictors of infection (IL-10: P = 0.009; CRP: P = 0.018; NIHSS: P = 0.041). The area under the curve (AUC) of the receiver operating characteristic (ROC) curves in relation to the dichotomized status of the infection (infection versus no infection) was 0.74 (95% confidence interval: 0.59 to 0.88) for CRP at 6 hours, 0.76 (0.61 to 0.9) for IL-10 at 6 hours, 0.83 (0.71 to 0.94) for NIHSS on admission and 0.94 (0.88 to 1) for the combination of CRP, IL-10 and NIHSS. In a subanalysis, 16 patients with early infections were matched with 16 patients without infection according to S100B peak levels. Here, the temporal pattern of LBP, IL-10, IL-6 and CRP significantly differed between the patient groups.ConclusionsOur data show that blood levels of inflammation markers may be used as early predictors of stroke-associated infection. We propose prospective studies to investigate if the calculated cut-offs of CRP, IL-10 and NIHSS might help to identify patients who should receive early preventive antibiotic treatment.

Highlights

  • Ischemic stroke patients are prone to infection by stroke-induced immunodepression

  • Levels of lipopolysaccharide binding protein (LBP), IL-10, IL-6 and C-reactive protein (CRP) differed in patients with and without infection In the univariate analysis, levels of LBP, IL-10, IL-6 and CRP were compared between patients with and without infection (Table 2)

  • The analysis revealed that IL-10 at 6 h, CRP at 6 h and National Institutes of Health Stroke Scale (NIHSS) on admission are independently associated with infection (IL-10: P = 0.009; CRP: P = 0.018; NIHSS: P = 0.041) (Table 3)

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Summary

Introduction

We hypothesized that levels of lipopolysaccharide binding protein (LBP), interleukin-10 (IL-10), IL-6 and C-reactive protein (CRP) are early predictors for the development of stroke-associated infection. Infections occurring within the first week after stroke onset are regarded as strokeassociated. They are correlated with stroke severity, since, on the one hand, a severe neurological deficit may facilitate infection and on the other hand severe infections may trigger neurological worsening. Clinical studies found increased levels of the anti-inflammatory cytokine Interleukin-10 (IL-10) in patients with post-stroke infection [6,7]. Pro-inflammatory mediators such as C-reactive protein (CRP) and Interleukin-6 (IL-6) are increased in ischemic stroke patients who develop an infection [6,8]

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