Abstract

Introduction: Plasma oxidized human serum albumin (OxHSA) is evidence of an active antioxidant mechanism as measured by oxidized species of HSA. CXCL-10 is a pro-inflammatory chemokine associated with ischemic conditions. Accordingly, we examined the relationship of admission OxHSA and CXCL-10 with discharge mRS in acute ischemic stroke (AIS).Methods: Plasma samples and clinical data were collected prospectively at a Comprehensive Stroke Center. Admission biomarkers of oxidative stress, CXCL-10 and %OxHSA, were measured. We examined if CXCL-10 or %OxHSA correlated with age, admission NIHSS score, and discharge mRS score using Spearman's Rank correlation. Logistic regression was performed to identify independent predictors of a favorable discharge mRS (≤2).Results: In 106 consecutive AIS patients, the median age was 73 (IQR 61–84), 47% were male, and the median admission NIHSS score was 11 (IQR 5–19). %OxHSA and CXCL-10 were significantly correlated (r = 0.23, p = 0.02). Both biomarkers were significantly correlated with age: %OxHSA (r = 0.44, p < 0.001) and CXCL-10 (r = 0.32, p = 0.001). Neither biomarker was correlated with admission NIHSS. There was a borderline significant correlation with discharge mRS and %OxHSA (r = −0.17, p = 0.08), where higher %OxHSA correlated with lower discharge mRS scores. For every 1% increase in %OxHSA, the odds of a favorable discharge mRS increased 11%. The odds of a favorable discharge mRS decreased 18% for every 1-point increase in the initial NIHSS.Conclusions: OxHSA, the result of an oxidative environment and evidence of the strong antioxidant buffering capacity of HSA, correlated with CXCL-10 and discharge mRS, implying that strong antioxidant activity of albumin may confer better outcomes.

Highlights

  • Plasma oxidized human serum albumin (OxHSA) is evidence of an active antioxidant mechanism as measured by oxidized species of HSA

  • The ability to quench free radicals by scavenger molecules such as HSA is crucial in preventing the oxidation of key macromolecules. These results suggest plasma CXCL10 represents a general marker of inflammation and oxidative stress and is not predictive of loss of function or disability in acute ischemic stroke (AIS)

  • Higher amounts of OxHSA correlated with better outcomes in AIS patients based on modified Rankin Scale (mRS) scores

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Summary

Introduction

Plasma oxidized human serum albumin (OxHSA) is evidence of an active antioxidant mechanism as measured by oxidized species of HSA. We examined the relationship of admission OxHSA and CXCL-10 with discharge mRS in acute ischemic stroke (AIS). Acute ischemic stroke (AIS) is a serious health condition characterized by inadequate brain blood perfusion due to a blockage resulting in rapid loss of neurological function. Reperfusion injury results in the reintroduction of oxygenated blood to the ischemic regions of the brain. This can induce biochemical pathways that produce reactive oxygen species (ROS) and pro-inflammatory mediators potentially leading to apoptosis and cellular necrosis [1]. Additional cellular targets include proteins which are susceptible to oxidative damage following reperfusion leading to immune system activation, neutrophil recruitment, and neurovascular inflammation [3]. Protein oxidation is positively correlated with complications following AIS such as post-stroke depression resulting in increased rehabilitation times, disability/cognitive impairment, and mortality [4]

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