Abstract

We evaluated the reliability of 8-hydroxy-2′-deoxyguanosine (8-OHdG), and determined its ability to predict functional outcomes in stroke survivors. The rehabilitation effect on 8-OHdG and functional outcomes were also assessed. Sixty-one stroke patients received a 4-week rehabilitation. Urinary 8-OHdG levels were determined by liquid chromatography–tandem mass spectrometry. The test-retest reliability of 8-OHdG was good (interclass correlation coefficient = 0.76). Upper-limb motor function and muscle power determined by the Fugl-Meyer Assessment (FMA) and Medical Research Council (MRC) scales before rehabilitation showed significant negative correlation with 8-OHdG (r = −0.38, r = −0.30; p < 0.05). After rehabilitation, we found a fair and significant correlation between 8-OHdG and FMA (r = −0.34) and 8-OHdG and pain (r = 0.26, p < 0.05). Baseline 8-OHdG was significantly correlated with post-treatment FMA, MRC, and pain scores (r = −0.34, −0.31, and 0.25; p < 0.05), indicating its ability to predict functional outcomes. 8-OHdG levels were significantly decreased, and functional outcomes were improved after rehabilitation. The exploratory study findings conclude that 8-OHdG is a reliable and promising biomarker of oxidative stress and could be a valid predictor of functional outcomes in patients. Monitoring of behavioral indicators along with biomarkers may have crucial benefits in translational stroke research.

Highlights

  • Biomarkers of oxidative stress are defined as a biological molecule whose chemical structure has been modified by free radicals [1]

  • Our study has delineated for the first time the correlation between 8-OHdG and functional outcomes in stroke rehabilitation

  • The findings demonstrated that higher baseline 8-OHdG content represents poor functional outcomes, whereas lower 8-OHdG after rehabilitation resulted in improved functional outcomes

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Summary

Introduction

Biomarkers of oxidative stress are defined as a biological molecule whose chemical structure has been modified by free radicals [1]. Because of the difficulties in measuring unstable free radicals in human samples, the degree of oxidative stress can be determined by measuring the stable end-products of oxidatively modified proteins, lipids, and DNA [5]. The most sensitive biomarker to determine oxidative DNA damage is 8-hydroxy-2'-deoxyguanosine (8-OHdG). Elevated urinary 8-OHdG content released from the brain is closely correlated with the prognosis of stroke [2,6]. Levels of 8-OHdG may reflect the severity of stroke and are associated with functional disabilities

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