Abstract

Elevated red blood cell distribution width (RDW) has been found to be associated with the occurrence of ischemic stroke. However, there is no defined relationship between RDW and neuronal damage in acute ischemic stroke (AIS). This study was designed to determine the relationship between RDW and neuronal damage in AIS patients. A total of 442 consecutive AIS patients from January 2018 to June 2019 were evaluated for neuronal damage, which was estimated by serum neuron-specific enolase (NSE) levels. Red blood cell distribution width-standard deviation (RDW-SD), a parameter that reflects the heterogeneity of red blood cell volume, was also assessed. We evaluated the association between the RDW-SD and serum NSE level through multivariate-adjusted linear regression analysis. Both the serum NSE level and the incidence of high NSE increased according to the increased RDW-SD tertile in AIS patients (p<0.01). There was a positive correlation between RDW-SD and serum NSE levels (r=0.275, 95% CI: 0.187-0.359, p<0.001). The beta coefficients (95% CI) between RDW-SD and serum NSE levels were 0.32 (0.21-0.42, p<0.001) and 0.26 (0.15-0.38, p<0.001), respectively, in AIS patients before and after adjusting for potential confounders. In conclusion, we found a significant positive association between RDW-SD and neuronal damage in AIS patients.

Highlights

  • The red blood cell volume distribution width (RDW) is a parameter reflecting the volume heterogeneity of peripheral blood red blood cells [1]

  • Those who had missing data related to serum neuron-specific enolase (NSE), red blood cell distribution width (RDW)-SD, sex and age were excluded from the eligible candidates for this study (n=51)

  • Our study found a positive correlation between the Red blood cell distribution width-standard deviation (RDW-SD) and serum NSE level, and the NSE level and incidence of high NSE were increased with graded RDW-SD in both genders

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Summary

INTRODUCTION

The red blood cell volume distribution width (RDW) is a parameter reflecting the volume heterogeneity of peripheral blood red blood cells [1]. Several previous studies have www.aging-us.com suggested that serum NSE is associated with infarction volume, worse outcome, hemorrhagic transformation, and other neurological and neuroendocrine diseases [10,11,12,13]. The association between RDW-SD and serum NSE levels remain unclear in the AIS population, and whether elevated RDW-SD levels are an important risk factor for serum NSE in the AIS population needs to be further investigated. We conducted this cross-sectional study, aiming to assess the association between RDWSD and serum NSE levels in the AIS population. No study has previously examined the association between the RDW-SD level and serum NSE in the AIS population

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