Folia Neuropathologica · 2022 · 18 citations · 26 references
Life SciencesNeurologyNeuroscienceClinical NeuroscienceCognitive NeurologyNeuropathologyCerebrovascular DiseaseCognitive ImpairmentMicrorna BiologyNeurological AssessmentNeuropsychological AssessmentStrokeCirculating Microrna DetectionCirculating MicrornasComparative Diagnostic PerformanceDiagnostic Performance MetricsMicrorna BiomarkersStroke BiomarkersStroke Severity AssessmentStroke-related Cognitive Impairment
INTRODUCTION: The diagnosis of post-stroke cognitive impairment (PSCI) mainly depends on neuro-psychological evaluation. It still lacks a sensitive and objective diagnostic biomarker. MicroRNAs (miRNAs, miRs) are novel and potential disease biomarkers. Our aim was to detect which specific miRNA is a good diagnostic biomarker for PSCI. MATERIAL AND METHODS: There were 77 first-ever stroke patients enrolled. Blood samples were collected at 14 days after stroke. Level of serum miR-21, miR-124, miR-132, and miR-200b were determined by quantitative polymerase chain reaction. Mini-mental state examination (MMSE) scale was used to measure the cognitive function of patients. Factional anisotropy (FA) score of diffusion tensor imaging was applied to detect the alteration of white matter. In addition, the relationship between miRNA level and cognitive status was further explored by correlation analysis. RESULTS: Finally, 45 PSCI and 32 post-stroke cognitive normality (PSCN) patients were enrolled. The expression of miR-21, miR-132, and miR-200b in PSCI patients was higher than in PSCN patients. In particular, the miR-21 level was substantially correlated with MMSE scores (r = 0.752, p < 0.001) and FA value (r = 0.636, p < 0.001). Additionally, the diagnostic performance of miR-21 alone or the combination of miR-21 and FA values performed well. CONCLUSIONS: The miR-21 alone or combination of miR-21 and FA values are valuable diagnostic biomarkers in discriminating PSCI from PSCN.
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