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◆ Scientific Reports2026-09-01· Medicine

VEGFA gene expression levels in patients with Parkinson’s disease and first-degree relatives

Eva Augste, K. Smešný Trtková, K. Feichtingerová, A. Kochanová, Jiří Kozel, Patricie Michalčová, F. Pergler, T. Mičaník, R. Holý, Z. Hamdi, P. Dušek, Dana Šalounová, D. Školoudík, Petra Bártová

原始摘要(英文原文)· Original abstract
Abstract Background: Vascular endothelial growth factor A (VEGFA) contributes to angiogenesis and exerts neurotrophic and neuroprotective effects. Altered VEGFA expression has been implicated in neurodegenerative processes, including Parkinson´s disease (PD), yet findings from peripheral transcriptomic studies remain inconsistent. Data on individuals at increased risk, particularly first-degree relatives (FDRs), are limited. Objective: To evaluate peripheral blood VEGFA mRNA expression in patients with PD and their asymptomatic FDRs compared with healthy controls, and to assess age-related patterns and diagnostic performance. Methods: Peripheral blood VEGFA expression was analyzed in 123 participants (PD patients, FDRs, healthy controls) using one-step RT-qPCR normalized to B2M . Relative expression values were log-transformed (logVEGFA). Group differences, age correlations, and diagnostic discrimination were assessed using ANOVA, Pearson correlation, and receiver operating characteristic (ROC) analysis. Results: Both PD patients and FDRs showed significantly higher logVEGFA levels than healthy controls (p = 0.004), with the most pronounced differences observed in participants aged ≤ 60 years (p < 0.001). A positive correlation between age and logVEGFA was detected only in healthy controls. In participants aged ≤ 60 years, logVEGFA demonstrated excellent discrimination between PD patients and healthy individuals (AUC 0.897; 95% CI 0.771–1.000; sensitivity 100%, specificity 73.3%). Conclusions: Peripheral VEGFA expression is elevated in both PD patients and FDRs, particularly in younger individuals. Age-stratified VEGFA assessment may support early identification of individuals at risk of PD and complement existing prodromal biomarkers, pending longitudinal validation.
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