Whole blood transcript and protein abundance of the vascular endothelial growth factor family relate to cognitive performance

•We describe a novel association between blood VEGF expression levels and memory.•We describe a novel association between blood VEGF protein levels and AD pathology biomarkers.•Expression and proteins levels of VEGF in blood are potential biomarkers of AD. The vascular endothelial growth factor (VEG...

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Veröffentlicht in:Neurobiology of aging 2023-04, Vol.124, p.11-17
Hauptverfasser: Libby, Julia B., Seto, Mabel, Khan, Omair A., Liu, Dandan, Petyuk, Vlad, Oliver, Nekesa C., Choi, Min Ji, Whitaker, Marsalas, Patterson, Khiry L., Arul, Albert B., Gifford, Katherine A., Blennow, Kaj, Zetterberg, Henrik, Dumitrescu, Logan, Robinson, Renã AS, Jefferson, Angela L., Hohman, Timothy J.
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Sprache:eng
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Zusammenfassung:•We describe a novel association between blood VEGF expression levels and memory.•We describe a novel association between blood VEGF protein levels and AD pathology biomarkers.•Expression and proteins levels of VEGF in blood are potential biomarkers of AD. The vascular endothelial growth factor (VEGF) family of genes has been implicated in the clinical development of Alzheimer's Disease (AD). A previous study identified associations between gene expression of VEGF family members in the prefrontal cortex and cognitive performance and AD pathology. This study explored if those associations were also observed in the blood. Consistent with previous observations in brain tissue, higher blood gene expression of placental growth factor (PGF) was associated with a faster rate of memory decline (p=0.04). Higher protein abundance of FMS-related receptor tyrosine kinase 4 (FLT4) in blood was associated with biomarker levels indicative of lower amyloid and tau pathology, opposite the direction observed in brain. Also, higher gene expression of VEGFB in blood was associated with better baseline memory (p=0.008). Notably, we observed that higher gene expression of VEGFB in blood was associated with lower expression of VEGFB in the brain (r=-0.19, p=0.02). Together, these results suggest that the VEGFB, FLT4, and PGF alterations in the AD brain may be detectable in the blood compartment.
ISSN:0197-4580
1558-1497
DOI:10.1016/j.neurobiolaging.2023.01.002