Archive 24/11/25

A new glycan marker for depressive disorder

A group from Division of Neuropsychiatry, Department of Neuroscience, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan has reported about a new glycan marker for predicting depressive disorder.
https://www.nature.com/articles/s41598-024-80507-x

It was found that plasma extracellular vesicles (EVs) containing WGA-binding von Willebrand factor (vWF) (WGA-vWF) could be a diagnostic marker for the diagnosis of patients with major depressive disorder (MDD) in a depressive state regardless of gender and age.

WGA-vWF expression was significantly lower in plasma EVs of patients with MDD in a depressive state than those of healthy control participants (HCs). ROC analysis indicated that the AUC value for the diagnosis was 0.92 (95% CI 0.82–1.00) between patients with MDD and HCs. Furthermore, WGA-vWF expression remarkably increased from depressive to remission processes. With using this result, it was possible to distinguish between patients with MDD in depressive and remission states (AUC of 0.98, 95% CI 0.93–1.00).

Bisecting GlcNAc could be an early Alzheimer’s disease biomarker

A group from Division of Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Karolinska Institutet, Sweden has reported about a new glyca marker, bisecting GlcNAc, which is able to predict cognitive decline in amyloid- and tau-negative patients.
https://academic.oup.com/braincomms/article/6/6/fcae371/7826117?login=false

This is a reprt about an early biomarker for Alzheimer’s disease.

In Alzheimer’s disease, it has been known that an increased accumulation and aggregation of amyloid β-peptide (Aβ) causes amyloid formation in the brain followed by phosphorylation of tau and neurodegeneration and cognitive decline. In this study, it was found that Bisecting GlcNAc could be an early Alzheimer’s disease biomarker, which is able to predict cognitive decline already at an amyloid-/tau-negative stage.

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