# VGF AQEE- and GGEE-peptides differentiate between dementia types

**Authors:** B. Noli, B. Muqaku, M. Gouda, AL. Manai, M. Nagl, S. Anderl-Straub, L. Werner, M. Otto, C. E. Teunissen, P. Oeckl, C. Cocco

PMC · DOI: 10.1007/s00415-025-13441-1 · Journal of Neurology · 2025-11-04

## TL;DR

Researchers found that specific peptides from a brain protein can help distinguish between different types of dementia, like Alzheimer's and dementia with Lewy bodies.

## Contribution

The study confirms and extends the diagnostic potential of AQEE-10 and GGEE peptides in differentiating dementia with Lewy bodies from Alzheimer's disease and controls.

## Key findings

- AQEE-10 levels were significantly reduced in dementia with Lewy bodies compared to Alzheimer's and controls.
- Both AQEE-10 and GGEE levels showed strong diagnostic accuracy for dementia with Lewy bodies.
- AQEE-10 and GGEE concentrations were positively correlated in cerebrospinal fluid samples.

## Abstract

Alzheimer’s disease (AD) and dementia with Lewy bodies (DLB) are neurodegenerative disorders with overlapping clinical features, making differential diagnosis challenging. The AQEE and GGEE peptides, derived from the proVGF neuroprotein, have emerged as potential cerebrospinal fluid (CSF) biomarkers for dementia. Indeed, we previously observed a reduction in AQEE-10 levels using selected reaction monitoring (SRM) and GGEE levels using enzyme-linked immunosorbent assay (ELISA) in a cohort of DLB patients compared to both controls and AD patients. To better investigate the diagnostic utility of these peptides, we analyzed CSF samples from both the original cohort and a newly recruited cohort. The new cohort (cohort 1) included patients, from Ulm University Hospital, with Parkinson’s disease dementia (PDD) and DLB (combined as PDD/DLB; n = 18), and AD (n = 19). The previously analyzed cohort (cohort 2), from the Amsterdam University Medical Center, included DLB (n = 44), AD (n = 20), and cognitively healthy controls (n = 22). AQEE-10 levels were quantified by multiple reaction monitoring (MRM) in cohort 1 and by ELISA in both cohorts. GGEE levels were measured by ELISA in cohort 1 to corroborate and extend previous findings. MRM-based analysis revealed a significant reduction of AQEE-10 levels in DLB compared to both controls and AD (p < 0.05; ROC-AUC: 78% and 82%, respectively). This finding was confirmed by ELISA, for both AQEE-10 and GGEE peptide levels, along with a positive correlation between their concentrations. These results support AQEE-10 and GGEE as promising peptide biomarkers for distinguishing DLB from other dementia.

The online version contains supplementary material available at 10.1007/s00415-025-13441-1.

## Linked entities

- **Proteins:** VGF (VGF nerve growth factor inducible)
- **Diseases:** Alzheimer’s disease (MONDO:0004975), dementia with Lewy bodies (MONDO:0007488)

## Full-text entities

- **Diseases:** DLB (MESH:D020961), neurodegenerative disorders (MESH:D019636), dementia (MESH:D003704), PDD (MESH:D010300), AD (MESH:D000544)
- **Chemicals:** AQEE-10 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12586231