Cited by 35Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCerebrospinal fluid and hydrocephalus

VGF in Cerebrospinal Fluid Combined With Conventional Biomarkers Enhances Prediction of Conversion From MCI to AD

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Llano, Daniel A., Devanarayan, Priya, Devanarayan, Viswanath·2019·Alzheimer Disease & Associated Disorders

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Abstract

BACKGROUND: Previous work has suggested that the brain and cerebrospinal fluid (CSF) levels of a neural protein involved in synaptic transmission, VGF (a noninitialism), may be altered in mild cognitive impairment (MCI) and Alzheimer Disease (AD). The objective of the current work is to examine the potential of CSF levels of a peptide derived from VGF to predict conversion from MCI to AD. MATERIALS AND METHODS: Using multivariate analytical approaches, the performance of the conventional biomarkers (CSF Aβ1-42 and phosphorylated tau +/- hippocampal volume) was compared with the same biomarkers combined with CSF VGF peptide levels in a large publicly available data set from human subjects. RESULTS: It was observed that VGF peptides are lowered in CSF of patients with AD compared with controls and that combinations of CSF Aβ1-42 and phosphorylated tau, hippocampal volume, and VGF peptide levels outperformed conventional biomarkers alone (hazard ratio=2.2 vs. 3.9), for predicting MCI to AD conversion. CONCLUSIONS: CSF VGF enhances the ability of conventional biomarkers to predict MCI to AD conversion. Future work will be needed to determine the specificity of VGF for AD versus other neurodegenerative diseases.

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Crossref · 10.1097/wad.0000000000000328

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Authors
Llano, D. A., Devanarayan, P., & Devanarayan, V.
Affiliations
  • University of Illinois Urbana-Champaign (US)
  • Souderton Area High School, Souderton
  • University of Illinois Chicago (US)
Corresponding author
Llano, Daniel A.
Venue
Alzheimer Disease & Associated Disorders
Published
2019-10
Volume
33
Issue
4
Pages
307-314
ISSN
0893-0341 (ISSN-L)
OpenAlex
W2957495611
Cited by
35
References
93
Citations by year
2026: 2 · 2025: 5 · 2024: 3 · 2023: 6 · 2022: 8 · 2021: 2 · 2020: 7 · 2019: 2
FWCI
3.78
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Alzheimer Disease & Associated Disorders (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Defense (U01 AG024904, W81XWH, W81XWH-12-2-, W81XWH-12, AG024904)
  • Alzheimer's Association (U01 AG024904, W81XWH-12-2-0012)
  • Biogen (W81XWH-12-2-0012, U01 AG024904, AG024904)
  • Alzheimer's Disease Neuroimaging Initiative (W81XWH-12-2–0012, U01AG024904, AG024904, W81XWH-12-2-)
  • BioClinica (U01 AG024904, W81XWH-12-2-0012, AG024904)
  • National Institutes of Health (W81XWH, W81XWH-12-2-0012, U01-AG024904, AG024904)
  • University of California, Davis
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
Keywords
VGF, cerebrospinal fluid biomarkers, mild cognitive impairment, Alzheimer's disease, conversion prediction, amyloid-beta 42, phosphorylated tau, hippocampal volume, combined biomarker detection, neurodegeneration
MeSH terms
Aged, Alzheimer Disease, Brain, Female, Hippocampus, Humans, Male, Peptide Fragments, Biomarkers, Amyloid beta-Peptides, tau Proteins, Disease Progression, Cognitive Dysfunction

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