Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis

Neurogranin (Ng) and visinin-like protein 1 (VILIP-1) are promising candidates for Alzheimer’s Disease (AD) biomarkers closely related to synaptic and neuronal degeneration. Both proteins are involved in calcium-mediated pathways. The meta-analysis was performed in random effects based on the ratio...

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Main Authors: Maciej Dulewicz, Agnieszka Kulczyńska-Przybik, Barbara Mroczko
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/21/8335
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author Maciej Dulewicz
Agnieszka Kulczyńska-Przybik
Barbara Mroczko
author_facet Maciej Dulewicz
Agnieszka Kulczyńska-Przybik
Barbara Mroczko
author_sort Maciej Dulewicz
collection DOAJ
description Neurogranin (Ng) and visinin-like protein 1 (VILIP-1) are promising candidates for Alzheimer’s Disease (AD) biomarkers closely related to synaptic and neuronal degeneration. Both proteins are involved in calcium-mediated pathways. The meta-analysis was performed in random effects based on the ratio of means (RoM) with calculated pooled effect size. The diagnostic utility of these proteins was examined in cerebrospinal fluid (CSF) of patients in different stages of AD compared to control (CTRL). Ng concentration was also checked in various groups with positive (+) and negative (-) amyloid beta (Aβ). Ng highest levels of RoM were observed in the AD (<i>n</i> = 1894) compared to CTRL (<i>n</i> = 2051) group (RoM: 1.62). Similarly, the VILIP-1 highest values of RoM were detected in the AD (<i>n</i> = 706) compared to CTRL (<i>n</i> = 862) group (RoM: 1.34). Concentrations of both proteins increased in more advanced stages of AD. However, Ng seems to be an earlier biomarker for the assessment of cognitive impairment. Ng appears to be related with amyloid beta, and the highest levels of Ng in CSF was observed in the group with pathological Aβ+ status. Our meta-analysis confirms that Ng and VILIP-1 can be useful CSF biomarkers in differential diagnosis and monitoring progression of cognitive decline. Although, an additional advantage of the protein concentration Ng is the possibility of using it to predict the risk of developing cognitive impairment in normal controls with pathological levels of Aβ1-42. Analyses in larger cohorts are needed, particularly concerning Aβ status.
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spelling doaj.art-1faf06ea6d664c2089a66029200336172023-11-20T20:01:56ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-11-012121833510.3390/ijms21218335Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-AnalysisMaciej Dulewicz0Agnieszka Kulczyńska-Przybik1Barbara Mroczko2Department of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-269 Bialystok, PolandDepartment of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-269 Bialystok, PolandDepartment of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-269 Bialystok, PolandNeurogranin (Ng) and visinin-like protein 1 (VILIP-1) are promising candidates for Alzheimer’s Disease (AD) biomarkers closely related to synaptic and neuronal degeneration. Both proteins are involved in calcium-mediated pathways. The meta-analysis was performed in random effects based on the ratio of means (RoM) with calculated pooled effect size. The diagnostic utility of these proteins was examined in cerebrospinal fluid (CSF) of patients in different stages of AD compared to control (CTRL). Ng concentration was also checked in various groups with positive (+) and negative (-) amyloid beta (Aβ). Ng highest levels of RoM were observed in the AD (<i>n</i> = 1894) compared to CTRL (<i>n</i> = 2051) group (RoM: 1.62). Similarly, the VILIP-1 highest values of RoM were detected in the AD (<i>n</i> = 706) compared to CTRL (<i>n</i> = 862) group (RoM: 1.34). Concentrations of both proteins increased in more advanced stages of AD. However, Ng seems to be an earlier biomarker for the assessment of cognitive impairment. Ng appears to be related with amyloid beta, and the highest levels of Ng in CSF was observed in the group with pathological Aβ+ status. Our meta-analysis confirms that Ng and VILIP-1 can be useful CSF biomarkers in differential diagnosis and monitoring progression of cognitive decline. Although, an additional advantage of the protein concentration Ng is the possibility of using it to predict the risk of developing cognitive impairment in normal controls with pathological levels of Aβ1-42. Analyses in larger cohorts are needed, particularly concerning Aβ status.https://www.mdpi.com/1422-0067/21/21/8335Alzheimer’s diseasemeta-analysissystematic reviewneurograninvisinin-like-protein-1
spellingShingle Maciej Dulewicz
Agnieszka Kulczyńska-Przybik
Barbara Mroczko
Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis
International Journal of Molecular Sciences
Alzheimer’s disease
meta-analysis
systematic review
neurogranin
visinin-like-protein-1
title Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis
title_full Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis
title_fullStr Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis
title_full_unstemmed Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis
title_short Neurogranin and VILIP-1 as Molecular Indicators of Neurodegeneration in Alzheimer’s Disease: A Systematic Review and Meta-Analysis
title_sort neurogranin and vilip 1 as molecular indicators of neurodegeneration in alzheimer s disease a systematic review and meta analysis
topic Alzheimer’s disease
meta-analysis
systematic review
neurogranin
visinin-like-protein-1
url https://www.mdpi.com/1422-0067/21/21/8335
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AT agnieszkakulczynskaprzybik neurograninandvilip1asmolecularindicatorsofneurodegenerationinalzheimersdiseaseasystematicreviewandmetaanalysis
AT barbaramroczko neurograninandvilip1asmolecularindicatorsofneurodegenerationinalzheimersdiseaseasystematicreviewandmetaanalysis