Chitinase expression in Alzheimer's disease and non-demented brains regions
Abstract
Background Alzheimer disease is the most typical form of dementia. The causes of AD are not yet completely understood, but they include a combination of genetic, environmental and lifestyle factors that influence ja person's risk for developing the disease. New biomarkers related to these processes could be important for the diagnosis and follow-up of AD patients. Objective The intent of this study was to weigh the expression levels of chitinases genes in brain regions of late-onset AD (LOAD) patients. Materials and methods We analysed three microarray datasets obtained from the NCBI in order to verify the expression levels of chitinase genes family in brain biopsies (CR, DLPFC and VC) of LOAD patients compared to healthy subjects. We also divided the sample in function of sex difference and ages. Results The analysis showed that all chitinases genes were modulated in LOAD brain regions compared to healthy subjects. Furthermore positively correlation was identified between chitinases gene expression and healthy age's subjects. Moreover, it has been shown that CHI3L1 and CHI3L2 were regulated differently in healthy and LOAD brain depending on the sex. Conclusion It is possible to conclude that all chitinases could be considered new potential markers for LOAD disease.
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CHI3L2 may contribute to AD pathogenesis through neuroinflammatory processes.
“The eRNA ENSR00000011444 putatively regulates Chitinase-3-like protein 2 (CHI3L2), whose expression notably increases in the brains of patients with AD and may contribute to AD pathogenesis through neuroinflammatory processes (Fig. 3D) (50, 51).”
From Comprehensive characterization of the transcriptional landscape in Alzheimer’s disease (AD) brains (2025) · cites this paper as [51]
CHI3L2 expression notably increases in the brains of patients with AD.
“The eRNA ENSR00000011444 putatively regulates Chitinase-3-like protein 2 (CHI3L2), whose expression notably increases in the brains of patients with AD and may contribute to AD pathogenesis through neuroinflammatory processes (Fig. 3D) (50, 51).”
From Comprehensive characterization of the transcriptional landscape in Alzheimer’s disease (AD) brains (2025) · cites this paper as [51]
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References 62 · Cited by 54
- Authors
- Sanfilippo, C., Malaguarnera, L., & Di Rosa, M.
- Affiliations
- University of Catania (IT)
- Venue
- Journal of the Neurological Sciences
- Publisher
- Elsevier BV
- Published
- 2016-10
- Volume
- 369
- Pages
- 242-249
- ISSN
- 0022-510X (ISSN-L)
- OpenAlex
- W2516406792
- Cited by
- 54
- References
- 62
- Citations by year
- 2026: 1 · 2025: 9 · 2024: 4 · 2023: 5 · 2022: 14 · 2021: 5 · 2020: 8 · 2019: 3 · 2018: 2 · 2017: 2 · 2016: 1
- FWCI
- 2.14
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the Neurological Sciences (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Studies on Chitinases and Chitosanases
- Keywords
- chitinase, Alzheimer's disease, late-onset Alzheimer's disease, gene expression, YKL-40, CHI3L2, biomarkers, brain regions, dorsolateral prefrontal cortex, visual cortex, corpus callosum, sex differences, age
- MeSH terms
- Aged, Aged, 80 and over, Alzheimer Disease, Brain, Chitinases, Female, Gene Expression Regulation, Humans, Male, Sex Characteristics, Statistics, Nonparametric, Microarray Analysis
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