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Glia-Mediated Retinal Neuroinflammation as a Biomarker in Alzheimer's Disease
- Source :
- Ophthalmic research. 54(4)
- Publication Year :
- 2015
-
Abstract
- Alzheimer's disease (AD) is the most common type of dementia worldwide; it is characterized by a progressive decline in cognitive functions and memory, resulting from synaptic and cell loss, and accompanied by a strong neuroinflammatory response. Besides the vast progress in the understanding of the pathophysiology of AD in the past decades, there is still no effective treatment. Moreover, the diagnosis occurs usually at an advanced stage of the disease, where the neurological damage has already occurred. The identification of biomarkers that would allow an early diagnosis of this disease is a major goal that would also help managing AD progression. Due to its cellular and physiological resemblances with the brain, the retina has long been regarded as a window to the brain. Several brain manifestations have been associated with retinal alterations. In AD patients, some structural and functional alterations in the retina can be associated with disease onset. However, only a few studies have focused on the alterations in retinal glial cells associated with AD. This review aims at giving an overview of the AD-associated retinal alterations, particularly in glial cells. The documented alterations in retinal glia will be discussed concerning their potential to predict the brain alterations occurring in AD.
- Subjects :
- Pathology
medicine.medical_specialty
Biology
Cellular and Molecular Neuroscience
chemistry.chemical_compound
Alzheimer Disease
medicine
Dementia
Humans
Neuroinflammation
Retina
Neurodegeneration
Retinitis
Retinal
General Medicine
medicine.disease
Sensory Systems
Ophthalmology
medicine.anatomical_structure
Early Diagnosis
chemistry
Neuroglia
Biomarker (medicine)
Alzheimer's disease
Neuroscience
Biomarkers
Retinal Neurons
Subjects
Details
- ISSN :
- 14230259
- Volume :
- 54
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Ophthalmic research
- Accession number :
- edsair.doi.dedup.....4e149ee9c2035b5bc6c2d10d961b9819