Retinal Degeneration and Alzheimer's Disease: An Evolving Link
Age-related macular degeneration (AMD) and glaucoma are degenerative conditions of the retina and a significant cause of irreversible blindness in developed countries. Alzheimer's disease (AD), the most common dementia of the elderly, is often associated with AMD and glaucoma. The cardinal feat...
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Veröffentlicht in: | International journal of molecular sciences 2020-10, Vol.21 (19), p.7290 |
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description | Age-related macular degeneration (AMD) and glaucoma are degenerative conditions of the retina and a significant cause of irreversible blindness in developed countries. Alzheimer's disease (AD), the most common dementia of the elderly, is often associated with AMD and glaucoma. The cardinal features of AD include extracellular accumulation of amyloid β (Aβ) and intracellular deposits of hyper-phosphorylated tau (p-tau). Neuroinflammation and brain iron dyshomeostasis accompany Aβ and p-tau deposits and, together, lead to progressive neuronal death and dementia. The accumulation of Aβ and iron in drusen, the hallmark of AMD, and Aβ and p-tau in retinal ganglion cells (RGC), the main retinal cell type implicated in glaucoma, and accompanying inflammation suggest overlapping pathology. Visual abnormalities are prominent in AD and are believed to develop before cognitive decline. Some are caused by degeneration of the visual cortex, while others are due to RGC loss or AMD-associated retinal degeneration. Here, we review recent information on Aβ, p-tau, chronic inflammation, and iron dyshomeostasis as common pathogenic mechanisms linking the three degenerative conditions, and iron chelation as a common therapeutic option for these disorders. Additionally discussed is the role of prion protein, infamous for prion disorders, in Aβ-mediated toxicity and, paradoxically, in neuroprotection. |
doi_str_mv | 10.3390/ijms21197290 |
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Alzheimer's disease (AD), the most common dementia of the elderly, is often associated with AMD and glaucoma. The cardinal features of AD include extracellular accumulation of amyloid β (Aβ) and intracellular deposits of hyper-phosphorylated tau (p-tau). Neuroinflammation and brain iron dyshomeostasis accompany Aβ and p-tau deposits and, together, lead to progressive neuronal death and dementia. The accumulation of Aβ and iron in drusen, the hallmark of AMD, and Aβ and p-tau in retinal ganglion cells (RGC), the main retinal cell type implicated in glaucoma, and accompanying inflammation suggest overlapping pathology. Visual abnormalities are prominent in AD and are believed to develop before cognitive decline. Some are caused by degeneration of the visual cortex, while others are due to RGC loss or AMD-associated retinal degeneration. Here, we review recent information on Aβ, p-tau, chronic inflammation, and iron dyshomeostasis as common pathogenic mechanisms linking the three degenerative conditions, and iron chelation as a common therapeutic option for these disorders. Additionally discussed is the role of prion protein, infamous for prion disorders, in Aβ-mediated toxicity and, paradoxically, in neuroprotection.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21197290</identifier><identifier>PMID: 33023198</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abnormalities ; Accumulation ; Alzheimer Disease - complications ; Alzheimer Disease - genetics ; Alzheimer Disease - pathology ; Alzheimer's disease ; Amyloid ; Amyloid beta-Peptides - genetics ; Amyloid beta-Peptides - metabolism ; Animal cognition ; Biomarkers ; Blindness ; Brain ; Brain - metabolism ; Brain - pathology ; Chelation ; Dementia disorders ; Glaucoma ; Glaucoma - complications ; Glaucoma - genetics ; Glaucoma - pathology ; Humans ; Inflammation ; Iron ; Macular degeneration ; Macular Degeneration - complications ; Macular Degeneration - genetics ; Macular Degeneration - pathology ; Neurodegeneration ; Neuroprotection ; Oxidative stress ; Pathology ; Phosphorylation ; Photoreceptors ; Prion protein ; Protein Aggregation, Pathological - genetics ; Protein Aggregation, Pathological - pathology ; Proteins ; Retina ; Retina - metabolism ; Retina - pathology ; Retinal cells ; Retinal degeneration ; Retinal Degeneration - genetics ; Retinal Degeneration - metabolism ; Retinal Degeneration - pathology ; Retinal ganglion cells ; Retinal Ganglion Cells - metabolism ; Retinal Ganglion Cells - pathology ; Review ; Tau protein ; tau Proteins - genetics ; tau Proteins - metabolism ; Toxicity ; Visual cortex</subject><ispartof>International journal of molecular sciences, 2020-10, Vol.21 (19), p.7290</ispartof><rights>2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-b463237df97bc75ade9ee0cd0f01b8654c56e253122231cd88c481e2019880b33</citedby><cites>FETCH-LOGICAL-c478t-b463237df97bc75ade9ee0cd0f01b8654c56e253122231cd88c481e2019880b33</cites><orcidid>0000-0001-8369-7517 ; 0000-0003-4354-1467 ; 0000-0002-4035-2241</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582766/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582766/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33023198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ashok, Ajay</creatorcontrib><creatorcontrib>Singh, Neena</creatorcontrib><creatorcontrib>Chaudhary, Suman</creatorcontrib><creatorcontrib>Bellamkonda, Vindhya</creatorcontrib><creatorcontrib>Kritikos, Alexander E</creatorcontrib><creatorcontrib>Wise, Aaron S</creatorcontrib><creatorcontrib>Rana, Neil</creatorcontrib><creatorcontrib>McDonald, Dallas</creatorcontrib><creatorcontrib>Ayyagari, Rithvik</creatorcontrib><title>Retinal Degeneration and Alzheimer's Disease: An Evolving Link</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Age-related macular degeneration (AMD) and glaucoma are degenerative conditions of the retina and a significant cause of irreversible blindness in developed countries. Alzheimer's disease (AD), the most common dementia of the elderly, is often associated with AMD and glaucoma. The cardinal features of AD include extracellular accumulation of amyloid β (Aβ) and intracellular deposits of hyper-phosphorylated tau (p-tau). Neuroinflammation and brain iron dyshomeostasis accompany Aβ and p-tau deposits and, together, lead to progressive neuronal death and dementia. The accumulation of Aβ and iron in drusen, the hallmark of AMD, and Aβ and p-tau in retinal ganglion cells (RGC), the main retinal cell type implicated in glaucoma, and accompanying inflammation suggest overlapping pathology. Visual abnormalities are prominent in AD and are believed to develop before cognitive decline. Some are caused by degeneration of the visual cortex, while others are due to RGC loss or AMD-associated retinal degeneration. Here, we review recent information on Aβ, p-tau, chronic inflammation, and iron dyshomeostasis as common pathogenic mechanisms linking the three degenerative conditions, and iron chelation as a common therapeutic option for these disorders. Additionally discussed is the role of prion protein, infamous for prion disorders, in Aβ-mediated toxicity and, paradoxically, in neuroprotection.</description><subject>Abnormalities</subject><subject>Accumulation</subject><subject>Alzheimer Disease - complications</subject><subject>Alzheimer Disease - genetics</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Amyloid</subject><subject>Amyloid beta-Peptides - genetics</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Animal cognition</subject><subject>Biomarkers</subject><subject>Blindness</subject><subject>Brain</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Chelation</subject><subject>Dementia disorders</subject><subject>Glaucoma</subject><subject>Glaucoma - complications</subject><subject>Glaucoma - genetics</subject><subject>Glaucoma - pathology</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Iron</subject><subject>Macular degeneration</subject><subject>Macular Degeneration - complications</subject><subject>Macular Degeneration - genetics</subject><subject>Macular Degeneration - pathology</subject><subject>Neurodegeneration</subject><subject>Neuroprotection</subject><subject>Oxidative stress</subject><subject>Pathology</subject><subject>Phosphorylation</subject><subject>Photoreceptors</subject><subject>Prion protein</subject><subject>Protein Aggregation, Pathological - genetics</subject><subject>Protein Aggregation, Pathological - pathology</subject><subject>Proteins</subject><subject>Retina</subject><subject>Retina - metabolism</subject><subject>Retina - pathology</subject><subject>Retinal cells</subject><subject>Retinal degeneration</subject><subject>Retinal Degeneration - genetics</subject><subject>Retinal Degeneration - metabolism</subject><subject>Retinal Degeneration - pathology</subject><subject>Retinal ganglion cells</subject><subject>Retinal Ganglion Cells - metabolism</subject><subject>Retinal Ganglion Cells - pathology</subject><subject>Review</subject><subject>Tau protein</subject><subject>tau Proteins - 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Alzheimer's disease (AD), the most common dementia of the elderly, is often associated with AMD and glaucoma. The cardinal features of AD include extracellular accumulation of amyloid β (Aβ) and intracellular deposits of hyper-phosphorylated tau (p-tau). Neuroinflammation and brain iron dyshomeostasis accompany Aβ and p-tau deposits and, together, lead to progressive neuronal death and dementia. The accumulation of Aβ and iron in drusen, the hallmark of AMD, and Aβ and p-tau in retinal ganglion cells (RGC), the main retinal cell type implicated in glaucoma, and accompanying inflammation suggest overlapping pathology. Visual abnormalities are prominent in AD and are believed to develop before cognitive decline. Some are caused by degeneration of the visual cortex, while others are due to RGC loss or AMD-associated retinal degeneration. Here, we review recent information on Aβ, p-tau, chronic inflammation, and iron dyshomeostasis as common pathogenic mechanisms linking the three degenerative conditions, and iron chelation as a common therapeutic option for these disorders. Additionally discussed is the role of prion protein, infamous for prion disorders, in Aβ-mediated toxicity and, paradoxically, in neuroprotection.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>33023198</pmid><doi>10.3390/ijms21197290</doi><orcidid>https://orcid.org/0000-0001-8369-7517</orcidid><orcidid>https://orcid.org/0000-0003-4354-1467</orcidid><orcidid>https://orcid.org/0000-0002-4035-2241</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abnormalities Accumulation Alzheimer Disease - complications Alzheimer Disease - genetics Alzheimer Disease - pathology Alzheimer's disease Amyloid Amyloid beta-Peptides - genetics Amyloid beta-Peptides - metabolism Animal cognition Biomarkers Blindness Brain Brain - metabolism Brain - pathology Chelation Dementia disorders Glaucoma Glaucoma - complications Glaucoma - genetics Glaucoma - pathology Humans Inflammation Iron Macular degeneration Macular Degeneration - complications Macular Degeneration - genetics Macular Degeneration - pathology Neurodegeneration Neuroprotection Oxidative stress Pathology Phosphorylation Photoreceptors Prion protein Protein Aggregation, Pathological - genetics Protein Aggregation, Pathological - pathology Proteins Retina Retina - metabolism Retina - pathology Retinal cells Retinal degeneration Retinal Degeneration - genetics Retinal Degeneration - metabolism Retinal Degeneration - pathology Retinal ganglion cells Retinal Ganglion Cells - metabolism Retinal Ganglion Cells - pathology Review Tau protein tau Proteins - genetics tau Proteins - metabolism Toxicity Visual cortex |
title | Retinal Degeneration and Alzheimer's Disease: An Evolving Link |
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