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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of molecular sciences 2020-10, Vol.21 (19), p.7290
Hauptverfasser: Ashok, Ajay, Singh, Neena, Chaudhary, Suman, Bellamkonda, Vindhya, Kritikos, Alexander E, Wise, Aaron S, Rana, Neil, McDonald, Dallas, Ayyagari, Rithvik
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 19
container_start_page 7290
container_title International journal of molecular sciences
container_volume 21
creator Ashok, Ajay
Singh, Neena
Chaudhary, Suman
Bellamkonda, Vindhya
Kritikos, Alexander E
Wise, Aaron S
Rana, Neil
McDonald, Dallas
Ayyagari, Rithvik
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
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7582766</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2449179611</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-b463237df97bc75ade9ee0cd0f01b8654c56e253122231cd88c481e2019880b33</originalsourceid><addsrcrecordid>eNpdkUtLxDAUhYMovneupeBCF1bzapO4GBgcXzAgiK5Dmt6OGdtUk86A_no7jA6jq3vgfhzOvQehI4IvGFP40k2bSAlRgiq8gXYJpzTFOBeba3oH7cU4xZgymqlttMNYL4mSu2jwBJ3zpk5GMAEPwXSu9YnxZTKsv17BNRBOYzJyEUyEq2Tok5t5W8-dnyRj598O0FZl6giHP3MfvdzePF_fp-PHu4fr4Ti1XMguLXjOKBNlpURhRWZKUADYlrjCpJB5xm2WA80YobTPZUspLZcEKO4zSlwwto8GS9_3WdFAacF3wdT6PbjGhE_dGqf_brx71ZN2rkUmqcjz3uDsxyC0HzOInW5ctFDXxkM7i5pyrohQOSE9evIPnbaz0P-opzIuc0E4WRieLykb2hgDVKswBOtFMXq9mB4_Xj9gBf82wb4BTAaH4g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2548671416</pqid></control><display><type>article</type><title>Retinal Degeneration and Alzheimer's Disease: An Evolving Link</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Ashok, Ajay ; Singh, Neena ; Chaudhary, Suman ; Bellamkonda, Vindhya ; Kritikos, Alexander E ; Wise, Aaron S ; Rana, Neil ; McDonald, Dallas ; Ayyagari, Rithvik</creator><creatorcontrib>Ashok, Ajay ; Singh, Neena ; Chaudhary, Suman ; Bellamkonda, Vindhya ; Kritikos, Alexander E ; Wise, Aaron S ; Rana, Neil ; McDonald, Dallas ; Ayyagari, Rithvik</creatorcontrib><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><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 - genetics</subject><subject>tau Proteins - metabolism</subject><subject>Toxicity</subject><subject>Visual cortex</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkUtLxDAUhYMovneupeBCF1bzapO4GBgcXzAgiK5Dmt6OGdtUk86A_no7jA6jq3vgfhzOvQehI4IvGFP40k2bSAlRgiq8gXYJpzTFOBeba3oH7cU4xZgymqlttMNYL4mSu2jwBJ3zpk5GMAEPwXSu9YnxZTKsv17BNRBOYzJyEUyEq2Tok5t5W8-dnyRj598O0FZl6giHP3MfvdzePF_fp-PHu4fr4Ti1XMguLXjOKBNlpURhRWZKUADYlrjCpJB5xm2WA80YobTPZUspLZcEKO4zSlwwto8GS9_3WdFAacF3wdT6PbjGhE_dGqf_brx71ZN2rkUmqcjz3uDsxyC0HzOInW5ctFDXxkM7i5pyrohQOSE9evIPnbaz0P-opzIuc0E4WRieLykb2hgDVKswBOtFMXq9mB4_Xj9gBf82wb4BTAaH4g</recordid><startdate>20201002</startdate><enddate>20201002</enddate><creator>Ashok, Ajay</creator><creator>Singh, Neena</creator><creator>Chaudhary, Suman</creator><creator>Bellamkonda, Vindhya</creator><creator>Kritikos, Alexander E</creator><creator>Wise, Aaron S</creator><creator>Rana, Neil</creator><creator>McDonald, Dallas</creator><creator>Ayyagari, Rithvik</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><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></search><sort><creationdate>20201002</creationdate><title>Retinal Degeneration and Alzheimer's Disease: An Evolving Link</title><author>Ashok, Ajay ; Singh, Neena ; Chaudhary, Suman ; Bellamkonda, Vindhya ; Kritikos, Alexander E ; Wise, Aaron S ; Rana, Neil ; McDonald, Dallas ; Ayyagari, Rithvik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-b463237df97bc75ade9ee0cd0f01b8654c56e253122231cd88c481e2019880b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Abnormalities</topic><topic>Accumulation</topic><topic>Alzheimer Disease - complications</topic><topic>Alzheimer Disease - genetics</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's disease</topic><topic>Amyloid</topic><topic>Amyloid beta-Peptides - genetics</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Animal cognition</topic><topic>Biomarkers</topic><topic>Blindness</topic><topic>Brain</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Chelation</topic><topic>Dementia disorders</topic><topic>Glaucoma</topic><topic>Glaucoma - complications</topic><topic>Glaucoma - genetics</topic><topic>Glaucoma - pathology</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Iron</topic><topic>Macular degeneration</topic><topic>Macular Degeneration - complications</topic><topic>Macular Degeneration - genetics</topic><topic>Macular Degeneration - pathology</topic><topic>Neurodegeneration</topic><topic>Neuroprotection</topic><topic>Oxidative stress</topic><topic>Pathology</topic><topic>Phosphorylation</topic><topic>Photoreceptors</topic><topic>Prion protein</topic><topic>Protein Aggregation, Pathological - genetics</topic><topic>Protein Aggregation, Pathological - pathology</topic><topic>Proteins</topic><topic>Retina</topic><topic>Retina - metabolism</topic><topic>Retina - pathology</topic><topic>Retinal cells</topic><topic>Retinal degeneration</topic><topic>Retinal Degeneration - genetics</topic><topic>Retinal Degeneration - metabolism</topic><topic>Retinal Degeneration - pathology</topic><topic>Retinal ganglion cells</topic><topic>Retinal Ganglion Cells - metabolism</topic><topic>Retinal Ganglion Cells - pathology</topic><topic>Review</topic><topic>Tau protein</topic><topic>tau Proteins - genetics</topic><topic>tau Proteins - metabolism</topic><topic>Toxicity</topic><topic>Visual cortex</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ashok, Ajay</au><au>Singh, Neena</au><au>Chaudhary, Suman</au><au>Bellamkonda, Vindhya</au><au>Kritikos, Alexander E</au><au>Wise, Aaron S</au><au>Rana, Neil</au><au>McDonald, Dallas</au><au>Ayyagari, Rithvik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinal Degeneration and Alzheimer's Disease: An Evolving Link</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2020-10-02</date><risdate>2020</risdate><volume>21</volume><issue>19</issue><spage>7290</spage><pages>7290-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>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.</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>
fulltext fulltext
identifier ISSN: 1422-0067
ispartof International journal of molecular sciences, 2020-10, Vol.21 (19), p.7290
issn 1422-0067
1661-6596
1422-0067
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7582766
source MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T01%3A15%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Retinal%20Degeneration%20and%20Alzheimer's%20Disease:%20An%20Evolving%20Link&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Ashok,%20Ajay&rft.date=2020-10-02&rft.volume=21&rft.issue=19&rft.spage=7290&rft.pages=7290-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms21197290&rft_dat=%3Cproquest_pubme%3E2449179611%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2548671416&rft_id=info:pmid/33023198&rfr_iscdi=true