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Molecular pathology of age-related macular degeneration
Age-related macular degeneration (AMD) is a leading cause of irreversible blindness in the world. Although the etiology and pathogenesis of AMD remain largely unclear, a complex interaction of genetic and environmental factors is thought to exist. AMD pathology is characterized by degeneration invol...
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Published in: | Progress in retinal and eye research 2009-01, Vol.28 (1), p.1-18 |
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description | Age-related macular degeneration (AMD) is a leading cause of irreversible blindness in the world. Although the etiology and pathogenesis of AMD remain largely unclear, a complex interaction of genetic and environmental factors is thought to exist. AMD pathology is characterized by degeneration involving the retinal photoreceptors, retinal pigment epithelium, and Bruch's membrane, as well as, in some cases, alterations in choroidal capillaries. Recent research on the genetic and molecular underpinnings of AMD brings to light several basic molecular pathways and pathophysiological processes that might mediate AMD risk, progression, and/or response to therapy. This review summarizes, in detail, the molecular pathological findings in both humans and animal models, including genetic variations in
CFH, CX3CR1, and
ARMS2/HtrA1, as well as the role of numerous molecules implicated in inflammation, apoptosis, cholesterol trafficking, angiogenesis, and oxidative stress. |
doi_str_mv | 10.1016/j.preteyeres.2008.10.001 |
format | article |
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CFH, CX3CR1, and
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CFH, CX3CR1, and
ARMS2/HtrA1, as well as the role of numerous molecules implicated in inflammation, apoptosis, cholesterol trafficking, angiogenesis, and oxidative stress.</description><subject>Age-related macular degeneration</subject><subject>Animals</subject><subject>Bruch's membrane</subject><subject>Disease Models, Animal</subject><subject>Drusen</subject><subject>Genetics</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Macular Degeneration - genetics</subject><subject>Macular Degeneration - pathology</subject><subject>Molecular pathology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Retina - pathology</subject><subject>Retinal photoreceptors</subject><subject>Retinal pigment epithelium</subject><subject>Single nucleotide polymorphism</subject><subject>Vascular endothelial growth factor</subject><issn>1350-9462</issn><issn>1873-1635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkUFvGyEQhVGUKHHc_IVoT81pXYZdYPdSqY2atJKjXNIzmoWxjbVeXFhH8r8vlq2kvbQnEPPNe8M8xgrgM-CgPq1n20gj7SlSmgnOm_w84xzO2AQaXZWgKnme75XkZVsrccWuU1pzzhVv5SW7gpYLpRVMmH4KPdldj7HY4rgKfVjui7AocEllpB5HcsUGj4CjJQ0UcfRh-MAuFtgnujmdU_bz4dvL_fdy_vz44_7LvLRSy7HUUkrR2K7rUBJYrVFUNRe6wjyKsl0N6Cy4DjVgU_EadaMVglM1tJVDXU3Z56PudtdtyFkaxoi92Ua_wbg3Ab35uzL4lVmGVyM0ZOc6C9ydBGL4taM0mo1PlvoeBwq7ZJpsm9ehRCY__pNUqpVKCshgcwRtDClFWryNA9wc8jFr856POeRzqOR8cuvtn995bzwFkoGvR4DyUl89RZOsp8GS85HsaFzw_3f5DUNvp5Q</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Ding, Xiaoyan</creator><creator>Patel, Mrinali</creator><creator>Chan, Chi-Chao</creator><general>Elsevier Ltd</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>7X8</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20090101</creationdate><title>Molecular pathology of age-related macular degeneration</title><author>Ding, Xiaoyan ; Patel, Mrinali ; Chan, Chi-Chao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c575t-755528cbbba5e1c77a2340273a0606cb41adc1dba71a8304a7876a1d64193da73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Age-related macular degeneration</topic><topic>Animals</topic><topic>Bruch's membrane</topic><topic>Disease Models, Animal</topic><topic>Drusen</topic><topic>Genetics</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Macular Degeneration - genetics</topic><topic>Macular Degeneration - pathology</topic><topic>Molecular pathology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Retina - pathology</topic><topic>Retinal photoreceptors</topic><topic>Retinal pigment epithelium</topic><topic>Single nucleotide polymorphism</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Xiaoyan</creatorcontrib><creatorcontrib>Patel, Mrinali</creatorcontrib><creatorcontrib>Chan, Chi-Chao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Progress in retinal and eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Xiaoyan</au><au>Patel, Mrinali</au><au>Chan, Chi-Chao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular pathology of age-related macular degeneration</atitle><jtitle>Progress in retinal and eye research</jtitle><addtitle>Prog Retin Eye Res</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>28</volume><issue>1</issue><spage>1</spage><epage>18</epage><pages>1-18</pages><issn>1350-9462</issn><eissn>1873-1635</eissn><abstract>Age-related macular degeneration (AMD) is a leading cause of irreversible blindness in the world. Although the etiology and pathogenesis of AMD remain largely unclear, a complex interaction of genetic and environmental factors is thought to exist. AMD pathology is characterized by degeneration involving the retinal photoreceptors, retinal pigment epithelium, and Bruch's membrane, as well as, in some cases, alterations in choroidal capillaries. Recent research on the genetic and molecular underpinnings of AMD brings to light several basic molecular pathways and pathophysiological processes that might mediate AMD risk, progression, and/or response to therapy. This review summarizes, in detail, the molecular pathological findings in both humans and animal models, including genetic variations in
CFH, CX3CR1, and
ARMS2/HtrA1, as well as the role of numerous molecules implicated in inflammation, apoptosis, cholesterol trafficking, angiogenesis, and oxidative stress.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>19026761</pmid><doi>10.1016/j.preteyeres.2008.10.001</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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source | ScienceDirect Journals |
subjects | Age-related macular degeneration Animals Bruch's membrane Disease Models, Animal Drusen Genetics Humans Inflammation Macular Degeneration - genetics Macular Degeneration - pathology Molecular pathology Polymorphism, Single Nucleotide Retina - pathology Retinal photoreceptors Retinal pigment epithelium Single nucleotide polymorphism Vascular endothelial growth factor |
title | Molecular pathology of age-related macular degeneration |
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