LOC387715/HTRA1 and Complement Factor H Variants in Patients with Age-Related Macular Degeneration Seen at the Mayo Clinic
Purpose: To confirm association of the complement factor H allelic variant (CFH Y402H) and the LOC387715/HTRA1 (LOC387715 A69S) risk alleles with age-related macular degeneration (AMD). Study Population: Study of 89 Caucasian patients with neovascular (exudative) AMD and 232 Caucasian controls.Metho...
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Veröffentlicht in: | Ophthalmic genetics 2007-12, Vol.28 (4), p.203-207 |
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creator | Pulido, Jose S. Peterson, Lisa M. Mutapcic, Lejla Bryant, Sandra Highsmith, W. Edward |
description | Purpose: To confirm association of the complement factor H allelic variant (CFH Y402H) and the LOC387715/HTRA1 (LOC387715 A69S) risk alleles with age-related macular degeneration (AMD). Study Population: Study of 89 Caucasian patients with neovascular (exudative) AMD and 232 Caucasian controls.Methods: The Y402H variant of CFH gene and A69S variant of LOC387715/HTRA1 gene locus were examined.Results: For CFH, the odds ratio for the homozygous variant was 4.97 (CI 2.52 to 9.79). For LOC387715/HTRA1 the odds ratio for the homozygous risk variant was 7.75 (CI 3.46 to 17.35). The odds ratio for heterozygous carriers was 3.35 (CI 1.91 to 5.90). |
doi_str_mv | 10.1080/13816810701649617 |
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Edward</creator><creatorcontrib>Pulido, Jose S. ; Peterson, Lisa M. ; Mutapcic, Lejla ; Bryant, Sandra ; Highsmith, W. Edward</creatorcontrib><description>Purpose: To confirm association of the complement factor H allelic variant (CFH Y402H) and the LOC387715/HTRA1 (LOC387715 A69S) risk alleles with age-related macular degeneration (AMD). Study Population: Study of 89 Caucasian patients with neovascular (exudative) AMD and 232 Caucasian controls.Methods: The Y402H variant of CFH gene and A69S variant of LOC387715/HTRA1 gene locus were examined.Results: For CFH, the odds ratio for the homozygous variant was 4.97 (CI 2.52 to 9.79). For LOC387715/HTRA1 the odds ratio for the homozygous risk variant was 7.75 (CI 3.46 to 17.35). The odds ratio for heterozygous carriers was 3.35 (CI 1.91 to 5.90).</description><identifier>ISSN: 1381-6810</identifier><identifier>EISSN: 1744-5094</identifier><identifier>DOI: 10.1080/13816810701649617</identifier><identifier>PMID: 18161619</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Age-related macular degeneration ; association study ; Base Sequence ; Complement Factor H - genetics ; complement H ; DNA Primers ; Genetic Predisposition to Disease ; genetics ; Humans ; Macular Degeneration - genetics ; Minnesota ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide</subject><ispartof>Ophthalmic genetics, 2007-12, Vol.28 (4), p.203-207</ispartof><rights>2007 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-d31c4d7e5947c9fa4d707ef0b7cbe419e4007f093f12c65e7d453e25ffa036d13</citedby><cites>FETCH-LOGICAL-c435t-d31c4d7e5947c9fa4d707ef0b7cbe419e4007f093f12c65e7d453e25ffa036d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/13816810701649617$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/13816810701649617$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,59626,59732,60415,60521,61200,61235,61381,61416</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18161619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pulido, Jose S.</creatorcontrib><creatorcontrib>Peterson, Lisa M.</creatorcontrib><creatorcontrib>Mutapcic, Lejla</creatorcontrib><creatorcontrib>Bryant, Sandra</creatorcontrib><creatorcontrib>Highsmith, W. Edward</creatorcontrib><title>LOC387715/HTRA1 and Complement Factor H Variants in Patients with Age-Related Macular Degeneration Seen at the Mayo Clinic</title><title>Ophthalmic genetics</title><addtitle>Ophthalmic Genet</addtitle><description>Purpose: To confirm association of the complement factor H allelic variant (CFH Y402H) and the LOC387715/HTRA1 (LOC387715 A69S) risk alleles with age-related macular degeneration (AMD). Study Population: Study of 89 Caucasian patients with neovascular (exudative) AMD and 232 Caucasian controls.Methods: The Y402H variant of CFH gene and A69S variant of LOC387715/HTRA1 gene locus were examined.Results: For CFH, the odds ratio for the homozygous variant was 4.97 (CI 2.52 to 9.79). For LOC387715/HTRA1 the odds ratio for the homozygous risk variant was 7.75 (CI 3.46 to 17.35). The odds ratio for heterozygous carriers was 3.35 (CI 1.91 to 5.90).</description><subject>Age-related macular degeneration</subject><subject>association study</subject><subject>Base Sequence</subject><subject>Complement Factor H - genetics</subject><subject>complement H</subject><subject>DNA Primers</subject><subject>Genetic Predisposition to Disease</subject><subject>genetics</subject><subject>Humans</subject><subject>Macular Degeneration - genetics</subject><subject>Minnesota</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Single Nucleotide</subject><issn>1381-6810</issn><issn>1744-5094</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV-L1DAUxYso7h_9AL5Innyrm9ukTYu-DNV1hJGVdfW1ZNKbnSxpMpukLOOn3wwzICKs3Id7IL9zuOQUxRug74G29AJYC00LVFBoeNeAeFacguC8rGnHn2ed38s9cFKcxXhHaVUB1C-LE8i-PN1p8Xt11bNWCKgvljfXCyDSjaT309bihC6RS6mSD2RJfslgpEuRGEe-y2Rwrx9M2pDFLZbXaGXCkXyTarYykE94iw5D5rwjPxAdkYmkDWZg50lvjTPqVfFCSxvx9XGfFz8vP9_0y3J19eVrv1iVirM6lSMDxUeBdceF6rTMmgrUdC3UGjl0yCkVmnZMQ6WaGsXIa4ZVrbWkrBmBnRfvDrnb4O9njGmYTFRorXTo5zg0HW0Z4-1_wYoCF11bZxAOoAo-xoB62AYzybAbgA77ZoZ_msmet8fweT3h-MdxrCIDHw-AcdqHST74YMchyZ31QQfplIkDeyr_w1_2DUqbNkoGHO78HFz-4SeuewSXRqwL</recordid><startdate>20071201</startdate><enddate>20071201</enddate><creator>Pulido, Jose S.</creator><creator>Peterson, Lisa M.</creator><creator>Mutapcic, Lejla</creator><creator>Bryant, Sandra</creator><creator>Highsmith, W. Edward</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20071201</creationdate><title>LOC387715/HTRA1 and Complement Factor H Variants in Patients with Age-Related Macular Degeneration Seen at the Mayo Clinic</title><author>Pulido, Jose S. ; Peterson, Lisa M. ; Mutapcic, Lejla ; Bryant, Sandra ; Highsmith, W. Edward</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-d31c4d7e5947c9fa4d707ef0b7cbe419e4007f093f12c65e7d453e25ffa036d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Age-related macular degeneration</topic><topic>association study</topic><topic>Base Sequence</topic><topic>Complement Factor H - genetics</topic><topic>complement H</topic><topic>DNA Primers</topic><topic>Genetic Predisposition to Disease</topic><topic>genetics</topic><topic>Humans</topic><topic>Macular Degeneration - genetics</topic><topic>Minnesota</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Single Nucleotide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pulido, Jose S.</creatorcontrib><creatorcontrib>Peterson, Lisa M.</creatorcontrib><creatorcontrib>Mutapcic, Lejla</creatorcontrib><creatorcontrib>Bryant, Sandra</creatorcontrib><creatorcontrib>Highsmith, W. Edward</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Ophthalmic genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pulido, Jose S.</au><au>Peterson, Lisa M.</au><au>Mutapcic, Lejla</au><au>Bryant, Sandra</au><au>Highsmith, W. Edward</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LOC387715/HTRA1 and Complement Factor H Variants in Patients with Age-Related Macular Degeneration Seen at the Mayo Clinic</atitle><jtitle>Ophthalmic genetics</jtitle><addtitle>Ophthalmic Genet</addtitle><date>2007-12-01</date><risdate>2007</risdate><volume>28</volume><issue>4</issue><spage>203</spage><epage>207</epage><pages>203-207</pages><issn>1381-6810</issn><eissn>1744-5094</eissn><abstract>Purpose: To confirm association of the complement factor H allelic variant (CFH Y402H) and the LOC387715/HTRA1 (LOC387715 A69S) risk alleles with age-related macular degeneration (AMD). Study Population: Study of 89 Caucasian patients with neovascular (exudative) AMD and 232 Caucasian controls.Methods: The Y402H variant of CFH gene and A69S variant of LOC387715/HTRA1 gene locus were examined.Results: For CFH, the odds ratio for the homozygous variant was 4.97 (CI 2.52 to 9.79). For LOC387715/HTRA1 the odds ratio for the homozygous risk variant was 7.75 (CI 3.46 to 17.35). The odds ratio for heterozygous carriers was 3.35 (CI 1.91 to 5.90).</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>18161619</pmid><doi>10.1080/13816810701649617</doi><tpages>5</tpages></addata></record> |
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subjects | Age-related macular degeneration association study Base Sequence Complement Factor H - genetics complement H DNA Primers Genetic Predisposition to Disease genetics Humans Macular Degeneration - genetics Minnesota Polymerase Chain Reaction Polymorphism, Single Nucleotide |
title | LOC387715/HTRA1 and Complement Factor H Variants in Patients with Age-Related Macular Degeneration Seen at the Mayo Clinic |
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