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Promoter polymorphisms of the pigment epithelium-derived factor gene are associated with diabetic retinopathy
Pigment epithelium-derived factor (PEDF or SERPINF1), a neuroprotective and anti-angiogenic factor, may play an important role in the pathogenesis of diabetic retinopathy (DR). In 416 patients with type 2 diabetes, four polymorphisms in the PEDF SNPs were identified, rs12150053 and rs12948385 in the...
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Published in: | Biochemical and biophysical research communications 2007-09, Vol.361 (2), p.421-426 |
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container_title | Biochemical and biophysical research communications |
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creator | Iizuka, Hiroyuki Awata, Takuya Osaki, Masataka Neda, Tamotsu Kurihara, Susumu Inoue, Kiyoaki Inukai, Kouichi Kabasawa, Sho Mori, Keisuke Yoneya, Shin Katayama, Shigehiro |
description | Pigment epithelium-derived factor (PEDF or SERPINF1), a neuroprotective and anti-angiogenic factor, may play an important role in the pathogenesis of diabetic retinopathy (DR). In 416 patients with type 2 diabetes, four polymorphisms in the PEDF SNPs were identified, rs12150053 and rs12948385 in the promoter region, rs9913583 in the 5′-untranslated region, and rs1136287 (Met72Thr) in exon 3. Based on case-control studies, rs12150053 and rs12948385, but not rs9913583 and rs1136287, were significantly associated with DR. A logistic regression analysis revealed that the TC or CC genotype of rs12150053 was a significant risk factor for DR (odds ratio 2.40, p=0.0004). The GA or AA genotype of rs12948385 was also a significant risk factor for DR. In addition, a significant interaction between the vascular endothelial growth factor (VEGF) and PEDF SNPs in the susceptibility to DR was found. These results demonstrate that the PEDF gene, in cooperation with the VEGF gene, may contribute to the development of DR. |
doi_str_mv | 10.1016/j.bbrc.2007.07.025 |
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In 416 patients with type 2 diabetes, four polymorphisms in the PEDF SNPs were identified, rs12150053 and rs12948385 in the promoter region, rs9913583 in the 5′-untranslated region, and rs1136287 (Met72Thr) in exon 3. Based on case-control studies, rs12150053 and rs12948385, but not rs9913583 and rs1136287, were significantly associated with DR. A logistic regression analysis revealed that the TC or CC genotype of rs12150053 was a significant risk factor for DR (odds ratio 2.40, p=0.0004). The GA or AA genotype of rs12948385 was also a significant risk factor for DR. In addition, a significant interaction between the vascular endothelial growth factor (VEGF) and PEDF SNPs in the susceptibility to DR was found. These results demonstrate that the PEDF gene, in cooperation with the VEGF gene, may contribute to the development of DR.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2007.07.025</identifier><identifier>PMID: 17658465</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Case-Control Studies ; Diabetic macular edema ; Diabetic retinopathy ; Diabetic Retinopathy - genetics ; Eye Proteins - genetics ; Female ; Genetic Predisposition to Disease ; Haplotypes ; Humans ; Interaction ; Linkage Disequilibrium - genetics ; Logistic Models ; Male ; Middle Aged ; Nerve Growth Factors - genetics ; Pigment epithelium-derived factor gene ; Polymorphism, Single Nucleotide - genetics ; Promoter Regions, Genetic - genetics ; Serpins - genetics ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - genetics</subject><ispartof>Biochemical and biophysical research communications, 2007-09, Vol.361 (2), p.421-426</ispartof><rights>2007 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-4cb0ede6b04e5293e2020fe2454429dbc26e23d959ad31472d62293a2a8864893</citedby><cites>FETCH-LOGICAL-c385t-4cb0ede6b04e5293e2020fe2454429dbc26e23d959ad31472d62293a2a8864893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17658465$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iizuka, Hiroyuki</creatorcontrib><creatorcontrib>Awata, Takuya</creatorcontrib><creatorcontrib>Osaki, Masataka</creatorcontrib><creatorcontrib>Neda, Tamotsu</creatorcontrib><creatorcontrib>Kurihara, Susumu</creatorcontrib><creatorcontrib>Inoue, Kiyoaki</creatorcontrib><creatorcontrib>Inukai, Kouichi</creatorcontrib><creatorcontrib>Kabasawa, Sho</creatorcontrib><creatorcontrib>Mori, Keisuke</creatorcontrib><creatorcontrib>Yoneya, Shin</creatorcontrib><creatorcontrib>Katayama, Shigehiro</creatorcontrib><title>Promoter polymorphisms of the pigment epithelium-derived factor gene are associated with diabetic retinopathy</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Pigment epithelium-derived factor (PEDF or SERPINF1), a neuroprotective and anti-angiogenic factor, may play an important role in the pathogenesis of diabetic retinopathy (DR). In 416 patients with type 2 diabetes, four polymorphisms in the PEDF SNPs were identified, rs12150053 and rs12948385 in the promoter region, rs9913583 in the 5′-untranslated region, and rs1136287 (Met72Thr) in exon 3. Based on case-control studies, rs12150053 and rs12948385, but not rs9913583 and rs1136287, were significantly associated with DR. A logistic regression analysis revealed that the TC or CC genotype of rs12150053 was a significant risk factor for DR (odds ratio 2.40, p=0.0004). The GA or AA genotype of rs12948385 was also a significant risk factor for DR. In addition, a significant interaction between the vascular endothelial growth factor (VEGF) and PEDF SNPs in the susceptibility to DR was found. These results demonstrate that the PEDF gene, in cooperation with the VEGF gene, may contribute to the development of DR.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Case-Control Studies</subject><subject>Diabetic macular edema</subject><subject>Diabetic retinopathy</subject><subject>Diabetic Retinopathy - genetics</subject><subject>Eye Proteins - genetics</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Haplotypes</subject><subject>Humans</subject><subject>Interaction</subject><subject>Linkage Disequilibrium - genetics</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nerve Growth Factors - genetics</subject><subject>Pigment epithelium-derived factor gene</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Serpins - genetics</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - genetics</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkU1rGzEQhkVpaZykf6CHolNv60paSV5BLiGkbSDQHlrITWil2VhmtdpKsov_fbXYkFsK88Ewz7yHeRH6SMmaEiq_7NZ9n-yaEbJZL8HEG7SiRJGGUcLfohUhRDZM0acLdJnzjhBKuVTv0QXdSNFxKVYo_EwxxAIJz3E8hpjmrc8h4zjgsgU8--cAU8Ew-zqOfh8aB8kfwOHB2BITfoYJsEk1c47Wm1JXfyuMnTc9FG9xqnWKsynb4zV6N5gxw4dzv0K_v97_uvvePP749nB3-9jYthOl4bYn4ED2hINgqgVGGBmAccE5U663TAJrnRLKuJbyDXOSVcww03WSd6q9Qp9PunOKf_aQiw4-WxhHM0HcZy072komu_-CVG1aJegCshNoU8w5waDn5INJR02JXtzQO724oRc39BJM1KNPZ_V9H8C9nJzfX4GbEwD1GQcPSWfrYbLgfAJbtIv-Nf1_WZCc6g</recordid><startdate>20070921</startdate><enddate>20070921</enddate><creator>Iizuka, Hiroyuki</creator><creator>Awata, Takuya</creator><creator>Osaki, Masataka</creator><creator>Neda, Tamotsu</creator><creator>Kurihara, Susumu</creator><creator>Inoue, Kiyoaki</creator><creator>Inukai, Kouichi</creator><creator>Kabasawa, Sho</creator><creator>Mori, Keisuke</creator><creator>Yoneya, Shin</creator><creator>Katayama, Shigehiro</creator><general>Elsevier Inc</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>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070921</creationdate><title>Promoter polymorphisms of the pigment epithelium-derived factor gene are associated with diabetic retinopathy</title><author>Iizuka, Hiroyuki ; Awata, Takuya ; Osaki, Masataka ; Neda, Tamotsu ; Kurihara, Susumu ; Inoue, Kiyoaki ; Inukai, Kouichi ; Kabasawa, Sho ; Mori, Keisuke ; Yoneya, Shin ; Katayama, Shigehiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-4cb0ede6b04e5293e2020fe2454429dbc26e23d959ad31472d62293a2a8864893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Case-Control Studies</topic><topic>Diabetic macular edema</topic><topic>Diabetic retinopathy</topic><topic>Diabetic Retinopathy - genetics</topic><topic>Eye Proteins - genetics</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Interaction</topic><topic>Linkage Disequilibrium - genetics</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nerve Growth Factors - genetics</topic><topic>Pigment epithelium-derived factor gene</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Serpins - genetics</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iizuka, Hiroyuki</creatorcontrib><creatorcontrib>Awata, Takuya</creatorcontrib><creatorcontrib>Osaki, Masataka</creatorcontrib><creatorcontrib>Neda, Tamotsu</creatorcontrib><creatorcontrib>Kurihara, Susumu</creatorcontrib><creatorcontrib>Inoue, Kiyoaki</creatorcontrib><creatorcontrib>Inukai, Kouichi</creatorcontrib><creatorcontrib>Kabasawa, Sho</creatorcontrib><creatorcontrib>Mori, Keisuke</creatorcontrib><creatorcontrib>Yoneya, Shin</creatorcontrib><creatorcontrib>Katayama, Shigehiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</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>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iizuka, Hiroyuki</au><au>Awata, Takuya</au><au>Osaki, Masataka</au><au>Neda, Tamotsu</au><au>Kurihara, Susumu</au><au>Inoue, Kiyoaki</au><au>Inukai, Kouichi</au><au>Kabasawa, Sho</au><au>Mori, Keisuke</au><au>Yoneya, Shin</au><au>Katayama, Shigehiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Promoter polymorphisms of the pigment epithelium-derived factor gene are associated with diabetic retinopathy</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2007-09-21</date><risdate>2007</risdate><volume>361</volume><issue>2</issue><spage>421</spage><epage>426</epage><pages>421-426</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Pigment epithelium-derived factor (PEDF or SERPINF1), a neuroprotective and anti-angiogenic factor, may play an important role in the pathogenesis of diabetic retinopathy (DR). In 416 patients with type 2 diabetes, four polymorphisms in the PEDF SNPs were identified, rs12150053 and rs12948385 in the promoter region, rs9913583 in the 5′-untranslated region, and rs1136287 (Met72Thr) in exon 3. Based on case-control studies, rs12150053 and rs12948385, but not rs9913583 and rs1136287, were significantly associated with DR. A logistic regression analysis revealed that the TC or CC genotype of rs12150053 was a significant risk factor for DR (odds ratio 2.40, p=0.0004). The GA or AA genotype of rs12948385 was also a significant risk factor for DR. In addition, a significant interaction between the vascular endothelial growth factor (VEGF) and PEDF SNPs in the susceptibility to DR was found. These results demonstrate that the PEDF gene, in cooperation with the VEGF gene, may contribute to the development of DR.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>17658465</pmid><doi>10.1016/j.bbrc.2007.07.025</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Case-Control Studies Diabetic macular edema Diabetic retinopathy Diabetic Retinopathy - genetics Eye Proteins - genetics Female Genetic Predisposition to Disease Haplotypes Humans Interaction Linkage Disequilibrium - genetics Logistic Models Male Middle Aged Nerve Growth Factors - genetics Pigment epithelium-derived factor gene Polymorphism, Single Nucleotide - genetics Promoter Regions, Genetic - genetics Serpins - genetics Vascular endothelial growth factor Vascular Endothelial Growth Factor A - genetics |
title | Promoter polymorphisms of the pigment epithelium-derived factor gene are associated with diabetic retinopathy |
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