Functional PAX-6 gene-linked polymorphic region: potential association with paranoid schizophrenia
Background: Early differentiation of the nervous system and adult CNS neuroplasticity is modulated by PAX-6. We have shown previously that a highly polymorphic, functional AC/AG repeat in the 5′ regulatory region of the gene showed significantly increased promoter activity, if containing ≥ 29 repeat...
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creator | Stöber, Gerald Syagailo, Yana V Okladnova, Olga Jungkunz, Gerd Knapp, Michael Beckmann, Helmut Lesch, Klaus-Peter |
description | Background: Early differentiation of the nervous system and adult CNS neuroplasticity is modulated by PAX-6. We have shown previously that a highly polymorphic, functional AC/AG repeat in the 5′ regulatory region of the gene showed significantly increased promoter activity, if containing ≥ 29 repeats, and that the heterozygous genotype (≤ 28/≥ 29) revealed increased mRNA PAX-6 levels in human brain tissue compared to the homozygous short variant.
Methods: In a case-control study of 655 unrelated individuals, allele frequencies and genotype distributions of the functional PAX-6 promoter polymorphism were investigated comprising patients with DSM-IV schizophrenia, patients with affective disorders, and population controls.
Results: No allelic or genotypic association of the PAX-6 promoter polymorphism to affective disorder or to schizophrenia as one disease entity was observed. After subtyping schizophrenia into paranoid and nonparanoid forms, potential evidence was found for a genotypic association of the high-activity variant with the paranoid subtype of schizophrenia (p = .02). The estimated odds ratio was 1.7 (95% CI .98 to 2.95) for those heterozygous and 1.4 (95% CI .82 to 2.42) for those heterozygous or homozygous for the high-activity variant compared to the homozygous low-activity variant.
Conclusions: Our finding indicates that early developmental genes may be involved in the etiopathogenesis of schizophrenia subtypes via variable transcriptional regulation in the developing and adult human brain. |
doi_str_mv | 10.1016/S0006-3223(99)00024-4 |
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Methods: In a case-control study of 655 unrelated individuals, allele frequencies and genotype distributions of the functional PAX-6 promoter polymorphism were investigated comprising patients with DSM-IV schizophrenia, patients with affective disorders, and population controls.
Results: No allelic or genotypic association of the PAX-6 promoter polymorphism to affective disorder or to schizophrenia as one disease entity was observed. After subtyping schizophrenia into paranoid and nonparanoid forms, potential evidence was found for a genotypic association of the high-activity variant with the paranoid subtype of schizophrenia (p = .02). The estimated odds ratio was 1.7 (95% CI .98 to 2.95) for those heterozygous and 1.4 (95% CI .82 to 2.42) for those heterozygous or homozygous for the high-activity variant compared to the homozygous low-activity variant.
Conclusions: Our finding indicates that early developmental genes may be involved in the etiopathogenesis of schizophrenia subtypes via variable transcriptional regulation in the developing and adult human brain.</description><identifier>ISSN: 0006-3223</identifier><identifier>EISSN: 1873-2402</identifier><identifier>DOI: 10.1016/S0006-3223(99)00024-4</identifier><identifier>PMID: 10376119</identifier><identifier>CODEN: BIPCBF</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Adult and adolescent clinical studies ; Alleles ; Biological and medical sciences ; bipolar affective disorder ; Bipolar Disorder - genetics ; Brain - cytology ; Case-Control Studies ; Culture Techniques ; Female ; gene ; Genes, Regulator - genetics ; Genetic Linkage - genetics ; Genetic Variation - genetics ; Genotype ; Heterozygote ; Humans ; linkage ; Male ; Medical sciences ; Middle Aged ; neurodevelopment ; Neuronal Plasticity - genetics ; PAX-6 ; Point Mutation - genetics ; polymorphism ; Polymorphism, Genetic - genetics ; promoter ; Promoter Regions, Genetic - genetics ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychoses ; repeat ; RNA, Messenger - genetics ; Schizophrenia ; Schizophrenia, Paranoid - genetics ; Transcription, Genetic - genetics</subject><ispartof>Biological psychiatry (1969), 1999-06, Vol.45 (12), p.1585-1591</ispartof><rights>1999 Society of Biological Psychiatry</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-78af0acd8302c1600d9824a96e4283db3d946c292f3cdaa21eedf938f3a21d783</citedby><cites>FETCH-LOGICAL-c419t-78af0acd8302c1600d9824a96e4283db3d946c292f3cdaa21eedf938f3a21d783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006322399000244$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1877114$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10376119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stöber, Gerald</creatorcontrib><creatorcontrib>Syagailo, Yana V</creatorcontrib><creatorcontrib>Okladnova, Olga</creatorcontrib><creatorcontrib>Jungkunz, Gerd</creatorcontrib><creatorcontrib>Knapp, Michael</creatorcontrib><creatorcontrib>Beckmann, Helmut</creatorcontrib><creatorcontrib>Lesch, Klaus-Peter</creatorcontrib><title>Functional PAX-6 gene-linked polymorphic region: potential association with paranoid schizophrenia</title><title>Biological psychiatry (1969)</title><addtitle>Biol Psychiatry</addtitle><description>Background: Early differentiation of the nervous system and adult CNS neuroplasticity is modulated by PAX-6. We have shown previously that a highly polymorphic, functional AC/AG repeat in the 5′ regulatory region of the gene showed significantly increased promoter activity, if containing ≥ 29 repeats, and that the heterozygous genotype (≤ 28/≥ 29) revealed increased mRNA PAX-6 levels in human brain tissue compared to the homozygous short variant.
Methods: In a case-control study of 655 unrelated individuals, allele frequencies and genotype distributions of the functional PAX-6 promoter polymorphism were investigated comprising patients with DSM-IV schizophrenia, patients with affective disorders, and population controls.
Results: No allelic or genotypic association of the PAX-6 promoter polymorphism to affective disorder or to schizophrenia as one disease entity was observed. After subtyping schizophrenia into paranoid and nonparanoid forms, potential evidence was found for a genotypic association of the high-activity variant with the paranoid subtype of schizophrenia (p = .02). The estimated odds ratio was 1.7 (95% CI .98 to 2.95) for those heterozygous and 1.4 (95% CI .82 to 2.42) for those heterozygous or homozygous for the high-activity variant compared to the homozygous low-activity variant.
Conclusions: Our finding indicates that early developmental genes may be involved in the etiopathogenesis of schizophrenia subtypes via variable transcriptional regulation in the developing and adult human brain.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>bipolar affective disorder</subject><subject>Bipolar Disorder - genetics</subject><subject>Brain - cytology</subject><subject>Case-Control Studies</subject><subject>Culture Techniques</subject><subject>Female</subject><subject>gene</subject><subject>Genes, Regulator - genetics</subject><subject>Genetic Linkage - genetics</subject><subject>Genetic Variation - genetics</subject><subject>Genotype</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>linkage</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>neurodevelopment</subject><subject>Neuronal Plasticity - genetics</subject><subject>PAX-6</subject><subject>Point Mutation - genetics</subject><subject>polymorphism</subject><subject>Polymorphism, Genetic - genetics</subject><subject>promoter</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>repeat</subject><subject>RNA, Messenger - genetics</subject><subject>Schizophrenia</subject><subject>Schizophrenia, Paranoid - genetics</subject><subject>Transcription, Genetic - genetics</subject><issn>0006-3223</issn><issn>1873-2402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhq2qqAnQn0C1hwrBYcFfeG0uKIr4kpCKRCv1Zjn2bOJ2Yy_2BkR_PQ6J2t44zYz1vDPWg9ABwScEE3H6gDEWNaOUHSl1XAbKa_4BjYlsWE05ph_R-C8yQrs5_ypjQyn5hEYEs0YQosZodrUKdvAxmK66n_ysRTWHAHXnw29wVR-7l2VM_cLbKsG8YOflbYAw-MKbnKP1Zp2unv2wqHqTTIjeVdku_J_YLxIEb_bRTmu6DJ-3dQ_9uLr8Pr2p775d304nd7XlRA11I02LjXWSYWqJwNgpSblRAjiVzM2YU1xYqmjLrDOGEgDXKiZbVnrXSLaHDjd7-xQfV5AHvfTZQteZAHGVtVCScSFZAc82oE0x5wSt7pNfmvSiCdZrufpNrl6b00rpN7mal9yX7YHVbAnuv9TGZgG-bgGTrenaYsP6_I-TTUPIes_FBoNi48lD0tl6CBacT2AH7aJ_5yevbNyXCg</recordid><startdate>19990615</startdate><enddate>19990615</enddate><creator>Stöber, Gerald</creator><creator>Syagailo, Yana V</creator><creator>Okladnova, Olga</creator><creator>Jungkunz, Gerd</creator><creator>Knapp, Michael</creator><creator>Beckmann, Helmut</creator><creator>Lesch, Klaus-Peter</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><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></search><sort><creationdate>19990615</creationdate><title>Functional PAX-6 gene-linked polymorphic region: potential association with paranoid schizophrenia</title><author>Stöber, Gerald ; Syagailo, Yana V ; Okladnova, Olga ; Jungkunz, Gerd ; Knapp, Michael ; Beckmann, Helmut ; Lesch, Klaus-Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-78af0acd8302c1600d9824a96e4283db3d946c292f3cdaa21eedf938f3a21d783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Alleles</topic><topic>Biological and medical sciences</topic><topic>bipolar affective disorder</topic><topic>Bipolar Disorder - genetics</topic><topic>Brain - cytology</topic><topic>Case-Control Studies</topic><topic>Culture Techniques</topic><topic>Female</topic><topic>gene</topic><topic>Genes, Regulator - genetics</topic><topic>Genetic Linkage - genetics</topic><topic>Genetic Variation - genetics</topic><topic>Genotype</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>linkage</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>neurodevelopment</topic><topic>Neuronal Plasticity - genetics</topic><topic>PAX-6</topic><topic>Point Mutation - genetics</topic><topic>polymorphism</topic><topic>Polymorphism, Genetic - genetics</topic><topic>promoter</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>repeat</topic><topic>RNA, Messenger - genetics</topic><topic>Schizophrenia</topic><topic>Schizophrenia, Paranoid - genetics</topic><topic>Transcription, Genetic - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stöber, Gerald</creatorcontrib><creatorcontrib>Syagailo, Yana V</creatorcontrib><creatorcontrib>Okladnova, Olga</creatorcontrib><creatorcontrib>Jungkunz, Gerd</creatorcontrib><creatorcontrib>Knapp, Michael</creatorcontrib><creatorcontrib>Beckmann, Helmut</creatorcontrib><creatorcontrib>Lesch, Klaus-Peter</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Biological psychiatry (1969)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stöber, Gerald</au><au>Syagailo, Yana V</au><au>Okladnova, Olga</au><au>Jungkunz, Gerd</au><au>Knapp, Michael</au><au>Beckmann, Helmut</au><au>Lesch, Klaus-Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional PAX-6 gene-linked polymorphic region: potential association with paranoid schizophrenia</atitle><jtitle>Biological psychiatry (1969)</jtitle><addtitle>Biol Psychiatry</addtitle><date>1999-06-15</date><risdate>1999</risdate><volume>45</volume><issue>12</issue><spage>1585</spage><epage>1591</epage><pages>1585-1591</pages><issn>0006-3223</issn><eissn>1873-2402</eissn><coden>BIPCBF</coden><abstract>Background: Early differentiation of the nervous system and adult CNS neuroplasticity is modulated by PAX-6. We have shown previously that a highly polymorphic, functional AC/AG repeat in the 5′ regulatory region of the gene showed significantly increased promoter activity, if containing ≥ 29 repeats, and that the heterozygous genotype (≤ 28/≥ 29) revealed increased mRNA PAX-6 levels in human brain tissue compared to the homozygous short variant.
Methods: In a case-control study of 655 unrelated individuals, allele frequencies and genotype distributions of the functional PAX-6 promoter polymorphism were investigated comprising patients with DSM-IV schizophrenia, patients with affective disorders, and population controls.
Results: No allelic or genotypic association of the PAX-6 promoter polymorphism to affective disorder or to schizophrenia as one disease entity was observed. After subtyping schizophrenia into paranoid and nonparanoid forms, potential evidence was found for a genotypic association of the high-activity variant with the paranoid subtype of schizophrenia (p = .02). The estimated odds ratio was 1.7 (95% CI .98 to 2.95) for those heterozygous and 1.4 (95% CI .82 to 2.42) for those heterozygous or homozygous for the high-activity variant compared to the homozygous low-activity variant.
Conclusions: Our finding indicates that early developmental genes may be involved in the etiopathogenesis of schizophrenia subtypes via variable transcriptional regulation in the developing and adult human brain.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10376119</pmid><doi>10.1016/S0006-3223(99)00024-4</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Alleles Biological and medical sciences bipolar affective disorder Bipolar Disorder - genetics Brain - cytology Case-Control Studies Culture Techniques Female gene Genes, Regulator - genetics Genetic Linkage - genetics Genetic Variation - genetics Genotype Heterozygote Humans linkage Male Medical sciences Middle Aged neurodevelopment Neuronal Plasticity - genetics PAX-6 Point Mutation - genetics polymorphism Polymorphism, Genetic - genetics promoter Promoter Regions, Genetic - genetics Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses repeat RNA, Messenger - genetics Schizophrenia Schizophrenia, Paranoid - genetics Transcription, Genetic - genetics |
title | Functional PAX-6 gene-linked polymorphic region: potential association with paranoid schizophrenia |
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