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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Veröffentlicht in:Biological psychiatry (1969) 1999-06, Vol.45 (12), p.1585-1591
Hauptverfasser: Stöber, Gerald, Syagailo, Yana V, Okladnova, Olga, Jungkunz, Gerd, Knapp, Michael, Beckmann, Helmut, Lesch, Klaus-Peter
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Sprache:eng
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Zusammenfassung: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.
ISSN:0006-3223
1873-2402
DOI:10.1016/S0006-3223(99)00024-4