the daoag30 locus and affective disorders haplotype based association study in a polydiagnostic approachdaoag30轨迹和情感性精神障碍协会研究polydiagnostic方法为基础的单体型.pdf

Gawlik et al. BMC Psychiatry 2010, 10:59 /1471-244X/10/59 RESEARCH ARTICLE Open Access The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach 1* 1 4 3 1 2 Micha Gawlik , Ingeborg Wehner , Meinhard Mende , Sven Jung , Bruno Pfuhlmann , Michael Knapp , Gerald Stöber1 Abstract Background: The DAOA/G30 (D-amino acid oxidase activator) gene complex at chromosomal region 13q32-33 is one of the most intriguing susceptibility loci for the major psychiatric disorders, although there is no consensus about the specific risk alleles or haplotypes across studies. Methods: In a case-control sample of German descent (affective psychosis: n = 248; controls: n = 188) we examined seven single nucleotide polymorphisms (SNPs) around DAOA/G30 (rs3916966, rs1935058, rs2391191, rs1935062, rs947267, rs3918342, and rs9558575) for genetic association in a polydiagnostic approach (ICD 10; Leonhard’s classification). Results: No single marker showed evidence of overall association with affective disorder neither in ICD10 nor Leonhard’s classification. Haplotype analysis revealed no association with recurrent unipolar depression or bipolar disorder according to ICD10, within Leonhard’s classification manic-depression was associated with a 3-locus haplotype (rs2391191, rs1935062, and rs3916966; P = 0.022) and monopolar depression with a 5-locus combination at the DAOA/G30 core region (P = 0.036). Conclusion: Our data revealed potential evidence for partially overlapping risk haplotypes at the DAOA/G30 locus in Leonhard’s affective psychoses, but do not support a common genetic contribution of the DAOA/G30 gene complex to the pathogenesis of affective disorders. Background