Candidate gene analysis of 21q22: Support for S100B as a susceptibility gene for bipolar affective disorder with psychosis

• Published in: American journal of medical genetics. Part B, Neuropsychiatric genetics Vol. 144B; no. 8; pp. 1094 - 1096
• Main Authors: Roche, S., Cassidy, F., Zhao, C., Badger, J., Claffey, E., Mooney, L., Delaney, C., Dobrin, S., McKeon, P.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 05.12.2007; Wiley-Liss
• Subjects: Adult and adolescent clinical studies; association; Biological and medical sciences; Bipolar Disorder - genetics; Bipolar disorders; Chromosomes, Human, Pair 21 - genetics; disease variant; DNA - chemistry; DNA - genetics; Genetic Predisposition to Disease - genetics; haplotype; Haplotypes - genetics; Humans; linkage; Linkage Disequilibrium; Medical genetics; Medical sciences; Mood disorders; Polymorphism, Single Nucleotide; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Psychoses; Psychotic Disorders - genetics; Schizophrenia; single nucleotide polymorphisms (SNPs); TRPM2; Genetic mapping; Mood disorder; Disease; Protein S 100B; Pathogenesis; disease variant; Schizophrenia; Bipolar disorder; association; Affective psychosis; linkage; Genetic determinism; Affective disorder; Variant; TRPM2; Sensitivity; single nucleotide polymorphisms (SNPs); Genetic linkage; Predisposition; Genetics; Single nucleotide polymorphism; Haplotype
• ISSN: 1552-4841; 1552-485X
• DOI: 10.1002/ajmg.b.30556

A genome‐wide scan in 60 bipolar affective disorder (BPAD) affected sib‐pairs (ASPs) identified linkage on chromosome 21 at 21q22 (D21S1446, NPL = 1.42, P = 0.08), a BPAD susceptibility locus supported by multiple studies. Although this linkage only approaches significance, the peak marker is located 12 Kb upstream of S100B, a neurotrophic factor implicated in the pathology of psychiatric disorders, including BPAD and schizophrenia. We hypothesized that the linkage signal at 21q22 may result from pathogenic disease variants within S100B and performed an association analysis of this gene in a collection of 125 BPAD type I trios. S100B single nucleotide polymorphisms (SNPs) rs2839350 (P = 0.022) and rs3788266 (P = 0.031) were significantly associated with BPAD. Since variants within S100B have also been associated with schizophrenia susceptibility, we reanalyzed the data in trios with a history of psychosis, a phenotype in common between the two disorders. SNPs rs2339350 (P = 0.016) and rs3788266 (P = 0.009) were more significantly associated in the psychotic subset. Increased significance was also obtained at the haplotype level. Interestingly, SNP rs3788266 is located within a consensus‐binding site for Six‐family transcription factors suggesting that this variant may directly affect S100B gene expression. Fine‐mapping analyses of 21q22 have previously identified transient receptor potential gene melastatin 2 (TRPM2), which is 2 Mb upstream of S100B, as a possible BPAD susceptibility gene at 21q22. We also performed a family‐based association analysis of TRPM2 which did not reveal any evidence for association of this gene with BPAD. Overall, our findings suggest that variants within the S100B gene predispose to a psychotic subtype of BPAD, possibly via alteration of gene expression. © 2007 Wiley‐Liss, Inc.