1. Genetic analysis of the ZNF804A gene in Mexican patients with schizophrenia, schizoaffective disorder and bipolar disorder
- Author
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Lucía Münch-Anguiano, Beatriz Camarena, Jesica Nieto-Quinto, Patricia de la Torre, Juan Pedro Laclette, Harumi Hirata-Hernández, Sandra Hernández-Muñoz, Alejandro Aguilar-García, Claudia Becerra-Palars, Doris Gutiérrez-Mora, Hiram Ortega-Ortiz, Raúl Escamilla-Orozco, Ricardo Saracco-Álvarez, and Ismael Bustos-Jaimes
- Subjects
Bipolar Disorder ,Psychotic Disorders ,Genetics ,Kruppel-Like Transcription Factors ,Schizophrenia ,Humans ,Genetic Predisposition to Disease ,General Medicine ,Mexico ,Polymorphism, Single Nucleotide - Abstract
Evidence suggests that schizophrenia (SCZ), schizoaffective disorder (SAD) and bipolar disorder (BPD) share genetic risk variants. ZNF804A gene has been associated with these disorders in different populations. GWAS and candidate gene studies have reported association between the rs1344706 A allele with SCZ, SAD and BPD in European and Asian populations. In Mexican patients, no studies have specifically analyzed ZNF804A gene variants with these disorders. The aim of the study was to analyze the rs1344706 and identify common and rare variants in a targeted region of the ZNF804A gene in Mexican patients with SCZ, BPD and SAD compared with a control group.We genotyped the rs1344706 in 228 Mexican patients diagnosed with SCZ, SAD and BPD, and 295 controls. Also, an additional sample of 167 patients with these disorders and 170 controls was analyzed to identify rare and common variants using the Sanger-sequence analysis of a targeted region of ZNF804A gene.Association analysis of rs1344706 observed a higher frequency of A allele in the patients compared with the control group; however, did not show statistical differences after Bonferronís correction (χ2 = 5.3, p = 0.0208). In the sequence analysis, we did not identify rare variants; however, we identified three common variants: rs3046266, rs1366842 and rs12477430. A comparison of the three identified variants between patients and controls did not show statistical differences (p 0.0125). Finally, haplotype analysis did not show statistical differences between SCZ, SAD and BPD and controls.Our findings did not support the evidence suggesting that ZNF804A gene participates in the etiology of SCZ, SAD and BPD. Future studies are needed in a larger sample size to identify the effect of this gene in psychiatric disorders.
- Published
- 2021