Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia

0554797 - BTÚ 2022 RIV CH eng J - Článek v odborném periodiku
Hirschfeldova, K. - Černý, Jiří - Božíková, Paulina - Kuchtiak, V. - Rausch, T. - Benes, V. - Španiel, F. - Greguš, D. - Horáček, J. - Vyklický, L. - Balik, A.
Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia.
Journal of Personalized Medicine. Roč. 11, č. 12 (2021), č. článku 1250. E-ISSN 2075-4426
Institucionální podpora: RVO:86652036
Klíčová slova: polygenic risk score * subunit gene grin1 * synaptic plasticity * population-structure
Obor OECD: Substance abuse
Impakt faktor: 3.508, rok: 2021
Způsob publikování: Open access
https://www.mdpi.com/2075-4426/11/12/1250

The heritable component of schizophrenia (SCH) as a polygenic trait is represented by numerous variants from a heterogeneous group of genes each contributing a relatively small effect. Various SNPs have already been found and analyzed in genes encoding the NMDAR subunits. However, less is known about genetic variations of genes encoding the AMPA and kainate receptor subunits. We analyzed sixteen iGluR genes in full length to determine the sequence variability of iGluR genes. Our aim was to describe the rate of genetic variability, its distribution, and the co-occurrence of variants and to identify new candidate risk variants or haplotypes. The cumulative effect of genetic risk was then estimated using a simple scoring model. GRIN2A-B, GRIN3A-B, and GRIK4 genes showed significantly increased genetic variation in SCH patients. The fixation index statistic revealed eight intronic haplotypes and an additional four intronic SNPs within the sequences of iGluR genes associated with SCH (p < 0.05). The haplotypes were used in the proposed simple scoring model and moreover as a test for genetic predisposition to schizophrenia. The positive likelihood ratio for the scoring model test reached 7.11. We also observed 41 protein-altering variants (38 missense variants, four frameshifts, and one nonsense variant) that were not significantly associated with SCH. Our data suggest that some intronic regulatory regions of iGluR genes and their common variability are among the components from which the genetic predisposition to SCH is composed.
Trvalý link: http://hdl.handle.net/11104/0329540