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Evidence for the Contribution of HCN1 Gene Polymorphism (rs1501357) to Working Memory at Both Behavioral and Neural Levels in Schizophrenia Patients and Healthy Controls

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Date 2022 Aug 20
PMID 35987754
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Abstract

Gene HCN1 polymorphism (rs1501357) has been proposed to be one of the candidate risk genes for schizophrenia in the second report of the Psychiatric Genomics Consortium-Schizophrenia Workgroup. Although animal studies repeatedly showed a role of this gene in working memory, its contribution to working memory in human samples, especially in schizophrenia patients, is still unknown. To explore the association between rs1501357 and working memory at both behavioral (Study 1) and neural (Study 2) levels, the current study involved two independent samples. Study 1 included 876 schizophrenia patients and 842 healthy controls, all of whom were assessed on a 2-back task, a dot pattern expectancy task (DPX), and a digit span task. Study 2 included 56 schizophrenia patients and 155 healthy controls, all of whom performed a 2-back task during functional magnetic resonance imaging (fMRI) scanning. In both studies, we consistently found significant genotype-by-diagnosis interaction effects. For Study 1, the interaction effects were significant for the three tasks. Patients carrying the risk allele performed worse than noncarriers, while healthy controls showed the opposite pattern. For Study 2, the interaction effects were observed at the parietal cortex and the medial frontal cortex. Patients carrying the risk allele showed increased activation at right parietal cortex and increased deactivation at the medial frontal cortex, while healthy controls showed the opposite pattern. These results suggest that the contributions of rs1501357 to working memory capability vary in different populations (i.e., schizophrenia patients vs. healthy controls), which expands our understanding of the functional impact of the HCN1 gene. Future studies should examine its associations with other cognitive functions.

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References
1.
Zhang Z, Yan T, Wang Y, Zhang Q, Zhao W, Chen X . Polymorphism in schizophrenia risk gene is associated with the posterior cingulate Cortex's activation and functional and structural connectivity in healthy controls. Neuroimage Clin. 2018; 19:160-166. PMC: 6051762. DOI: 10.1016/j.nicl.2018.03.039. View

2.
Lencz T, Malhotra A . Targeting the schizophrenia genome: a fast track strategy from GWAS to clinic. Mol Psychiatry. 2015; 20(7):820-6. PMC: 4486648. DOI: 10.1038/mp.2015.28. View

3.
Zhang Q, Li Y, Zhao W, Chen X, Li X, Du B . ERP evidence for the effect of working memory span training on working memory maintenance: A randomized controlled trial. Neurobiol Learn Mem. 2019; 167:107129. DOI: 10.1016/j.nlm.2019.107129. View

4.
Zhang Z, Chen X, Yu P, Zhang Q, Sun X, Gu H . Evidence for the contribution of NOS1 gene polymorphism (rs3782206) to prefrontal function in schizophrenia patients and healthy controls. Neuropsychopharmacology. 2014; 40(6):1383-94. PMC: 4397396. DOI: 10.1038/npp.2014.323. View

5.
Mendrek A, Kiehl K, Smith A, Irwin D, Forster B, Liddle P . Dysfunction of a distributed neural circuitry in schizophrenia patients during a working-memory performance. Psychol Med. 2005; 35(2):187-96. DOI: 10.1017/s0033291704003228. View