Key result
A genome-wide association study found no single nucleotide polymorphisms with genome-wide significant association to sinus bradycardia induced by second-generation antipsychotics, with the top hit rs1275749 showing an odds ratio of 9.622.
Why the study?
Sinus bradycardia can be induced by second-generation antipsychotics in schizophrenia patients, but the roles of genetic factors have not been studied.
What genetic variants are associated with sinus bradycardia induced by second-generation antipsychotics in Han Chinese schizophrenia patients?
Case-Control (n=88)
No
What genetic variants are associated with sinus bradycardia induced by second-generation antipsychotics in Han Chinese schizophrenia patients?
Odds Ratio: 9.622 (95% CI 3.069–30.17)
p-value: p=0.0001032
This preliminary GWAS did not identify genome-wide significant SNPs for SGA-induced sinus bradycardia in Han Chinese schizophrenia patients, but suggests CTNNA3 as a possible susceptibility gene.
No genome-wide significant loci for SGA-induced bradycardia; leaves open the genetic basis and requires larger studies.
Second-generation antipsychotics (SGAs) play a critical role in current treatment of schizophrenia (SCZ). It has been observed that sinus bradycardia, rare but in certain situations life threatening adverse drug reaction, can be induced by SGAs across different schizophrenia populations. However, the roles of genetic factors in this phenomenon have not been studied yet. In the present study, a genome-wide association study of single nucleotide polymorphisms (SNPs) was performed on Chinese Han SCZ patients to identify susceptibility loci that were associated with sinus bradycardia induced by SGAs. This study applied microarray to obtain genotype profiles of 88 Han Chinese SCZ patients. Our results found that there were no SNPs had genome-wide significant association with sinus bradycardia induced by SGAs. The top GWAS hit located in gene KIAA0247, which mainly regulated by the tumor suppressor P53 and thus plays a role in carcinogenesis based on resent research and it should not be a susceptibility locus to sinus bradycardia induced by SGAs. Using gene-set functional analysis, we tested that if top 500 SNPs mapped genes were relevant to sinus bradycardia. The result of gene prioritization analysis showed CTNNA3 was strongly correlated with sinus bradycardia, hinting it was a susceptibility gene of this ADR. Our study provides a preliminary study of genetic variants associated with sinus bradycardia induced by SGAs in Han Chinese SCZ patients. The discovery of a possible susceptibility gene shed light on further study of this adverse drug reaction in Han Chinese SCZ patients.
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Weng et al. (2021) conducted a case-control in Schizophrenia with antipsychotic-induced sinus bradycardia (n=88). Second-generation antipsychotics vs. Patients taking second-generation antipsychotics without sinus bradycardia was evaluated on Association of SNP rs1275749 with sinus bradycardia (OR 9.622, 95% CI 3.069-30.17, p=0.0001032). A genome-wide association study found no single nucleotide polymorphisms with genome-wide significant association to sinus bradycardia induced by second-generation antipsychotics, with the top hit rs1275749 showing an odds ratio of 9.622.
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