Genetic predictors of sick sinus syndrome
Autor: | Timur R. Nasibullin, Vladimir V. Plechev, Ildus Sagitov, Yanina Timasheva, L. Z. Akhmadishina, Marat Rifkatovich Badykov, Elena Badykova, Naufal Zagidullin, Alfiya Pushkareva |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
medicine.medical_specialty CLCNKA biology Sinoatrial node Sinoatrial block business.industry General Medicine medicine.disease Sick sinus syndrome SSS 03 medical and health sciences 030104 developmental biology 0302 clinical medicine medicine.anatomical_structure 030220 oncology & carcinogenesis Internal medicine Genetic model Genetics medicine biology.protein Prospective cohort study business Molecular Biology Genotyping |
Zdroj: | Molecular Biology Reports. 48:5355-5362 |
ISSN: | 1573-4978 0301-4851 |
DOI: | 10.1007/s11033-021-06517-4 |
Popis: | Sick sinus syndrome (SSS) encompasses a group of conduction disorders characterized by the inability of sinoatrial node to perform its pacemaker function. Our aim was to identify genetic predictors of SSS in a prospective cohort of patients admitted to the clinic for pacemaker implantation using single-locus and multilocus approaches. We performed genotyping for polymorphic markers of CLCNKA (rs10927887), SCN10A (rs6795970), FNDC3B (rs9647379), MIR146A (rs2910164), SYT10 (rs7980799), MYH6 (rs365990), and KCNE1 (rs1805127) genes in the group of 284 patients with SSS and 243 healthy individuals. Associations between the studied loci and SSS were tested using logistic regression under recessive genetic model using sex and age as covariates. Multilocus analysis was performed using Markov chain Monte Carlo method implemented in the APSampler program. Correction for multiple testing was performed using Benjamini–Hochberg procedure. We detected an individual association between KCNE1 rs1805127*A allele and SSS in the total study group (OR 0.43, PFDR = 0.028) and in the subgroup of patients with 2nd or 3rd degree sinoatrial block (OR 0.17, PFDR = 0.033), and identified seven allelic patterns associated with the disease. SCN10A rs6795970*T and MIR146A rs2910164*C alleles were present in all seven combinations associated with SSS. The highest risk of SSS was conferred by the combination SCN10A rs6795970*T+FNDC3B rs9647379*C+MIR146A rs2910164*C+SYT10 rs7980799*C+KCNE1 rs1805127*G (OR 2.98, CI 1.77–5.00, P = 1.27 × 10–5, PFDR = 0.022). Our findings suggest that KCNE1 rs1805127 polymorphism may play a role in susceptibility to sinoatrial node dysfunction, particularly presenting as 2nd or 3rd degree sinoatrial block, and the risk-modifying effect of other studied loci is better detected using multilocus approach. |
Databáze: | OpenAIRE |
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