Literature DB >> 24072447

Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation.

Jessica T Delaney1, Raafia Muhammad, Yaping Shi, Jonathan S Schildcrout, Marcia Blair, Laura Short, Dan M Roden, Dawood Darbar.   

Abstract

AIMS: SCN10A encodes the sodium channel Nav1.8 implicated by genome-wide association studies as a modulator of atrioventricular conduction (PR interval). In a cohort of patients with atrial fibrillation (AF), we examined whether there was an association between common variants in SCN10A and both the PR interval during normal sinus rhythm and the heart rate response during AF. METHODS AND
RESULTS: Patients prospectively enrolled in the Vanderbilt AF registry with electrocardiograms in normal sinus rhythm and/or AF within 1 year of enrollment were genotyped for two common SCN10A variants rs6795970 and rs12632942. Both variants were associated with the PR interval duration in a gene-dose effect on unadjusted analysis; after adjustment for the covariates age, gender, body mass index, hypertension, congestive heart failure, and medication usage, the association remained for rs6795970 only (P = 0.012, partial R(2) = 0.0139). On unadjusted analysis, heart rate response during AF was associated with rs6795970 (P = 0.035, partial R(2) = 0.015), but not with rs12632942 (P = 0.89), and neither association was significant after adjustment for covariates.
CONCLUSION: The common variant rs6795970 in SCN10A is associated with the PR interval duration among healthy patients and those with AF. In addition, this single nucleotide polymorphism trended towards an association with heart rate response during AF indicating the importance of this common SCN10A polymorphism as a marker of atrioventricular conduction.

Entities:  

Keywords:  Atrial fibrillation; PR interval; SCN10A

Mesh:

Substances:

Year:  2013        PMID: 24072447      PMCID: PMC3977588          DOI: 10.1093/europace/eut278

Source DB:  PubMed          Journal:  Europace        ISSN: 1099-5129            Impact factor:   5.214


  31 in total

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6.  P-wave indices: derivation of reference values from the Framingham Heart Study.

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Journal:  Nat Genet       Date:  2010-01-10       Impact factor: 38.330

8.  Localisation of SCN10A gene product Na(v)1.8 and novel pain-related ion channels in human heart.

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10.  Genome-wide association studies of the PR interval in African Americans.

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1.  Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.

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2.  Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.

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3.  Functional characterization of SCN10A variants in several cases of sudden unexplained death.

Authors:  Ivan Gando; Nori Williams; Glenn I Fishman; Barbara A Sampson; Yingying Tang; William A Coetzee
Journal:  Forensic Sci Int       Date:  2019-05-29       Impact factor: 2.395

4.  Common and rare variants in SCN10A modulate the risk of atrial fibrillation.

Authors:  Javad Jabbari; Morten S Olesen; Lei Yuan; Jonas B Nielsen; Bo Liang; Vincenzo Macri; Ingrid E Christophersen; Nikolaj Nielsen; Ahmad Sajadieh; Patrick T Ellinor; Morten Grunnet; Stig Haunsø; Anders G Holst; Jesper H Svendsen; Thomas Jespersen
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Review 5.  Recent genetic discoveries implicating ion channels in human cardiovascular diseases.

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8.  Neuronal Nav1.8 Channels as a Novel Therapeutic Target of Acute Atrial Fibrillation Prevention.

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9.  Homozygosity for the SCN10A Polymorphism rs6795970 Is Associated With Hypoalgesic Inflammatory Bowel Disease Phenotype.

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Journal:  Front Med (Lausanne)       Date:  2018-11-27

10.  Common variants in SCN10A gene associated with Brugada syndrome.

Authors:  Yan Huang; Xiao-Meng Chen; Hector Barajas-Martinez; Hong Jiang; Charles Antzelevitch; Dan Hu
Journal:  Hum Mol Genet       Date:  2021-12-27       Impact factor: 5.121

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