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The role of sodium channels in sudden unexpected death in pediatrics

BACKGROUND: Sudden Unexpected Death in Pediatrics (SUDP) is a tragic event, likely caused by the complex interaction of multiple factors. The presence of hippocampal abnormalities in many children with SUDP suggests that epilepsy‐related mechanisms may contribute to death, similar to Sudden Unexplai...

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Autores principales: Rochtus, Anne M., Goldstein, Richard D., Holm, Ingrid A., Brownstein, Catherine A., Pérez‐Palma, Eduardo, Haynes, Robin, Lal, Dennis, Poduri, Annapurna H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434613/
https://www.ncbi.nlm.nih.gov/pubmed/32449611
http://dx.doi.org/10.1002/mgg3.1309
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author Rochtus, Anne M.
Goldstein, Richard D.
Holm, Ingrid A.
Brownstein, Catherine A.
Pérez‐Palma, Eduardo
Haynes, Robin
Lal, Dennis
Poduri, Annapurna H.
author_facet Rochtus, Anne M.
Goldstein, Richard D.
Holm, Ingrid A.
Brownstein, Catherine A.
Pérez‐Palma, Eduardo
Haynes, Robin
Lal, Dennis
Poduri, Annapurna H.
author_sort Rochtus, Anne M.
collection PubMed
description BACKGROUND: Sudden Unexpected Death in Pediatrics (SUDP) is a tragic event, likely caused by the complex interaction of multiple factors. The presence of hippocampal abnormalities in many children with SUDP suggests that epilepsy‐related mechanisms may contribute to death, similar to Sudden Unexplained Death in Epilepsy. Because of known associations between the genes SCN1A and SCN5A and sudden death, and shared mechanisms and patterns of expression in genes encoding many voltage‐gated sodium channels (VGSCs), we hypothesized that individuals dying from SUDP have pathogenic variants across the entire family of cardiac arrhythmia‐ and epilepsy‐associated VGSC genes. METHODS: To address this hypothesis, we evaluated whole‐exome sequencing data from infants and children with SUDP for variants in VGSC genes, reviewed the literature for all SUDP‐associated variants in VGSCs, applied a novel paralog analysis to all variants, and evaluated all variants according to American College of Medical Genetics and Genomics (ACMG) guidelines. RESULTS: In our cohort of 73 cases of SUDP, we assessed 11 variants as pathogenic in SCN1A, SCN1B, and SCN10A, genes with long‐standing disease associations, and in SCN3A, SCN4A, and SCN9A, VGSC gene paralogs with more recent disease associations. From the literature, we identified 82 VGSC variants in SUDP cases. Pathogenic variants clustered at conserved amino acid sites intolerant to variation across the VGSC genes, which is unlikely to occur in the general population (p < .0001). For 54% of variants previously reported in literature, we identified conflicting evidence regarding pathogenicity when applying ACMG criteria and modern population data. CONCLUSION: We report variants in several VGSC genes in cases with SUDP, involving both arrhythmia‐ and epilepsy‐associated genes. Accurate variant assessment as well as future studies are essential for an improved understanding of the contribution of sodium channel‐related variants to SUDP.
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spelling pubmed-74346132020-08-20 The role of sodium channels in sudden unexpected death in pediatrics Rochtus, Anne M. Goldstein, Richard D. Holm, Ingrid A. Brownstein, Catherine A. Pérez‐Palma, Eduardo Haynes, Robin Lal, Dennis Poduri, Annapurna H. Mol Genet Genomic Med Original Articles BACKGROUND: Sudden Unexpected Death in Pediatrics (SUDP) is a tragic event, likely caused by the complex interaction of multiple factors. The presence of hippocampal abnormalities in many children with SUDP suggests that epilepsy‐related mechanisms may contribute to death, similar to Sudden Unexplained Death in Epilepsy. Because of known associations between the genes SCN1A and SCN5A and sudden death, and shared mechanisms and patterns of expression in genes encoding many voltage‐gated sodium channels (VGSCs), we hypothesized that individuals dying from SUDP have pathogenic variants across the entire family of cardiac arrhythmia‐ and epilepsy‐associated VGSC genes. METHODS: To address this hypothesis, we evaluated whole‐exome sequencing data from infants and children with SUDP for variants in VGSC genes, reviewed the literature for all SUDP‐associated variants in VGSCs, applied a novel paralog analysis to all variants, and evaluated all variants according to American College of Medical Genetics and Genomics (ACMG) guidelines. RESULTS: In our cohort of 73 cases of SUDP, we assessed 11 variants as pathogenic in SCN1A, SCN1B, and SCN10A, genes with long‐standing disease associations, and in SCN3A, SCN4A, and SCN9A, VGSC gene paralogs with more recent disease associations. From the literature, we identified 82 VGSC variants in SUDP cases. Pathogenic variants clustered at conserved amino acid sites intolerant to variation across the VGSC genes, which is unlikely to occur in the general population (p < .0001). For 54% of variants previously reported in literature, we identified conflicting evidence regarding pathogenicity when applying ACMG criteria and modern population data. CONCLUSION: We report variants in several VGSC genes in cases with SUDP, involving both arrhythmia‐ and epilepsy‐associated genes. Accurate variant assessment as well as future studies are essential for an improved understanding of the contribution of sodium channel‐related variants to SUDP. John Wiley and Sons Inc. 2020-05-25 /pmc/articles/PMC7434613/ /pubmed/32449611 http://dx.doi.org/10.1002/mgg3.1309 Text en © 2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rochtus, Anne M.
Goldstein, Richard D.
Holm, Ingrid A.
Brownstein, Catherine A.
Pérez‐Palma, Eduardo
Haynes, Robin
Lal, Dennis
Poduri, Annapurna H.
The role of sodium channels in sudden unexpected death in pediatrics
title The role of sodium channels in sudden unexpected death in pediatrics
title_full The role of sodium channels in sudden unexpected death in pediatrics
title_fullStr The role of sodium channels in sudden unexpected death in pediatrics
title_full_unstemmed The role of sodium channels in sudden unexpected death in pediatrics
title_short The role of sodium channels in sudden unexpected death in pediatrics
title_sort role of sodium channels in sudden unexpected death in pediatrics
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434613/
https://www.ncbi.nlm.nih.gov/pubmed/32449611
http://dx.doi.org/10.1002/mgg3.1309
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