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Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients
The objective of this work was to identify genetic variants in Mexican patients diagnosed with hypertrophic cardiomyopathy (HCM). According to world literature, the genes mainly involved are MHY7 and MYBPC3, although variants have been found in more than 50 genes related to heart disease and sudden...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657276/ https://www.ncbi.nlm.nih.gov/pubmed/37498360 http://dx.doi.org/10.1007/s00438-023-02048-8 |
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author | García-Vielma, Catalina Lazalde-Córdova, Luis Gerardo Arzola-Hernández, José Cruz González-Aceves, Erick Noel López-Zertuche, Herminio Guzmán-Delgado, Nancy Elena González-Salazar, Francisco |
author_facet | García-Vielma, Catalina Lazalde-Córdova, Luis Gerardo Arzola-Hernández, José Cruz González-Aceves, Erick Noel López-Zertuche, Herminio Guzmán-Delgado, Nancy Elena González-Salazar, Francisco |
author_sort | García-Vielma, Catalina |
collection | PubMed |
description | The objective of this work was to identify genetic variants in Mexican patients diagnosed with hypertrophic cardiomyopathy (HCM). According to world literature, the genes mainly involved are MHY7 and MYBPC3, although variants have been found in more than 50 genes related to heart disease and sudden death, and to our knowledge there are no studies in the Mexican population. These variants are reported and classified in the ClinVar (PubMed) database and only some of them are recognized in the Online Mendelian Information in Men (OMIM). The present study included 37 patients, with 14 sporadic cases and 6 familial cases, with a total of 21 index cases. Next-generation sequencing was performed on a predesigned panel of 168 genes associated with heart disease and sudden death. The sequencing analysis revealed twelve (57%) pathogenic or probably pathogenic variants, 9 of them were familial cases, managing to identify pathogenic variants in relatives without symptoms of the disease. At the molecular level, nine of the 12 variants (75%) were single nucleotide changes, 2 (17%) deletions, and 1 (8%) splice site alteration. The genes involved were MYH7 (25%), MYBPC3 (25%) and ACADVL, KCNE1, TNNI3, TPM1, SLC22A5, TNNT2 (8%). In conclusion; we found five variants that were not previously reported in public databases. It is important to follow up on the reclassification of variants, especially those of uncertain significance in patients with symptoms of the condition. All patients included in the study and their relatives received family genetic counseling. |
format | Online Article Text |
id | pubmed-10657276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-106572762023-07-27 Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients García-Vielma, Catalina Lazalde-Córdova, Luis Gerardo Arzola-Hernández, José Cruz González-Aceves, Erick Noel López-Zertuche, Herminio Guzmán-Delgado, Nancy Elena González-Salazar, Francisco Mol Genet Genomics Original Article The objective of this work was to identify genetic variants in Mexican patients diagnosed with hypertrophic cardiomyopathy (HCM). According to world literature, the genes mainly involved are MHY7 and MYBPC3, although variants have been found in more than 50 genes related to heart disease and sudden death, and to our knowledge there are no studies in the Mexican population. These variants are reported and classified in the ClinVar (PubMed) database and only some of them are recognized in the Online Mendelian Information in Men (OMIM). The present study included 37 patients, with 14 sporadic cases and 6 familial cases, with a total of 21 index cases. Next-generation sequencing was performed on a predesigned panel of 168 genes associated with heart disease and sudden death. The sequencing analysis revealed twelve (57%) pathogenic or probably pathogenic variants, 9 of them were familial cases, managing to identify pathogenic variants in relatives without symptoms of the disease. At the molecular level, nine of the 12 variants (75%) were single nucleotide changes, 2 (17%) deletions, and 1 (8%) splice site alteration. The genes involved were MYH7 (25%), MYBPC3 (25%) and ACADVL, KCNE1, TNNI3, TPM1, SLC22A5, TNNT2 (8%). In conclusion; we found five variants that were not previously reported in public databases. It is important to follow up on the reclassification of variants, especially those of uncertain significance in patients with symptoms of the condition. All patients included in the study and their relatives received family genetic counseling. Springer Berlin Heidelberg 2023-07-27 2023 /pmc/articles/PMC10657276/ /pubmed/37498360 http://dx.doi.org/10.1007/s00438-023-02048-8 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article García-Vielma, Catalina Lazalde-Córdova, Luis Gerardo Arzola-Hernández, José Cruz González-Aceves, Erick Noel López-Zertuche, Herminio Guzmán-Delgado, Nancy Elena González-Salazar, Francisco Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients |
title | Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients |
title_full | Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients |
title_fullStr | Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients |
title_full_unstemmed | Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients |
title_short | Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients |
title_sort | identification of variants in genes associated with hypertrophic cardiomyopathy in mexican patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657276/ https://www.ncbi.nlm.nih.gov/pubmed/37498360 http://dx.doi.org/10.1007/s00438-023-02048-8 |
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