Skip to search boxSkip to navigationSkip to main content

Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients

  • Catalina García-Vielma(corresponding author)
    ,
  • Luis Gerardo Lazalde-Córdova
    ,
  • José Cruz Arzola-Hernández
    ,
  • Erick Noel González-Aceves
    ,
  • Herminio López-Zertuche
    ,
  • Nancy Elena Guzmán-Delgado(corresponding author)
*Corresponding author for this work
  • Instituto Mexicano del Seguro Social
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication metrics

Metrics

SciVal
FWCI
0.30
SciVal
Author count
7
SciVal
Paper percentile
40
SciVal
Citations
4
Scopus
Citations

Abstract

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.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 1289-1299 (11 pages)

Journal (Volume, Issue Number)

Zeitschrift für Induktive Abstammungs- und Vererbungslehre (Volume 298, Issue 6)

Publication milestones

  • Accepted/In press - 2023
  • Published - 11/2023

Publication status

Published - 11/2023

ISSN

1617-4615

Publication IDs

  • Scopus: 85165933359
  • PubMed: 37498360