Maurer, C;
Boleti, O;
Najarzadeh Torbati, P;
Norouzi, F;
Fowler, ANR;
Minaee, S;
Salih, KH;
Taherpour, M;
Birjandi, H;
Alizadeh, B;
et al.
Maurer, C; Boleti, O; Najarzadeh Torbati, P; Norouzi, F; Fowler, ANR; Minaee, S; Salih, KH; Taherpour, M; Birjandi, H; Alizadeh, B; Salih, AF; Bijari, M; Houlden, H; Pittman, AM; Maroofian, R; Almashham, YH; Karimiani, EG; Kaski, JP; Faqeih, EA; Vakilian, F; Jamshidi, Y
(2023)
Genetic Insights from Consanguineous Cardiomyopathy Families.
Genes (Basel), 14 (1).
ISSN 2073-4425
https://doi.org/10.3390/genes14010182
SGUL Authors: Jamshidi, Yalda
Abstract
Inherited cardiomyopathies are a prevalent cause of heart failure and sudden cardiac death. Both hypertrophic (HCM) and dilated cardiomyopathy (DCM) are genetically heterogeneous and typically present with an autosomal dominant mode of transmission. Whole exome sequencing and autozygosity mapping was carried out in eight un-related probands from consanguineous Middle Eastern families presenting with HCM/DCM followed by bioinformatic and co-segregation analysis to predict the potential pathogenicity of candidate variants. We identified homozygous missense variants in TNNI3K, DSP, and RBCK1 linked with a dilated phenotype, in NRAP linked with a mixed phenotype of dilated/hypertrophic, and in KLHL24 linked with a mixed phenotype of dilated/hypertrophic and non-compaction features. Co-segregation analysis in family members confirmed autosomal recessive inheritance presenting in early childhood/early adulthood. Our findings add to the mutational spectrum of recessive cardiomyopathies, supporting inclusion of KLHL24, NRAP and RBCK1 as disease-causing genes. We also provide evidence for novel (recessive) modes of inheritance of a well-established gene TNNI3K and expand our knowledge of the clinical heterogeneity of cardiomyopathies. A greater understanding of the genetic causes of recessive cardiomyopathies has major implications for diagnosis and screening, particularly in underrepresented populations, such as those of the Middle East.
Item Type: |
Article
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Additional Information: |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
Keywords: |
cardiomyopathy, consanguinity, dilated cardiomyopathy (DCM), genetic mutations, hypertrophic cardiomyopathy (HCM), pathogenic variants, whole exome sequencing, Child, Preschool, Humans, Consanguinity, Cardiomyopathies, Cardiomyopathy, Dilated, Mutation, Mutation, Missense, Protein Serine-Threonine Kinases, Humans, Cardiomyopathy, Dilated, Cardiomyopathies, Consanguinity, Mutation, Mutation, Missense, Child, Preschool, Protein Serine-Threonine Kinases, 0604 Genetics |
SGUL Research Institute / Research Centre: |
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) |
Journal or Publication Title: |
Genes (Basel) |
ISSN: |
2073-4425 |
Language: |
eng |
Dates: |
Date | Event |
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10 January 2023 | Published | 7 January 2023 | Accepted |
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Publisher License: |
Creative Commons: Attribution 4.0 |
Projects: |
Project ID | Funder | Funder ID |
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019-052 | KFMC-Research Centre | UNSPECIFIED |
|
PubMed ID: |
36672924 |
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Go to PubMed abstract |
URI: |
https://openaccess.sgul.ac.uk/id/eprint/115158 |
Publisher's version: |
https://doi.org/10.3390/genes14010182 |
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