Cargando…
Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation
BACKGROUND: Mutations of α‐actin gene (ACTC1) have been phenotypically related to various cardiac anomalies, including hypertrophic cardiomyopathy and dilated cardiomyopathy and left ventricular (LV) myocardial noncompaction. A novel ACTC mutation is reported as cosegregating for familial hypertroph...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850207/ https://www.ncbi.nlm.nih.gov/pubmed/29440008 http://dx.doi.org/10.1161/JAHA.117.008068 |
_version_ | 1783306191041986560 |
---|---|
author | Frustaci, Andrea De Luca, Alessandro Guida, Valentina Biagini, Tommaso Mazza, Tommaso Gaudio, Carlo Letizia, Claudio Russo, Matteo Antonio Galea, Nicola Chimenti, Cristina |
author_facet | Frustaci, Andrea De Luca, Alessandro Guida, Valentina Biagini, Tommaso Mazza, Tommaso Gaudio, Carlo Letizia, Claudio Russo, Matteo Antonio Galea, Nicola Chimenti, Cristina |
author_sort | Frustaci, Andrea |
collection | PubMed |
description | BACKGROUND: Mutations of α‐actin gene (ACTC1) have been phenotypically related to various cardiac anomalies, including hypertrophic cardiomyopathy and dilated cardiomyopathy and left ventricular (LV) myocardial noncompaction. A novel ACTC mutation is reported as cosegregating for familial hypertrophic cardiomyopathy and LV myocardial noncompaction with transmural crypts. METHODS AND RESULTS: In an Italian family of 7 subjects, 4 aged 10 (II‐1), 14 (II‐2), 43 (I‐4) and 46 years (I‐5), presenting abnormal ECG changes, dyspnea and palpitation (II‐2, I‐4, and I‐5), and recurrent cerebral ischemic attack (I‐5), underwent 2‐dimensional echo, cardiac magnetic resonance, Holter monitoring, and next‐generation sequencing gene analysis. Patients II‐2 and I‐5 with ventricular tachycardia underwent a cardiac invasive study, including coronary with LV angiography and endomyocardial biopsy. In all the affected members, ECG showed right bundle branch block and left anterior hemiblock with age‐related prolongation of QRS duration. Two‐dimensional echo and cardiac magnetic resonance documented LV myocardial noncompaction in all and in I‐4, I‐5, and II‐2 a progressive LV hypertrophy up to 22‐mm maximal wall thickness. Coronary arteries were normal. LV angiography showed transmural crypts progressing to spongeous myocardial transformation with LV dilatation and dysfunction in the oldest subject. At histology and electron microscopy detachment of myocardiocytes were associated with cell and myofibrillar disarray and degradation of intercalated discs causing disanchorage of myofilaments to cell membrane. Next‐generation sequencing showed in affected members an unreported p.(Ala21Val) mutation of ACTC. CONCLUSIONS: Novel p.(Ala21Val) mutation of ACTC1 causes myofibrillar and intercalated disc alteration leading to familial hypertrophic cardiomyopathy and LV myocardial noncompaction with transmural crypts. |
format | Online Article Text |
id | pubmed-5850207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58502072018-03-21 Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation Frustaci, Andrea De Luca, Alessandro Guida, Valentina Biagini, Tommaso Mazza, Tommaso Gaudio, Carlo Letizia, Claudio Russo, Matteo Antonio Galea, Nicola Chimenti, Cristina J Am Heart Assoc Original Research BACKGROUND: Mutations of α‐actin gene (ACTC1) have been phenotypically related to various cardiac anomalies, including hypertrophic cardiomyopathy and dilated cardiomyopathy and left ventricular (LV) myocardial noncompaction. A novel ACTC mutation is reported as cosegregating for familial hypertrophic cardiomyopathy and LV myocardial noncompaction with transmural crypts. METHODS AND RESULTS: In an Italian family of 7 subjects, 4 aged 10 (II‐1), 14 (II‐2), 43 (I‐4) and 46 years (I‐5), presenting abnormal ECG changes, dyspnea and palpitation (II‐2, I‐4, and I‐5), and recurrent cerebral ischemic attack (I‐5), underwent 2‐dimensional echo, cardiac magnetic resonance, Holter monitoring, and next‐generation sequencing gene analysis. Patients II‐2 and I‐5 with ventricular tachycardia underwent a cardiac invasive study, including coronary with LV angiography and endomyocardial biopsy. In all the affected members, ECG showed right bundle branch block and left anterior hemiblock with age‐related prolongation of QRS duration. Two‐dimensional echo and cardiac magnetic resonance documented LV myocardial noncompaction in all and in I‐4, I‐5, and II‐2 a progressive LV hypertrophy up to 22‐mm maximal wall thickness. Coronary arteries were normal. LV angiography showed transmural crypts progressing to spongeous myocardial transformation with LV dilatation and dysfunction in the oldest subject. At histology and electron microscopy detachment of myocardiocytes were associated with cell and myofibrillar disarray and degradation of intercalated discs causing disanchorage of myofilaments to cell membrane. Next‐generation sequencing showed in affected members an unreported p.(Ala21Val) mutation of ACTC. CONCLUSIONS: Novel p.(Ala21Val) mutation of ACTC1 causes myofibrillar and intercalated disc alteration leading to familial hypertrophic cardiomyopathy and LV myocardial noncompaction with transmural crypts. John Wiley and Sons Inc. 2018-02-10 /pmc/articles/PMC5850207/ /pubmed/29440008 http://dx.doi.org/10.1161/JAHA.117.008068 Text en © 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Frustaci, Andrea De Luca, Alessandro Guida, Valentina Biagini, Tommaso Mazza, Tommaso Gaudio, Carlo Letizia, Claudio Russo, Matteo Antonio Galea, Nicola Chimenti, Cristina Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation |
title | Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation |
title_full | Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation |
title_fullStr | Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation |
title_full_unstemmed | Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation |
title_short | Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation |
title_sort | novel α‐actin gene mutation p.(ala21val) causing familial hypertrophic cardiomyopathy, myocardial noncompaction, and transmural crypts. clinical‐pathologic correlation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850207/ https://www.ncbi.nlm.nih.gov/pubmed/29440008 http://dx.doi.org/10.1161/JAHA.117.008068 |
work_keys_str_mv | AT frustaciandrea novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT delucaalessandro novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT guidavalentina novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT biaginitommaso novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT mazzatommaso novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT gaudiocarlo novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT letiziaclaudio novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT russomatteoantonio novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT galeanicola novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation AT chimenticristina novelaactingenemutationpala21valcausingfamilialhypertrophiccardiomyopathymyocardialnoncompactionandtransmuralcryptsclinicalpathologiccorrelation |