Current Challenges in Cardiovascular Molecular Diagnostics

The field of cardiovascular genetics has tremendously benefited from the recent application of massive parallel sequencing technology also referred to as next generation sequencing (NGS). However, along with the discovery of additional genes associated with human cardiac diseases, the analysis of la...

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Главные авторы: Carlo Napolitano, Jeffrey A. Towbin, Guia Guffanti, Luisa Mestroni, Valeria Novelli, Matteo Vatta
Формат: Online
Язык:английский
Опубликовано: Frontiers Media SA 2021
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author Carlo Napolitano
Jeffrey A. Towbin
Guia Guffanti
Luisa Mestroni
Valeria Novelli
Matteo Vatta
author_browse Carlo Napolitano
Guia Guffanti
Jeffrey A. Towbin
Luisa Mestroni
Matteo Vatta
Valeria Novelli
author_facet Carlo Napolitano
Jeffrey A. Towbin
Guia Guffanti
Luisa Mestroni
Valeria Novelli
Matteo Vatta
author_sort Carlo Napolitano
collection Directory of Open Access Books
description The field of cardiovascular genetics has tremendously benefited from the recent application of massive parallel sequencing technology also referred to as next generation sequencing (NGS). However, along with the discovery of additional genes associated with human cardiac diseases, the analysis of large dataset of genetic information uncovered a much more complex and variegated landscape, which often departs from the comfort zone of the monogenic Mendelian diseases image that clinical molecular geneticists have been well acquainted with for many decades. It is now clear that, in addition to highly penetrant genetic variants, which in isolation are able to recapitulate the full clinical presentation when expressed in animal models, we are now aware that a small but significant fraction of subjects presenting with cardiac muscle diseases such as cardiomyopathies or primary arrhythmias such as long QT syndrome (LQTS), may harbor at least two deleterious variants in the same gene (compound heterozygous) or in different gene (double heterozygous). Although the clinical presentation in subjects with more than one deleterious variant appears to be more severe and with an earlier disease onset, it somehow changes the viewpoint of clinical molecular geneticists whose aim is to identify all possible genetic contributors to a human condition. In this light, the employment in clinical diagnostics of the NGS technology, allowing the simultaneous interrogation of a DNA target spanning from large panel of genes up to the entire genome, will definitely aid at uncovering all such contributors, which will have to be tested functionally to confirm their role in human cardiac conditions. The uncovering of all clinically relevant deleterious changes associated with a cardiovascular disease would probably increase our understanding of the clinical variability commonly occurring among affected family relatives, and potentially provide with unexpected therapeutic targets for the treatment of symptoms related to the presence of “accessory” deleterious genetic variants other than the key molecular culprit. The objective of this Research Topic is to explore the current challenges presenting to the cardiovascular genetics providers, such as clinical geneticists, genetic counselors, clinical molecular geneticists and molecular pathologists involved in the diagnosis, counseling, testing and interpretation of genetic tests results for the comprehensive management of patients affected by cardiovascular genetic disorders.
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spelling doab-20.500.12854ir-444092024-03-30T23:21:40Z Current Challenges in Cardiovascular Molecular Diagnostics Carlo Napolitano Jeffrey A. Towbin Guia Guffanti Luisa Mestroni Valeria Novelli Matteo Vatta R5-920 genetic variants Cardiovascular Diseases Genetic Testing channelopathy variant interpretation NGS Sudden cardiac death cardiomyopathy Cardiovascular genetics thema EDItEUR::M Medicine and Nursing The field of cardiovascular genetics has tremendously benefited from the recent application of massive parallel sequencing technology also referred to as next generation sequencing (NGS). However, along with the discovery of additional genes associated with human cardiac diseases, the analysis of large dataset of genetic information uncovered a much more complex and variegated landscape, which often departs from the comfort zone of the monogenic Mendelian diseases image that clinical molecular geneticists have been well acquainted with for many decades. It is now clear that, in addition to highly penetrant genetic variants, which in isolation are able to recapitulate the full clinical presentation when expressed in animal models, we are now aware that a small but significant fraction of subjects presenting with cardiac muscle diseases such as cardiomyopathies or primary arrhythmias such as long QT syndrome (LQTS), may harbor at least two deleterious variants in the same gene (compound heterozygous) or in different gene (double heterozygous). Although the clinical presentation in subjects with more than one deleterious variant appears to be more severe and with an earlier disease onset, it somehow changes the viewpoint of clinical molecular geneticists whose aim is to identify all possible genetic contributors to a human condition. In this light, the employment in clinical diagnostics of the NGS technology, allowing the simultaneous interrogation of a DNA target spanning from large panel of genes up to the entire genome, will definitely aid at uncovering all such contributors, which will have to be tested functionally to confirm their role in human cardiac conditions. The uncovering of all clinically relevant deleterious changes associated with a cardiovascular disease would probably increase our understanding of the clinical variability commonly occurring among affected family relatives, and potentially provide with unexpected therapeutic targets for the treatment of symptoms related to the presence of “accessory” deleterious genetic variants other than the key molecular culprit. The objective of this Research Topic is to explore the current challenges presenting to the cardiovascular genetics providers, such as clinical geneticists, genetic counselors, clinical molecular geneticists and molecular pathologists involved in the diagnosis, counseling, testing and interpretation of genetic tests results for the comprehensive management of patients affected by cardiovascular genetic disorders. 2021-02-11T10:53:02Z 2021-02-11T10:53:02Z 2018-02-27 16:16:44 2017 book 25590 16648714 9782889452811 https://directory.doabooks.org/handle/20.500.12854/44409 eng Frontiers Research Topics image/jpeg Attribution 4.0 International http://www.frontiersin.org/books/Current_Challenges_in_Cardiovascular_Molecular_Diagnostics/1324#nogo http://journal.frontiersin.org/researchtopic/4244/current-challenges-in-cardiovascular-molecular-diagnostics Frontiers Media SA 10.3389/978-2-88945-281-1 10.3389/978-2-88945-281-1 bf5ce210-e72e-4860-ba9b-c305640ff3ae 9782889452811 128 open access
spellingShingle R5-920
genetic variants
Cardiovascular Diseases
Genetic Testing
channelopathy
variant interpretation
NGS
Sudden cardiac death
cardiomyopathy
Cardiovascular genetics
thema EDItEUR::M Medicine and Nursing
Carlo Napolitano
Jeffrey A. Towbin
Guia Guffanti
Luisa Mestroni
Valeria Novelli
Matteo Vatta
Current Challenges in Cardiovascular Molecular Diagnostics
title Current Challenges in Cardiovascular Molecular Diagnostics
title_full Current Challenges in Cardiovascular Molecular Diagnostics
title_fullStr Current Challenges in Cardiovascular Molecular Diagnostics
title_full_unstemmed Current Challenges in Cardiovascular Molecular Diagnostics
title_short Current Challenges in Cardiovascular Molecular Diagnostics
title_sort current challenges in cardiovascular molecular diagnostics
topic R5-920
genetic variants
Cardiovascular Diseases
Genetic Testing
channelopathy
variant interpretation
NGS
Sudden cardiac death
cardiomyopathy
Cardiovascular genetics
thema EDItEUR::M Medicine and Nursing
topic_facet R5-920
genetic variants
Cardiovascular Diseases
Genetic Testing
channelopathy
variant interpretation
NGS
Sudden cardiac death
cardiomyopathy
Cardiovascular genetics
thema EDItEUR::M Medicine and Nursing
url 25590
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