Genetic interpretation of rare variants associated with arrhythmogenic cardiomyopathy (ACM) is essential due to their diagnostic implications. New data may relabel previous variant classifications, but how often reanalysis is necessary remains undefined. Five years ago, 39 rare ACM-related variants were identified in patients with features of cardiomyopathy. These variants were classified following the American College of Medical Genetics and Genomics’ guidelines. In the present study, we reevaluated these rare variants including novel available data. All cases carried one rare variant classified as being of ambiguous significance (82.05%) or likely pathogenic (17.95%) in 2016. In our comprehensive reanalysis, the classification of 30.77% of these variants changed, mainly due to updated global frequencies. As in 2016, nowadays most variants were classified as having an uncertain role (64.1%), but the proportion of variants with an uncertain role was significantly decreased (17.95%). The percentage of rare variants classified as potentially del-eterious increased from 17.95% to 23.07%. Moreover, 83.33% of reclassified variants gained cer-tainty. We propose that periodic genetic reanalysis of all rare variants associated with arrhythmo-genic cardiomyopathy should be undertaken at least once every five years. Defining the roles of rare variants may help clinicians obtain a definite diagnosis.

Vallverdu-prats, M., Alcalde, M., Sarquella-brugada, G., Cesar, S., Arbelo, E., Fernandez-falgueras, A., Coll, M., Perez-serra, A., Puigmule, M., Iglesias, A., Fiol, V., Ferrer-costa, C., Olmo, B., Pico, F., Lopez, L., Jorda, P., Garcia-alvarez, A., Llano, C. T., Toro, R., Grassi, S., Oliva, A., Brugada, J., Brugada, R., Campuzano, O., Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later, <<JOURNAL OF PERSONALIZED MEDICINE>>, 2021; 2021 (3): 1-14. [doi:10.3390/jpm11030162] [http://hdl.handle.net/10807/175466]

Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later

S.; Oliva;
2021

Abstract

Genetic interpretation of rare variants associated with arrhythmogenic cardiomyopathy (ACM) is essential due to their diagnostic implications. New data may relabel previous variant classifications, but how often reanalysis is necessary remains undefined. Five years ago, 39 rare ACM-related variants were identified in patients with features of cardiomyopathy. These variants were classified following the American College of Medical Genetics and Genomics’ guidelines. In the present study, we reevaluated these rare variants including novel available data. All cases carried one rare variant classified as being of ambiguous significance (82.05%) or likely pathogenic (17.95%) in 2016. In our comprehensive reanalysis, the classification of 30.77% of these variants changed, mainly due to updated global frequencies. As in 2016, nowadays most variants were classified as having an uncertain role (64.1%), but the proportion of variants with an uncertain role was significantly decreased (17.95%). The percentage of rare variants classified as potentially del-eterious increased from 17.95% to 23.07%. Moreover, 83.33% of reclassified variants gained cer-tainty. We propose that periodic genetic reanalysis of all rare variants associated with arrhythmo-genic cardiomyopathy should be undertaken at least once every five years. Defining the roles of rare variants may help clinicians obtain a definite diagnosis.
Inglese
Vallverdu-prats, M., Alcalde, M., Sarquella-brugada, G., Cesar, S., Arbelo, E., Fernandez-falgueras, A., Coll, M., Perez-serra, A., Puigmule, M., Iglesias, A., Fiol, V., Ferrer-costa, C., Olmo, B., Pico, F., Lopez, L., Jorda, P., Garcia-alvarez, A., Llano, C. T., Toro, R., Grassi, S., Oliva, A., Brugada, J., Brugada, R., Campuzano, O., Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later, <<JOURNAL OF PERSONALIZED MEDICINE>>, 2021; 2021 (3): 1-14. [doi:10.3390/jpm11030162] [http://hdl.handle.net/10807/175466]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/175466
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