Literature DB >> 34384235

Interpretation of Incidental Genetic Findings Localizing to Genes Associated With Cardiac Channelopathies and Cardiomyopathies.

Jordan E Ezekian1, Catherine Rehder2, Priya S Kishnani3, Andrew P Landstrom1,4.   

Abstract

Recent advances in next-genetic sequencing technology have facilitated an expansion in the use of exome and genome sequencing in the research and clinical settings. While this has aided in the genetic diagnosis of individuals with atypical clinical presentations, there has been a marked increase in the number of incidentally identified variants of uncertain diagnostic significance in genes identified as clinically actionable by the American College of Medical Genetics guidelines. Approximately 20 of these genes are associated with cardiac diseases, which carry a significant risk of sudden cardiac death. While identification of at-risk individuals is paramount, increased discovery of incidental variants of uncertain diagnostic significance has placed a burden on the clinician tasked with determining the diagnostic significance of these findings. Herein, we describe the scope of this emerging problem using cardiovascular genetics to illustrate the challenges associated with variants of uncertain diagnostic significance interpretation. We review the evidence for diagnostic weight of these variants, discuss the role of clinical genetics providers in patient care, and put forward general recommendations about the interpretation of incidentally identified variants found with clinical genetic testing.

Entities:  

Keywords:  cardiomyopathies; channelopathies; death, sudden, cardiac; genetic testing; patient care

Mesh:

Year:  2021        PMID: 34384235      PMCID: PMC8375606          DOI: 10.1161/CIRCGEN.120.003200

Source DB:  PubMed          Journal:  Circ Genom Precis Med        ISSN: 2574-8300


  97 in total

1.  Variability in assigning pathogenicity to incidental findings: insights from LDLR sequence linked to the electronic health record in 1013 individuals.

Authors:  Maya S Safarova; Eric W Klee; Linnea M Baudhuin; Erin M Winkler; Michelle L Kluge; Suzette J Bielinski; Janet E Olson; Iftikhar J Kullo
Journal:  Eur J Hum Genet       Date:  2017-02-01       Impact factor: 4.246

2.  Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.

Authors:  Ferhaan Ahmad; Elizabeth M McNally; Michael J Ackerman; Linda C Baty; Sharlene M Day; Iftikhar J Kullo; Peace C Madueme; Martin S Maron; Matthew W Martinez; Lisa Salberg; Matthew R Taylor; Janel E Wilcox
Journal:  Circ Genom Precis Med       Date:  2019-05-23

Review 3.  What can exome sequencing do for you?

Authors:  Jacek Majewski; Jeremy Schwartzentruber; Emilie Lalonde; Alexandre Montpetit; Nada Jabado
Journal:  J Med Genet       Date:  2011-07-05       Impact factor: 6.318

Review 4.  Arrhythmogenic right ventricular cardiomyopathy: perspectives on disease.

Authors:  M W Norman; W J McKenna
Journal:  Z Kardiol       Date:  1999-08

5.  Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.

Authors:  Sara L Van Driest; Quinn S Wells; Sarah Stallings; William S Bush; Adam Gordon; Deborah A Nickerson; Jerry H Kim; David R Crosslin; Gail P Jarvik; David S Carrell; James D Ralston; Eric B Larson; Suzette J Bielinski; Janet E Olson; Zi Ye; Iftikhar J Kullo; Noura S Abul-Husn; Stuart A Scott; Erwin Bottinger; Berta Almoguera; John Connolly; Rosetta Chiavacci; Hakon Hakonarson; Laura J Rasmussen-Torvik; Vivian Pan; Stephen D Persell; Maureen Smith; Rex L Chisholm; Terrie E Kitchner; Max M He; Murray H Brilliant; John R Wallace; Kimberly F Doheny; M Benjamin Shoemaker; Rongling Li; Teri A Manolio; Thomas E Callis; Daniela Macaya; Marc S Williams; David Carey; Jamie D Kapplinger; Michael J Ackerman; Marylyn D Ritchie; Joshua C Denny; Dan M Roden
Journal:  JAMA       Date:  2016-01-05       Impact factor: 56.272

6.  Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.

Authors:  Sarah S Kalia; Kathy Adelman; Sherri J Bale; Wendy K Chung; Christine Eng; James P Evans; Gail E Herman; Sophia B Hufnagel; Teri E Klein; Bruce R Korf; Kent D McKelvey; Kelly E Ormond; C Sue Richards; Christopher N Vlangos; Michael Watson; Christa L Martin; David T Miller
Journal:  Genet Med       Date:  2016-11-17       Impact factor: 8.822

7.  Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy.

Authors:  Pamela A Long; Jared M Evans; Timothy M Olson
Journal:  J Cardiovasc Dev Dis       Date:  2017-08-08

8.  Clinical sequencing: is WGS the better WES?

Authors:  Janine Meienberg; Rémy Bruggmann; Konrad Oexle; Gabor Matyas
Journal:  Hum Genet       Date:  2016-01-07       Impact factor: 4.132

9.  Natural History of Dilated Cardiomyopathy in Children.

Authors:  Ilaria Puggia; Marco Merlo; Giulia Barbati; Teisha J Rowland; Davide Stolfo; Marta Gigli; Federica Ramani; Andrea Di Lenarda; Luisa Mestroni; Gianfranco Sinagra
Journal:  J Am Heart Assoc       Date:  2016-06-30       Impact factor: 5.501

10.  Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes.

Authors:  Isabel Diebold; Ulrike Schön; Florentine Scharf; Anna Benet-Pagès; Andreas Laner; Elke Holinski-Feder; Angela Abicht
Journal:  Hum Mutat       Date:  2020-02-18       Impact factor: 4.878

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  1 in total

1.  Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy.

Authors:  Leonie M Kurzlechner; Edward G Jones; Amy M Berkman; Hanna J Tadros; Jill A Rosenfeld; Yaping Yang; Hari Tunuguntla; Hugh D Allen; Jeffrey J Kim; Andrew P Landstrom
Journal:  J Pers Med       Date:  2022-04-30
  1 in total

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