Genetic Testing for Cardiomyopathies in Clinical Practice

被引:14
|
作者
Ingles, Jodie [1 ,2 ,3 ]
Bagnall, Richard D. [1 ,2 ]
Semsarian, Christopher [1 ,2 ,3 ]
机构
[1] Centenary Inst, Agnes Ginges Ctr Mol Cardiol, Sydney, NSW, Australia
[2] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[3] Royal Prince Alfred Hosp, Dept Cardiol, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Hypertrophic cardiomyopathy; Dilated cardiomyopathy; Arrhythmogenic right ventricular cardiomyopathy; Genetic testing; Genetic counseling; SUDDEN CARDIAC DEATH; INHERITED CARDIOVASCULAR-DISEASES; COST-EFFECTIVENESS MODEL; HYPERTROPHIC CARDIOMYOPATHY; DILATED CARDIOMYOPATHY; UNRELATED PATIENTS; NOONAN SYNDROME; DANON DISEASE; YOUNG-ADULTS; VARIANTS;
D O I
10.1016/j.hfc.2017.12.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac genetic testing for inherited cardiomyopathies has become a routine aspect of care. Advances in genetic testing technologies have made testing more comprehensive and affordable. With this increase comes greater understanding of the genetic basis of these diseases, but also shines a light on the challenges. Ability to ascertain whether a rare variant is causative of disease is problematic. A genetic diagnosis in a family can offer an invaluable tool for cascade genetic testing of at-risk relatives and avenues for reproductive testing options. A careful approach to cardiac genetic testing that recognizes where there is potential for harm ensures the best possible outcomes for families.
引用
收藏
页码:129 / 137
页数:9
相关论文
共 50 条
  • [41] HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
    Ackerman, Michael J.
    Priori, Silvia G.
    Willems, Stephan
    Berul, Charles
    Brugada, Ramon
    Calkins, Hugh
    Camm, A. John
    Ellinor, Patrick T.
    Gollob, Michael
    Hamilton, Robert
    Hershberger, Ray E.
    Judge, Daniel P.
    Le Marec, Herve
    McKenna, William J.
    Schulze-Bahr, Eric
    Semsarian, Chris
    Towbin, Jeffrey A.
    Watkins, Hugh
    Wilde, Arthur
    Wolpert, Christian
    Zipes, Douglas P.
    EUROPACE, 2011, 13 (08): : 1077 - 1109
  • [42] HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
    Ackerman, Michael J.
    Priori, Silvia G.
    Willems, Stephan
    Berul, Charles
    Brugada, Ramon
    Calkins, Hugh
    Camm, A. John
    Ellinor, Patrick T.
    Gollob, Michael
    Hamilton, Robert
    Hershberger, Ray E.
    Judge, Daniel P.
    Le Marec, Herve
    McKenna, William J.
    Schulze-Bahr, Eric
    Semsarian, Chris
    Towbin, Jeffrey A.
    Watkins, Hugh
    Wilde, Arthur
    Wolpert, Christian
    Zipes, Douglas P.
    HEART RHYTHM, 2011, 8 (08) : 1308 - 1339
  • [43] Translation of New and Emerging Therapies for Genetic Cardiomyopathies
    Helms, Adam S.
    Thompson, Andrea D.
    Day, Sharlene M.
    JACC-BASIC TO TRANSLATIONAL SCIENCE, 2022, 7 (01): : 70 - 83
  • [44] Genetic Cardiomyopathies: The Lesson Learned from hiPSCs
    My, Ilaria
    Di Pasquale, Elisa
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (05) : 1 - 24
  • [45] Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies
    Yotti, Raquel
    Seidman, Christine E.
    Seidman, Jonathan G.
    ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 20, 2019, 2019, 20 : 129 - 153
  • [46] Is there a common genetic basis for all familial cardiomyopathies?
    Perrot, Andreas
    Dietz, Rainer
    Osterziel, Karl Josef
    EUROPEAN JOURNAL OF HEART FAILURE, 2007, 9 (01) : 4 - 6
  • [47] Indications and utility of cardiac genetic testing in athletes
    Castelletti, Silvia
    Gray, Belinda
    Basso, Cristina
    Behr, Elijah R.
    Crotti, Lia
    Elliott, Perry M.
    Gonzalez Corcia, Cecilia M.
    D'Ascenzi, Flavio
    Ingles, Jodie
    Loeys, Bart
    Pantazis, Antonis
    Pieles, Guido E.
    Saenen, Johan
    Brugada, Georgia Sarquella
    de la Garza, Maria Sanz
    Sharma, Sanjay
    Van Craenebroek, Emeline M.
    Wilde, Arthur
    Papadakis, Michael
    EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY, 2022, 29 (12) : 1582 - 1591
  • [48] Genetic Testing of Cardiomyopathies: an Update for the Clinician
    Trenkwalde, Teresa
    Knoll, Katharina
    Schunkert, Heribert
    AKTUELLE KARDIOLOGIE, 2024, 13 (03) : 196 - 202
  • [49] Interpretation of Incidental Genetic Findings Localizing to Genes Associated With Cardiac Channelopathies and Cardiomyopathies
    Ezekian, Jordan E.
    Rehder, Catherine
    Kishnani, Priya S.
    Landstrom, Andrew P.
    CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2021, 14 (04): : 535 - 546
  • [50] Genetic Test for Dilated and Hypertrophic Cardiomyopathies: Useful or Less Than Useful for Patients?
    Pastore, F.
    Parisi, V
    Romano, R.
    Rengo, G.
    Pagano, G.
    Komici, K.
    Leosco, D.
    TRANSLATIONAL MEDICINE AT UNISA, 2013, 5 : 14 - 17