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Erschienen in: Journal of Cardiovascular Translational Research 6/2023

29.11.2023 | Review

The Trouble with Trabeculation: How Genetics Can Help to Unravel a Complex and Controversial Phenotype

verfasst von: Roddy Walsh

Erschienen in: Journal of Cardiovascular Translational Research | Ausgabe 6/2023

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Abstract

Excessive trabeculation of the cardiac left ventricular wall is a complex phenotypic substrate associated with various physiological and pathological processes. There has been considerable conjecture as to whether hypertrabeculation contributes to disease and whether left ventricular non-compaction (LVNC) cardiomyopathy is a distinct pathology. Building on recent insights into the genetic basis of LVNC cardiomyopathy, in particular three meta-analysis studies exploring genotype–phenotype associations using different methodologies, this review examines how genetic research can advance our understanding of trabeculation. Three groups of genes implicated in LVNC are described—those associated with other cardiomyopathies, other cardiac/syndromic conditions and putatively with isolated LVNC cardiomyopathy—demonstrating how these findings can inform the underlying pathologies in LVNC patients and aid differential diagnosis and management in clinical practice despite the limited utility suggested for LVNC genetic testing in recent guidelines. The outstanding questions and future research priorities for exploring the genetics of hypertrabeculation are discussed.

Graphical Abstract

Literatur
1.
Zurück zum Zitat Maron BJ, Towbin JA, Thiene G, Antzelevitch C, Corrado D, Arnett D, Council on Epidemiology and Prevention. Contemporary Definitions and Classification of the Cardiomyopathies: an American Heart Association Scientific Statement From the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation. 2006;113(14):1807–16. https://doi.org/10.1161/CIRCULATIONAHA.106.174287.CrossRefPubMed Maron BJ, Towbin JA, Thiene G, Antzelevitch C, Corrado D, Arnett D, Council on Epidemiology and Prevention. Contemporary Definitions and Classification of the Cardiomyopathies: an American Heart Association Scientific Statement From the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation. 2006;113(14):1807–16. https://​doi.​org/​10.​1161/​CIRCULATIONAHA.​106.​174287.CrossRefPubMed
2.
Zurück zum Zitat Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, … Keren A. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J 2008;29(2): 270–6. https://doi.org/10.1093/eurheartj/ehm342. Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, … Keren A. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J 2008;29(2): 270–6. https://​doi.​org/​10.​1093/​eurheartj/​ehm342.​
5.
Zurück zum Zitat Gati S, Chandra N, Bennett RL, Reed M, Kervio G, Panoulas VF, … Sharma S. Increased left ventricular trabeculation in highly trained athletes: do we need more stringent criteria for the diagnosis of left ventricular non-compaction in athletes? Heart (British Cardiac Society) 2013;99(6):401–8. https://doi.org/10.1136/heartjnl-2012-303418. Gati S, Chandra N, Bennett RL, Reed M, Kervio G, Panoulas VF, … Sharma S. Increased left ventricular trabeculation in highly trained athletes: do we need more stringent criteria for the diagnosis of left ventricular non-compaction in athletes? Heart (British Cardiac Society) 2013;99(6):401–8. https://​doi.​org/​10.​1136/​heartjnl-2012-303418.​
7.
12.
16.
Zurück zum Zitat Richard P, Ader F, Roux M, Donal E, Eicher J-C, Aoutil N, … Charron P. Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity. Clin Genet 2019;95(3):356–367. https://doi.org/10.1111/cge.13484. Richard P, Ader F, Roux M, Donal E, Eicher J-C, Aoutil N, … Charron P. Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity. Clin Genet 2019;95(3):356–367. https://​doi.​org/​10.​1111/​cge.​13484.​
18.
22.
Zurück zum Zitat Walsh R, Mazzarotto F, Whiffin N, Buchan R, Midwinter W, Wilk A, … Ware JS. Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy. Genome Med 2019;11(1):5. https://doi.org/10.1186/s13073-019-0616-z. Walsh R, Mazzarotto F, Whiffin N, Buchan R, Midwinter W, Wilk A, … Ware JS. Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy. Genome Med 2019;11(1):5. https://​doi.​org/​10.​1186/​s13073-019-0616-z.​
23.
Zurück zum Zitat Lehman SJ, Meller A, Solieva SO, Lotthammer JM, Greenberg L, Langer SJ, … Leinwand L. Divergent molecular phenotypes in point mutations at the same residue in beta-myosin heavy chain lead to distinct cardiomyopathies. bioRxiv : the preprint server for biology. 2023;https://doi.org/10.1101/2023.07.03.547580. Lehman SJ, Meller A, Solieva SO, Lotthammer JM, Greenberg L, Langer SJ, … Leinwand L. Divergent molecular phenotypes in point mutations at the same residue in beta-myosin heavy chain lead to distinct cardiomyopathies. bioRxiv : the preprint server for biology. 2023;https://​doi.​org/​10.​1101/​2023.​07.​03.​547580.​
27.
32.
36.
Zurück zum Zitat Kodo K, Ong S-G, Jahanbani F, Termglinchan V, Hirono K, InanlooRahatloo K, … Wu JC. iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy. Nat Cell Biol 2016;18(10):1031–42. https://doi.org/10.1038/ncb3411. Kodo K, Ong S-G, Jahanbani F, Termglinchan V, Hirono K, InanlooRahatloo K, … Wu JC. iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy. Nat Cell Biol 2016;18(10):1031–42. https://​doi.​org/​10.​1038/​ncb3411.​
38.
Zurück zum Zitat Myasnikov R, Brodehl A, Meshkov A, Kulikova O, Kiseleva A, Pohl GM, … Drapkina O. The double mutation DSG2-p.S363X and TBX20-p.D278X is associated with left ventricular non-compaction cardiomyopathy: case report. Int J Mol Sci 2021;22(13). https://doi.org/10.3390/ijms22136775. Myasnikov R, Brodehl A, Meshkov A, Kulikova O, Kiseleva A, Pohl GM, … Drapkina O. The double mutation DSG2-p.S363X and TBX20-p.D278X is associated with left ventricular non-compaction cardiomyopathy: case report. Int J Mol Sci 2021;22(13). https://​doi.​org/​10.​3390/​ijms22136775.​
40.
Zurück zum Zitat Chang Y, Wacker J, Ingles J, Macciocca I, King I. Australian Genomics Cardiovascular Disorders Flagship, … Bagnall RD. TBX20 loss-of-function variants in families with left ventricular non-compaction cardiomyopathy. J Med Genet 2023;https://doi.org/10.1136/jmg-2023-109455. Chang Y, Wacker J, Ingles J, Macciocca I, King I. Australian Genomics Cardiovascular Disorders Flagship, … Bagnall RD. TBX20 loss-of-function variants in families with left ventricular non-compaction cardiomyopathy. J Med Genet 2023;https://​doi.​org/​10.​1136/​jmg-2023-109455.​
41.
Zurück zum Zitat Luxán G, Casanova JC, Martínez-Poveda B, Prados B, D’Amato G, MacGrogan D, … de la Pompa JL. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy. Nat Med 2013;19(2):193–201. https://doi.org/10.1038/nm.3046. Luxán G, Casanova JC, Martínez-Poveda B, Prados B, D’Amato G, MacGrogan D, … de la Pompa JL. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy. Nat Med 2013;19(2):193–201. https://​doi.​org/​10.​1038/​nm.​3046.​
43.
Zurück zum Zitat Wilde AAM, Semsarian C, Márquez MF, Shamloo AS, Ackerman MJ, Ashley EA, … Developed in partnership with and endorsed by the European Heart Rhythm Association (EHRA), a branch of the European Society of Cardiology (ESC), the Heart Rhythm Society (HRS), the Asia Pacific Heart Rhythm Society (APHRS), and the L. A. H. R. S. (LAHRS). European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022;24(8):1307–1367. https://doi.org/10.1093/europace/euac030. Wilde AAM, Semsarian C, Márquez MF, Shamloo AS, Ackerman MJ, Ashley EA, … Developed in partnership with and endorsed by the European Heart Rhythm Association (EHRA), a branch of the European Society of Cardiology (ESC), the Heart Rhythm Society (HRS), the Asia Pacific Heart Rhythm Society (APHRS), and the L. A. H. R. S. (LAHRS). European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022;24(8):1307–1367. https://​doi.​org/​10.​1093/​europace/​euac030.
47.
Zurück zum Zitat Myasnikov RP, Kulikova OV, Meshkov AN, Bukaeva AA, Kiseleva AV, Ershova AI, … Drapkina OM. A splice variant of the MYH7 gene is causative in a family with isolated left ventricular noncompaction cardiomyopathy. Genes 2022;13(10). https://doi.org/10.3390/genes13101750. Myasnikov RP, Kulikova OV, Meshkov AN, Bukaeva AA, Kiseleva AV, Ershova AI, … Drapkina OM. A splice variant of the MYH7 gene is causative in a family with isolated left ventricular noncompaction cardiomyopathy. Genes 2022;13(10). https://​doi.​org/​10.​3390/​genes13101750.​
51.
Zurück zum Zitat Piekutowska-Abramczuk D, Paszkowska A, Ciara E, Frączak K, Mirecka-Rola A, Wicher D, … Ziółkowska L. Genetic profile of left ventricular noncompaction cardiomyopathy in children-a single reference center experience. Genes 2022;13(8). https://doi.org/10.3390/genes13081334. Piekutowska-Abramczuk D, Paszkowska A, Ciara E, Frączak K, Mirecka-Rola A, Wicher D, … Ziółkowska L. Genetic profile of left ventricular noncompaction cardiomyopathy in children-a single reference center experience. Genes 2022;13(8). https://​doi.​org/​10.​3390/​genes13081334.​
54.
Zurück zum Zitat Schultze-Berndt A, Kühnisch J, Herbst C, Seidel F, Al-Wakeel-Marquard N, Dartsch J, … Klaassen S. Reduced Systolic function and not genetic variants determine outcome in pediatric and adult left ventricular noncompaction cardiomyopathy. Front Pediatr 2021;9:722926. https://doi.org/10.3389/fped.2021.722926. Schultze-Berndt A, Kühnisch J, Herbst C, Seidel F, Al-Wakeel-Marquard N, Dartsch J, … Klaassen S. Reduced Systolic function and not genetic variants determine outcome in pediatric and adult left ventricular noncompaction cardiomyopathy. Front Pediatr 2021;9:722926. https://​doi.​org/​10.​3389/​fped.​2021.​722926.​
55.
56.
Zurück zum Zitat Singer ES, Ross SB, Skinner JR, Weintraub RG, Ingles J, Semsarian C, Bagnall RD. Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death. Gen Med: official journal of the American College of Medical Genetics. 2021;23(1):86–93. https://doi.org/10.1038/s41436-020-00970-5.CrossRef Singer ES, Ross SB, Skinner JR, Weintraub RG, Ingles J, Semsarian C, Bagnall RD. Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death. Gen Med: official journal of the American College of Medical Genetics. 2021;23(1):86–93. https://​doi.​org/​10.​1038/​s41436-020-00970-5.CrossRef
57.
58.
Zurück zum Zitat Delplancq G, Tarris G, Vitobello A, Nambot S, Sorlin A, Philippe C, … Kuentz P. Cardiomyopathy due to PRDM16 mutation: first description of a fetal presentation, with possible modifier genes. Am J Med Genet. Part C, Seminars in medical genetics 2020;https://doi.org/10.1002/ajmg.c.31766. Delplancq G, Tarris G, Vitobello A, Nambot S, Sorlin A, Philippe C, … Kuentz P. Cardiomyopathy due to PRDM16 mutation: first description of a fetal presentation, with possible modifier genes. Am J Med Genet. Part C, Seminars in medical genetics 2020;https://​doi.​org/​10.​1002/​ajmg.​c.​31766.​
60.
Zurück zum Zitat Hirono K, Hata Y, Miyao N, Okabe M, Takarada S, Nakaoka H, … Lvnc Study Collaborators. Left ventricular noncompaction and congenital heart disease increases the risk of congestive heart failure. J Clin Med 2020;9(3). https://doi.org/10.3390/jcm9030785. Hirono K, Hata Y, Miyao N, Okabe M, Takarada S, Nakaoka H, … Lvnc Study Collaborators. Left ventricular noncompaction and congenital heart disease increases the risk of congestive heart failure. J Clin Med 2020;9(3). https://​doi.​org/​10.​3390/​jcm9030785.​
Metadaten
Titel
The Trouble with Trabeculation: How Genetics Can Help to Unravel a Complex and Controversial Phenotype
verfasst von
Roddy Walsh
Publikationsdatum
29.11.2023
Verlag
Springer US
Erschienen in
Journal of Cardiovascular Translational Research / Ausgabe 6/2023
Print ISSN: 1937-5387
Elektronische ISSN: 1937-5395
DOI
https://doi.org/10.1007/s12265-023-10459-6

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