Sarcomere Mutations in Cardiomyopathy, Noncompaction, and the Developing Heart

Abstract

HomeCirculationVol. 117, No. 22Sarcomere Mutations in Cardiomyopathy, Noncompaction, and the Developing Heart Free AccessEditorialPDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessEditorialPDF/EPUBSarcomere Mutations in Cardiomyopathy, Noncompaction, and the Developing Heart Lisa Dellefave, MS, CGC and Elizabeth M. McNally, MD, PhD Lisa DellefaveLisa Dellefave From the Department of Medicine, Department of Human Genetics, University of Chicago, Chicago, Ill. Search for more papers by this author and Elizabeth M. McNallyElizabeth M. McNally From the Department of Medicine, Department of Human Genetics, University of Chicago, Chicago, Ill. Search for more papers by this author Originally published3 Jun 2008https://doi.org/10.1161/CIRCULATIONAHA.108.781518Circulation. 2008;117:2847–2849In this issue of Circulation, Klaassen and colleagues1 describe mutations in the genes encoding myosin heavy chain (MHC), cardiac actin, and troponin T in patients with left ventricular noncompaction (LVNC). LVNC, defined as excessive and unusual trabeculation of the mature left ventricle, is thought to reflect a developmental failure of the heart to form fully the compact myocardium during the later stages of cardiac development. Previously, mutations in sarcomeric genes have been linked extensively to the development of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM). The finding of similar, but not identical, mutations in patients with LVNC suggests a continuum of cardiomyopathy that includes LVNC and further supports the essential role for normal sarcomere function during cardiac development.Article p 2893Noncompaction of the ventricular myocardium is characterized by a spongy morphological appearance of the myocardium occurring primarily in the left ventricle and most evident in the apical portion.2 Noncompaction often is visualized as deep recesses within the thickened apex, and these sinusoids communicate with the ventricular cavity. During heart development, the myocardium is initially trabeculated during a period before coronary artery development and is thought to be an adaptation to provide blood flow to the developing myocardium. The development of the coronary vasculature is associated temporally with the loss of trabeculae and the full maturation of the compact myocardium. Between embryonic weeks 5 and 8, the trabeculae regress as the compact myocardium develops from base to apex. Isolated LVNC is defined as occurring in the absence of other cardiac structural malformation. Nonsyndromic LVNC refers to the absence of other extracardiac developmental disorders. In 2006, the American Heart Association scientific statement on classification of cardiomyopathies reclassified LVNC as its own disease entity.3Klaassen et al now link genetic sarcomere defects to both familial and sporadic isolated, nonsyndromic LVNC. The authors identified 63 unrelated subjects with echocardiographic criteria for LVNC and notably without HCM or DCM. The cohort was screened for mutations in 6 sarcomere genes: β-MHC (MYH7), troponin T (TNNT2), troponin I (TNNI3), myosin regulatory light chain (MYL2), myosin essential light chain (MYL3), and cardiac α-actin (ACTC). Eleven of 63 subjects (17%) were found to have heterozygous mutations in 3 different sarcomeric genes. Eight of 11 were in MYH7, 2 were in ACTC, and 1 was in TNNT2. Of the 11 individuals identified with sarcomeric gene mutations, 6 had relatives with LVNC, consistent with familial disease. The remaining 5 had sporadic disease, and in 1 individual, neither parent carried the mutation, indicating a de novo mutation. The age range of presentation was 15 to 60 years, and the clinical constellation of symptoms included arrhythmias, heart failure, and embolic events.The LVNC-associated mutations in β-MHC clustered so that 6 of 8 mutations were in exons 8 and 9 of MYH7. Four of these mutations uniquely affected splicing, and the predicted protein product, if made, includes only the first 25-kDa portion of β-MHC, a region that encodes a fragment of the enzymatically active head region. This peptide may be capable of interfering with the actin-myosin interface. Alternatively, it is possible that missplicing effectively results in an absence of protein so that the haploinsufficiency of MYH7 may contribute to the development of LVNC. Many HCM-associated mutations have been described in exons 8 and 9 of MYH7 (http://www.cardiogenomics.org). It is important to determine whether these mutations are more likely to associate with increased trabeculation and potentially an increased embolic risk. Although Klaassen et al describe isolated LVNC associated with the missense mutation MYH7 R243H, this same mutation was previously reported with apical HCM, suggesting an interrelationship between apical HCM and LVNC.4The Klaassen et al study also describes 2 unrelated LVNC cases, both carrying the same cardiac actin (ACTC) gene defect, E101K. The cardiac actin gene was previously implicated in both HCM and DCM and was noted specifically in cardiomyopathy gene mutation carriers with unusual apical thickening and trabeculation.5 The unusual apical disease led Monserrat and colleagues6 to screen 247 index cases with HCM, DCM, or LVNC specifically for the ACTC E101K gene mutation (166 with HCM, 76 with DCM, 5 with LVNC). The same ACTCE101K mutation now found by Klaassen et al was identified in 5 families, all from Galicia, Spain, and consistent with a founder effect. Within the Galician families, there were individuals with apical trabeculation that was independent of apical hypertrophy, as well as individuals meeting criteria for isolated LVNC. Curiously, congenital defects, including ostium secundum, atrial septal defect, and ventricular septal defect, were described in several family members, consistent with the idea that sarcomere gene mutations can produce cardiac developmental anomalies.The Clinical Spectrum From Sarcomeric Gene MutationsSarcomeric gene mutations link to HCM, DCM, and LVNC. As with most monogenetic disease, there is diversity of clinical outcome, only some of which is explained by the precise mutation. Individuals carrying the identical sarcomeric gene mutation display a phenotypic spectrum that may span from those with early-onset, lethal disease to those without evidence of cardiomyopathy. The expressivity of sarcomeric gene mutations in HCM and DCM affects age of onset, age of heart failure symptoms, and importantly, accompanying arrhythmias. Similarly, LVNC sarcomeric gene mutations have a similar broad range of expressivity. As noted by Klaassen et al, the R243H mutation was found in 4 family members meeting LVNC criteria; the 65-year-old grandmother was found to have asymptomatic LVNC, whereas her grandson was diagnosed with LVNC at 2 years of age.1 This finding underscores the need for family screening in LVNC cases.The variables that alter the phenotypic outcome in these disorders are largely unknown but include environmental factors such as diet and exercise7,8 and, importantly, also include many unknown genetic factors. The presence of modifier genes can be associated with protective effects or enhancing effects to mediate a more severe outcome. These genetic modifier loci may fall within genetic pathways similar to the primary genetic defect. For example, the presence of 2 distinct sarcomeric gene mutations occurs rarely but is associated with early-onset severe disease.9,10 Finally, nonsense-mediated decay, a process in which the mutant mRNA is preferentially reduced, may account for considerable variability because effectively the amount of mutant RNA and protein may differ substantially among individuals.The families described by Klaassen et al have isolated LVNC without HCM or DCM. However, it has been established that the genetic spectrum from a single mutation can lead to LVNC or apical HCM within a given family.4 As mentioned, the identical ACTC mutation can associate with LVNC or cardiomyopathy within the same family.6 Similarly, the missense MYH7 mutation L301Q was found in an individual with LVNC and DCM whose family history included DCM and congestive heart failure.11 A second family was identified as having 2 MYH7 missense mutations on the same allele, D545N (exon 16) and D955N (exon 23), resulting in LVNC with DCM-like features. The families reported by Klaassen et al are distinct because they lack HCM and DCM, and this observation may correlate with the high prevalence of splice-site mutations.Diagnostic limitations can influence the designation of LVNC versus HCM or even DCM because echocardiography can be limited in its ability to delineate trabeculations. Additionally, the findings of LVNC, along with HCM or DCM, within the same family need not implicate a sarcomeric gene mutation because a mutation in the nuclear membrane gene, LMNA, has been described in families with both LVNC and DCM.12LMNA encodes the nuclear membrane proteins lamins A and C. A missense mutation, R190W, was identified in a family in which 1 asymptomatic individual had isolated LVNC and 3 others had DCM.12Developmental ImplicationsLVNC may be present at birth, consistent with a developmental defect. Because LVNC often is diagnosed later in life, it is frequently unknown at which stage LVNC developed and whether the morphology progressed with time. Symptomatic LVNC in early life, consistent with congenital disease, is typically more severe, as are many forms of pediatric cardiomyopathy. The diagnosis of LVNC, particularly familial LVNC, should warrant screening of relatives even in early life. The morphology of LVNC mirrors the appearance of the early developing heart. During myocardial maturation, the developing endocardium is deeply trabeculated. Obstruction of outflow during this window of heart development may enhance noncompaction because valvar atretic lesions can enhance noncompaction.2,13 The putative abnormal force generation that may result from sarcomere mutations, particularly MYH7, is consistent with a requirement of normal force production during this developmental window. Supporting the developmental role of MYH7, an R281T mutation was described in a family with LVNC. Intriguingly, 3 individuals also had associated Epstein anomaly and atrial septal defects. This mutation, similar to 6 of the 8 mutations reported by Klaassen et al, falls near the ATPase active site of MHC.14 Therefore, a mechanism that unifies chamber septation and morphological regression of the trabeculated myocardium may be developmentally linked through the sarcomere.ConclusionsThere is substantial evidence to place LVNC in the context of other cardiomyopathies. The Klaassen et al study clearly demarcates the role of sarcomeric gene mutations as accounting for a significant percentage of LVNC. The study further highlights the potential familial nature of LVNC and the need to evaluate family members of LVNC patients. It has been estimated that 44% of LVNC patients have familial disease.2 The reports linking LVNC to other forms of cardiomyopathy indicate that family members should be evaluated not only for HCM or DCM but also for septation defects.The opinions expressed in this article are not necessarily those of the editors or of the American Heart Association.Dr McNally and L. Dellefave are supported by the Doris Duke Charitable Foundation.DisclosuresNone.FootnotesCorrespondence to E.M. McNally, MD, PhD, The University of Chicago, 5841 S. Maryland Ave, MC6088, Chicago, IL 60637. E-mail [email protected] References 1 Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn J-D, Heuser A, Berger F, Jenni R, Thierfelder L. Mutations in sarcomere protein genes in left ventricular noncompaction. Circulation. 2008; 117: 2893–2901.LinkGoogle Scholar2 Engberding R, Yelbuz TM, Breithardt G. Isolated noncompaction of the left ventricular myocardium: a review of the literature two decades after the initial case description. Clin Res Cardiol. 2007; 96: 481–488.CrossrefMedlineGoogle Scholar3 Maron BJ, Towbin JA, Thiene G, Antzelevitch C, Corrado D, Arnett D, Moss AJ, Seidman CE, Young JB. 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: 1807–1816.LinkGoogle Scholar4 Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE. Gene mutations in apical hypertrophic cardiomyopathy. Circulation. 2005; 112: 2805–2811.LinkGoogle Scholar5 Olson TM, Doan TP, Kishimoto NY, Whitby FG, Ackerman MJ, Fananapazir L. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy. J Mol Cell Cardiol. 2000; 32: 1687–1694.CrossrefMedlineGoogle Scholar6 Monserrat L, Hermida-Prieto M, Fernandez X, Rodriguez I, Dumont C, Cazon L, Cuesta MG, Gonzalez-Juanatey C, Peteiro J, Alvarez N, Penas-Lado M, Castro-Beiras A. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects. Eur Heart J. 2007; 28: 1953–1961.CrossrefMedlineGoogle Scholar7 Konhilas JP, Watson PA, Maass A, Boucek DM, Horn T, Stauffer BL, Luckey SW, Rosenberg P, Leinwand LA. Exercise can prevent and reverse the severity of hypertrophic cardiomyopathy. Circ Res. 2006; 98: 540–548.LinkGoogle Scholar8 Stauffer BL, Konhilas JP, Luczak ED, Leinwand LA. Soy diet worsens heart disease in mice. J Clin Invest. 2006; 116: 209–216.CrossrefMedlineGoogle Scholar9 Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation. 2003; 107: 2227–2232.LinkGoogle Scholar10 Jeschke B, Uhl K, Weist B, Schroder D, Meitinger T, Dohlemann C, Vosberg HP. A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated beta-myosin heavy chain genes. Hum Genet. 1998; 102: 299–304.CrossrefMedlineGoogle Scholar11 Hoedemaekers YM, Caliskan K, Majoor-Krakauer D, van de Laar I, Michels M, Witsenburg M, ten Cate FJ, Simoons ML, Dooijes D. Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies. Eur Heart J. 2007; 28: 2732–2737.CrossrefMedlineGoogle Scholar12 Hermida-Prieto M, Monserrat L, Castro-Beiras A, Laredo R, Soler R, Peteiro J, Rodriguez E, Bouzas B, Alvarez N, Muniz J, Crespo-Leiro M. Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. Am J Cardiol. 2004; 94: 50–54.CrossrefMedlineGoogle Scholar13 Sedmera D, Pexieder T, Rychterova V, Hu N, Clark EB. Remodeling of chick embryonic ventricular myoarchitecture under experimentally changed loading conditions. Anat Rec. 1999; 254: 238–252.CrossrefMedlineGoogle Scholar14 Budde BS, Binner P, Waldmuller S, Hohne W, Blankenfeldt W, Hassfeld S, Bromsen J, Dermintzoglou A, Wieczorek M, May E, Kirst E, Selignow C, Rackebrandt K, Muller M, Goody RS, Vosberg HP, Nurnberg P, Scheffold T. Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene. PLoS ONE. 2007; 2: e1362.CrossrefMedlineGoogle Scholar Previous Back to top Next FiguresReferencesRelatedDetailsCited By Wenger T, Chow P, Randle S, Rosen A, Birgfeld C, Wrede J, Javid P, King D, Manh V, Hing A and Albers E (2016) Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A -associated Cornelia de Lange syndrome , American Journal of Medical Genetics Part A, 10.1002/ajmg.a.38030, 173:2, (414-420), Online publication date: 1-Feb-2017. Captur G, Ho C, Schlossarek S, Kerwin J, Mirabel M, Wilson R, Rosmini S, Obianyo C, Reant P, Bassett P, Cook A, Lindsay S, McKenna W, Mills K, Elliott P, Mohun T, Carrier L and Moon J (2016) The embryological basis of subclinical hypertrophic cardiomyopathy, Scientific Reports, 10.1038/srep27714, 6:1, Online publication date: 1-Sep-2016. Caselli S, Attenhofer Jost C, Jenni R and Pelliccia A (2015) Left Ventricular Noncompaction Diagnosis and Management Relevant to Pre-participation Screening of Athletes, The American Journal of Cardiology, 10.1016/j.amjcard.2015.05.055, 116:5, (801-808), Online publication date: 1-Sep-2015. Gerecke B and Engberding R (2012) Die isolierte Noncompaction-Kardiomyopathie unter besonderer Berücksichtigung ihrer rhythmologischen KomplikationenIsolated noncompaction cardiomyopathy with special emphasis on arrhythmia complications, Herzschrittmachertherapie + Elektrophysiologie, 10.1007/s00399-012-0226-6, 23:3, (201-210), Online publication date: 1-Sep-2012. Caleshu C, Sakhuja R, Nussbaum R, Schiller N, Ursell P, Eng C, De Marco T, McGlothlin D, Burchard E and Rame J (2011) Furthering the link between the sarcomere and primary cardiomyopathies: Restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy, American Journal of Medical Genetics Part A, 10.1002/ajmg.a.34097, 155:9, (2229-2235), Online publication date: 1-Sep-2011. Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic B, Ulmer H, Kern M, Katus H and Frey N (2010) Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation, Cardiovascular Research, 10.1093/cvr/cvq009, 86:3, (452-460), Online publication date: 1-Jun-2010., Online publication date: 1-Jun-2010. Gelberg H (2009) Purkinje Fiber Dysplasia (Histiocytoid Cardiomyopathy) with Ventricular Noncompaction in a Savannah Kitten, Veterinary Pathology, 10.1354/vp.08-VP-0291-G-CR, 46:4, (693-697), Online publication date: 1-Jul-2009. Borrás X, Gallego P and Monserrat L (2009) Novedades en cardiología clínica: patología de la aorta, miocardiopatía hipertrófica y profilaxis de la endocarditis infecciosa, Revista Española de Cardiología Suplementos, 10.1016/S1131-3587(09)71770-4, 9:1, (28-38), Online publication date: 1-Jan-2009. Zheng M, Cheng H, Li X, Zhang J, Cui L, Ouyang K, Han L, Zhao T, Gu Y, Dalton N, Bang M, Peterson K and Chen J (2008) Cardiac-specific ablation of Cypher leads to a severe form of dilated cardiomyopathy with premature death, Human Molecular Genetics, 10.1093/hmg/ddn400, 18:4, (701-713), Online publication date: 15-Feb-2009. Borrás X, Gallego P and Monserrat L (2009) Novedades en cardiología clínica: patología de la aorta, miocardiopatía hipertrófica y profilaxis de la endocarditis infecciosa, Revista Española de Cardiología, 10.1016/S0300-8932(09)70039-9, 62, (28-38), Online publication date: 1-Jan-2009. Engberding R, Stöllberger C, Ong P, Yelbuz T, Gerecke B and Breithardt G (2010) Isolated Non-Compaction Cardiomyopathy, Deutsches Ärzteblatt international, 10.3238/arztebl.2010.0206 June 3, 2008Vol 117, Issue 22 Advertisement Article InformationMetrics https://doi.org/10.1161/CIRCULATIONAHA.108.781518PMID: 18519860 Originally publishedJune 3, 2008 KeywordsgeneticssarcomereEditorialscardiomyopathygenesPDF download Advertisement SubjectsCongenital Heart DiseaseGenetics