Research article | Open | Open Peer Review | Published:
Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy
BMC Medical Geneticsvolume 11, Article number: 67 (2010)
MyBPC3 mutations are amongst the most frequent causes of hypertrophic cardiomyopathy, however, its prevalence varies between populations. They have been associated with mild and late onset disease expression. Our objectives were to establish the prevalence of MyBPC3 mutations and determine their associated clinical characteristics in our patients.
Screening by Single Strand Conformation Polymorphisms (SSCP) and sequencing of the fragments with abnormal motility of the MyBPC3 gene in 130 unrelated consecutive HCM index cases. Genotype-Phenotype correlation studies were done in positive families.
16 mutations were found in 20 index cases (15%): 5 novel [D75N, V471E, Q327fs, IVS6+5G>A (homozygous), and IVS11-9G>A] and 11 previously described [A216T, R495W, R502Q (2 families), E542Q (3 families), T957S, R1022P (2 families), E1179K, K504del, K600fs, P955fs and IVS29+5G>A]. Maximum wall thickness and age at time of diagnosis were similar to patients with MYH7 mutations [25(7) vs. 27(8), p = 0.16], [46(16) vs. 44(19), p = 0.9].
Mutations in MyBPC3 are present in 15% of our hypertrophic cardiomyopathy families. Severe hypertrophy and early expression are compatible with the presence of MyBPC3 mutations. The genetic diagnosis not only allows avoiding clinical follow up of non carriers but it opens new possibilities that includes: to take preventive clinical decisions in mutation carriers than have not developed the disease yet, the establishment of genotype-phenotype relationship, and to establish a genetic diagnosis routine in patients with familial HCM.
Hypertrophic Cardiomyopathy (HCM) is an autosomal dominant disorder, characterized by unexplained left ventricular hypertrophy, myocyte hypertrophy and disarray, and interstitial fibrosis [1, 2]. It has a frequency of 0.2% in the adult population and is a major cause of sudden cardiac death (SD) in young people (< 35 years old). Ever since the first mutation in the beta myosin heavy chain (MYH7) gene was described as a cause of hypertrophic cardiomyopathy (HCM) in 1990 , mutations have been identified in 11 genes that codify cardiac sarcomeric proteins [4–7]. Genes that more frequently show mutations are MYH7 and the cardiac myosin binding protein C (MyBPC3) on chromosomes 14 and 11, respectively. Mutations in MyBPC3 are responsible for 15-20% of cases of familial HCM. Besides, available clinical and familial data are very scarce, making it very difficult to confirm the pathogenicity of the described mutations and to establish reliable correlations between genotype and phenotype.
Three isoforms of myosin binding protein-C are known to exist in adult muscle. The three of them have, 10 globular domains termed C1-C10, 7 of which are immunoglobulin I-like (IgI-like) domains, with the remaining three being fibronectin 3 (Fn3) domains. A conserved linker, termed the S2-binding motif, exists between domains C1 and C2. There is also a proline/alanine-rich extension N-terminal of C1. The cardiac isoform has an additional IgI-like domain at the N-terminus (termed C0), an amino acid sequence LAGGGRRIS within the S2-binding motif, and a 28-amino acid insertion within the C5 domain [8, 9]. These domains allow their interaction with other sarcomeric proteins.
The objectives of this study were first, determining the frequency and type of mutations in the MyBPC3 gene within a range of patients with HMC previously studied for the MYH7  gene; second, describing the clinical features of the carriers; and third, analyzing the correlation between genotype and phenotype in the identified mutations.
One hundred and thirty unrelated consecutive index cases from Complejo Hospitalario Universitario A Coruña, Spain, diagnosed with HCM according to the criteria of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases . All the patients had been previously studied for mutations in MYH7 . We did a prospective follow-up which included the search for the patient's personal and family history, symptoms, physical exploration, electrocardiogram, echocardiogram, ergometry, Holter, treatments and events. The family members were invited to a check-up that included a clinical study, electrocardiogram, echocardiogram and genetic study. The clinical characteristics of this cohort had been previously described . All patients and family members signed an informed consent agreement and the study was approved by the "Comité ético de investigación de Galicia". The study protocol conforms to the ethical guidelines of the 2008 Declaration of Helsinki.
(ii) Genetic Study
Genomic DNA was extracted from blood anticoagulated with EDTA with the NUCLEON HT Genomic DNA Extraction Kit (Amersham Biosciences, UK). The primers were designed using reference sequence GenBank:U91629.1. The whole codifying sequence and the flanking intronic regions of the MyBPC3 gene were amplified. Genetic screening was carried out through chain reaction single-strand conformation polymorphism analysis (SSCP) of each fragment using commercial polyacrylamide gels 15/24 (T = 15%, C = 2%-GeneGel-Amersham Biosciences, UK). Each fragment was run to pH 8.3 and pH 9.0. The temperature was optimized for each pH and each fragment. Fragments with abnormal motility were sequenced using automatic sequencer CEQ 8000 Genetic Analysis System (Beckman Coulter, USA). To test the sensitivity of SSCP, the direct sequence analysis of the exon 12 was done for all samples and no false negative results were detected.
A variant was considered a mutation in accordance with three criteria: cosegregation with affected members in the family, absence of the mutation in 200 healthy adult controls, and the conservation of the mutated residue among species.
Moreover, the index cases were studied using Sequenom MassArray™ system where 537 genetic variants of HCM disease genes (TNNT2, TNNI3, TPM1, MYL2, MYL3, ACTC, TTN, MYH6, MYLK2, MYO6, TCAP) were detected by means of MALDI-TOF mass spectrometry after I-PLEX Gold assay (Sequenom Inc.).
(iii) In silicotools
Splice Site Score Predictions
Programs Splicesitefinder (SSF), Alternative Splice Site Predictor (ASSP), NetGene2 v2.4, and Human Splicing Finder splice site analysis (HSF) were used to check if the exon changes affected splice-enhancing sequences, and if the intron changes happened in donor or acceptor splicing sites.
Predicting Damaging Amino Acid Substitution
The substitution is predicted to affect protein function with online programs like Polymorphism Phenotyping (Polyphen), PMUT, and Sorting Intolerant From Tolerant (SIFT).
(iv) Genotype-Phenotype Correlation
A descriptive study of the phenotypical features of the mutation carriers was undertaken. These characteristics were compared with those of relatives without the mutation in order to study cosegregation and penetrance; taking into account both sex and age. Furthermore, features of the carriers were compared with those in cases with identical mutations previously described in medical literature.
Sixteen mutations in MyBPC3 were identified in 20 of the 130 index cases (15%). Thirteen mutations located in exonic regions were concentrated in 8 motives (Figure 1). Seven of them in, or near, motives implicated in myosin and/or titin binding (C0, C1, S2 binding, C7, C8 and linker C9-C10) and the rest of them in motives in which it is unknown if they establish interactions with other proteins. Three mutations (IVS6+5G>A, IVS11-9G>A and IVS29+5G>A) were located in flanking intronic regions and according to the bioinformatics can affect aberrant transcriptions.
Five of the identified mutations were novel whereas the other eleven mutations had been previously described [11–18] (Table 1). All mutations appeared in heterozygousis, except for IVS6+5G>A, which showed up in homozygousis as we have previously reported . None of the patients with mutations in MyBPC3 showed mutations in MYH7.
Three of the sixteen identified mutations were found in more than one family (Table 1). R502Q and R1022P showed up in two families, respectively, and E542Q appeared in three of them.
(i) Comparative between the phenotype of individuals with mutation: MyBPC3 vs. MYH7
There were no significant differences in maximum thickness among index cases with mutations in MyBPC3 (25(7) mm) and MYH7 (27(8) mm), p = 0.16); and age at time of diagnosis was similar (46(16) vs. 44(19) p = 0.9) (Table 2).
(ii) Comparative between the phenotype of individuals with and without mutation
There were significant differences in age at time of diagnosis, abnormal blood pressure response, in maximum left ventricular wall thickness and left atrial diameter between patients with mutation (in MYH7 or MyBPC3) and patients without mutation (Table 2).
Index cases, with mutation were diagnosed younger (p = 0.049), had larger abnormal blood pressure response (p = 0.030), larger left ventricular wall thickness (p = 0.001) and larger left atrial diameter (p = 0.038).
Index cases with mutation had larger frequency of familial history and non-sustained ventricular tachycardia than index cases without mutation, although these differences were not significant.
(iii) Familial genetic study
A genetic study was carried out in 46 positive index cases relatives: 24 were carriers and 22 non-carriers. Out of those 24 carriers, 14 showed HCM, 4 with suggestive electrocardiographic alterations but not HCM diagnostic (H73-II:6 = D75N H197-III:4 = R502Q, H76-II:7 = K504del and H160-IV:2 = P955fs,)], and 6 women, ages 25 (H279-III:2 = V471E), 29 (H95-III:6 = E1179K), 32 (H95-III:2 = E1179K), 33(H131-IV:4 = IVS29+5G>A), 49 (H46-III:4 = K504del) and 68 (H73-II:7 = D75N), were healthy carriers. Within those 22 non-carriers, 18 were considered healthy, 1 with sugestive electrocardiographic alterations (H73-II:3 = D75N), 2 probably affected (H49-IV:1 & IV:5 = R1022P) and 1 case presented HCM (H153-II:1 = E542Q).
SD as the most serious adverse event was prevalent in 5 of the 20 positive index cases. No genetic test was available for these cases. SDs occurred in 2 of 3 families with splice mutations (H56 = IV6+5G>A, H131 = IVS29+5G>A,), in 1 of 3 with frameshift mutations (H160 = P955fs) and in 2 of 9 with missense mutations (H42 = A216T, H166 = E542Q).
Eight individuals of five families suffered from SD between the ages of 15 and 51.
Clinical data of the index cases and carriers can be found in Additional file 1. Figure 2 and figure 3 showed the pedigree of frameshift and splice mutations, and new missense mutations, respectively.
This study has allowed us to identify mutation in MyBPC3 in 15% of our index cases, whereas in MYH7 were 8% in the same cohort . As in other previous studies, the MyBPC3 mutations are more frequently a cause of HCM than mutations in MYH7 [18, 20–23].
In our study, no family presented two mutations in MyBPC3 or in MyBPC3+MYH7. However, previously we have described in this cohort a family with two mutations (R787H and I736T) in MYH7 . This provides us a 0.8% of multiple mutation cases, a lower percentage than the described in the literature (≈ 3%) [18, 24, 25]. As looking for additional mutations, we also tested all patients, using a genotyping platform which included 537 known mutations in other HCM disease genes (TNNT2, TNNI3, TPM1, MYL2, MYL3, ACTC, TTN, MYH6, MYLK2, MYO6, TCAP). None of the index cases in this study had additional mutations in these genes. However, it is possible that there might be new mutations in these genes or mutations in other genes.
The percentages described in this study, 15% for MyBPC3 mutations and 0.8% for multiple mutations, were lower than the described in the literature. The high percentage described could be due to polymorphic variants considered as mutations and the inclusion of related probands. In our study, we considered a variation as a mutation if it was not present in 200 unrelated healthy individuals and our index cases were unrelated.
We have not found significant differences between phenotypes of MyBPC3 and MYH7 carriers, as it has been previously described .
(i) Not previously described mutations
The pathogenicity of the new mutations must be established based upon criteria of cosegregation, absence in health controls, conservation in the evolution and planned functional alteration.
Pathogenicity is very likely in mutations to provoke the introduction of premature stop codons [26, 27], including mutations IVS6+5G>A, IVS11-9G>A, and Q327fs (Table 1 and Figure 2). These truncation mutations could affect protein binding to the thick filament and they could alter the sarcomere's structure and function. In fact, these mutations have been associated to the most severe manifestations of HCM and their association with the disease has been confirmed in animal models [28–30]. However, functional studies of these mutations will be essential to elucidate if they act through a dominant-negative mechanism, if the resulting protein continues to be incorporated into the A-band, or through haploinsufficiency, if the enhanced proteolysis of the truncated protein rather alters the stoichiometry of sarcomeric proteins .
Pathogenicity is more difficult to confirm in new mutations of the missense type (D75N and V471E). These mutations did not show up in 200 healthy controls and they affected conserved residue. Moreover, the use of in silico tools to predict the pathogenicity of missense mutations showed that D75N and V471E were "likely" to be pathological (at least two online programs predicted a damaging effect, Table 1). However, the number of identified carriers is scarce and there are several cases of healthy carriers. The presence of healthy carriers is frequent in the mutations in MyBPC3 due to they can have incomplete penetrance and late development in the hypertrophy . To explain these cases we can speculate that, in the case of V471E, one young healthy women carriers could have had a late onset of the disease expression, and in the case of D75N, as the index cases had been diagnosed at the age of 66, the healthy 68 women could develope HCM in the following years. In favour of their relationship with the disease, we have not identified relatives with HCM who do not carry the mutations. Unless, a relative of D75N index case was probably affected but does not have the mutation; this fact could mean that another factor could be contributing to the development of the HCM.
Therefore, in order to establish the pathogenicity of new mutation, more data about affected and non-affected relatives is needed, and this is not always possible, as in the cases of dead subjects and in those who have declined to participate.
(ii) Previously described mutations
The identification of a known mutation is clinically more useful, because previous information allows for a better evaluation of the pathogenicity and the genotype-phenotype correlation. For example, the familial study in mutation K504del does not let us confirm its pathogenicity (out of four carriers, one is healthy and another one is questionable, Additional file 1), but the existence of 2 previously described families [18, 21] supports the association of the mutation with the disease. In the same way, one of the families with E542Q mutation (H153) has a member who is probably affected and who does not have the mutation. The existence of multiple families in our study (H166, H641) and in other nine families described in the literature [14, 18, 22–24, 32–34] allows us to confirm its association with the disease and it forces us to review its diagnosis (the light-moderate hypertrophy in the electrocardiogram must be confirmed).
Whereas, in mutation R1022P, two possible HCM patients do not have the mutation, and in the case previously described in the literature there are no data about the familial study , so it is not possible to verify its pathogenicity.
On the other hand we provide useful information for the clinicians, like in mutation K600fs (Figure 2), our data confirms the pathogenicity of a previously described mutation in just one case without available clinical data or familial study .
(iii) Severe and early forms of HCM and SD in patients with mutations in MyBPC3
It has been suggested that mutations in gene MyBPC3 are associated with a light clinical and morphological expression and with a late development of hypertrophy [11, 35]. However, we identify a relevant number of cases with early severe hypertrophy development, as in the cases of carriers of the following mutations: R502Q, a post-myectomy 42 year old with 20 mm and another 36 mm case at 15; and P955fs, a 28 mm case at 36 and a 16 year old female with 21 mm. Moreover, we also have cases with atrial fibrillation at a young age (K600fs, R1022P, IVS6+5G>A) and several cases of people who underwent surgery when they were young (R502Q and IVS6+5G>A). Nevertheless, when we gather data about our families and those from previous studies [11, 14, 16, 18, 21–24, 32–35] (Table 3), we see that in several mutations (R502Q, E542Q, K600fs, P955fs) average age at time of diagnosis is not advanced and thickness is above average in HCM.
HCM has been recognized as the most common cause of SD in the young, especially in competitive athletes . The families associated with SD presented missense mutations (A216T, E542Q) and mutations that lead to aberrant transcripts (P955fs, IVS6+5G>A, IVS29+5G>A).
The association between SD and missense mutations A216T and E542Q is controversial; probably there are other additional factors that can be interacting. The index case of A216T was a woman with HCM and thrombotic problems (she needed two surgical aortic valve replacements and finally went into heart transplantation). On the other hand, the E542Q mutation was present in 3 of our 130 families, but only in one of them has cases of SD.
In our families the most strong association of SD with the mutations is in the mutations that lead to protein truncation (P955fs, IVS6+5G>A, IVS29+5G>A). In fact, the youngest SD (15 and 26 year old) are in the IVS6+5G>A index cases families, and these individuals are likely to be in homozygousis as in the index case. This fact could support a gene dossage effect for mutations in the MyBPC3 gene that have been previously described where a homozygous mutation is associated with a more severe phenotype than the heterozygous .
We have identified mutations in MyBPC3 in 15% of our families with HCM. Severe hypertrophy and an early expression of the disease are compatible with the presence of mutations in MyBPC3.
Genetic studies can play a key role in the comprehensive evaluation of familiar hypertrophic cardiomyopathy and in the development of individualized medicine. This kind of analysis not only allows avoiding clinical follow up of non carriers but it opens new possibilities including: taking preventive clinical decisions in mutation carriers than have not developed the disease yet, the establishment of genotype-phenotype relationship, and establishing a genetic diagnosis routine in patients with familial HCM.
To obtain these purposes, it is important to perform the genetic analysis of index cases and in a high number of their relatives. It is necessary to obtain detailed data about the phenotype of a larger number of carriers, and to complete the genetic study in the severe cases through analysis of other genes in order to establish in which degree the severity of the phenotypes is a feature of the identified mutations or if it depends upon additional factors.
Maron BJ, McKenna WJ, Danielson GK, Kappenberger LJ, Kuhn HJ, Seidman CE, Shah PM, Spencer WH, Spirito P, Ten Cate FJ, Wigle ED, Task Force on Clinical Expert Consensus Documents American College of Cardiology; Committee for Practice Guidelines European Society of Cardiology American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy: A report of American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines. Eur Heart J. 2003, 24: 1965-1991. 10.1016/S0195-668X(03)00479-2.
Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuwelt S, Rapezzi C, Seferovic P, Tavazzi L, 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: 270-276. 10.1093/eurheartj/ehm342.
Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG: A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene missense mutation. Cell. 1990, 62: 999-1006. 10.1016/0092-8674(90)90274-I.
Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE: Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat Genet. 1995, 11: 434-437. 10.1038/ng1295-434.
Seidman JG, Seidman C: The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell. 2001, 104: 557-567. 10.1016/S0092-8674(01)00242-2.
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. 10.1161/CIRCULATIONAHA.105.547448.
Lind JM, Chiu C, Semsarian C: Genetic basis of hypertrophic cardiomyopathy. Expert Rev Cardiovasc Ther. 2006, 4: 927-934. 10.1586/14779072.4.6.927.
Winegrad S: Cardiac myosin binding protein C. Circ Res. 1999, 84: 1117-1126.
Flashman E, Redwood C, Moolman-Smook J, Watkins H: Cardiac Myosin Binding Protein C: Its role in Physiology and Disease. Circ Res. 2004, 94: 1279-1289. 10.1161/01.RES.0000127175.21818.C2.
Laredo R, Monserrat L, Hermida-Prieto M, Fernández X, Rodríguez I, Cazón L, Alvariño I, Dumont C, Piñón P, Peteiro J, Bouzas B, Castro-Beiras A: Beta-Myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy. Rev Esp Cardiol. 2006, 59: 1008-1018. 10.1157/13093977.
Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna WJ, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE: Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med. 1998, 338: 1248-1257. 10.1056/NEJM199804303381802.
Fokstuen S, Lyle R, Munoz A, Gehrig C, Lerch R, Perrot A, Osterziel KJ, Geier C, Beghetti M, Mach F, Sztajzel J, Sigwart U, Antonarakis SE, Blouin JL: A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy. Hum Mutat. 2008, 29: 879-885. 10.1002/humu.20749.
Garcia-Castro M, Coto E, Reguero J, Berrazueta JR, Alvarez V, Alonso B, Sainz R, Martin M, Moris C: Espectro mutacional de los genes sarcomericos MYH7, MYBPC3, TNNT2, TNNI3 y TPM1 en pacientes con miocardiopatia hipertrofica. Rev Esp Cardiol. 2009, 62: 48-56. 10.1016/S1885-5857(09)71513-0.
Carrier L, Bonne G, Bahrend E, Yu B, Richard P, Niel F, Hainque B, Cruard C, Gary F, Labiet S, Bouhour JB, Dubourg O, Desnos M, Hagege A, Trent RJ, Komajga M, Fiszman M, Schwartz K: Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ Res. 1997, 80: 427-434.
Ehlermann P, Weichenhan D, Zehelein J, Steen H, Pribe R, Zeller R, Lehrke S, Zugck C, Ivandic BT, Katus HA: Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene. BMC Med Genet. 2008, 9: 95-10.1186/1471-2350-9-95.
Brito D, Madeira H: Malignant mutations in hypertrophic cardiomyopathy: fact or fancy?. Rev Port Cardiol. 2005, 24: 1137-1146.
Brion M, Allegue C, Gil R, Torres M, Santori M, Poster S, Madea B, Carracedo A: Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS). Forensic Sci Int: Genet Suppl. 2009, 2: 495-496. 10.1016/j.fsigss.2009.09.040.
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: EUROGENE Heart Failure Project Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation. 2003, 107: 2227-2232. 10.1161/01.CIR.0000066323.15244.54.
Ortiz M, Rodriguez-Garcia MI, Hermida-Prieto M, Fernández X, Veira E, Barriales-Villa R, Castro-Beiras A, Monserrat L: Mutación en homocigosis en el gen MYBPC3 asociada a fenotipos severos y alto riesgo de muerte súbita en una familia con miocardiopatía hipertrófica. Rev Esp Cardiol. 2009, 62: 572-575. 10.1016/S1885-5857(09)71841-9.
Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Pedersen AK, Kjeldsen K, Christiansen M: Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency. Eur J Hum Genet. 2004, 12: 673-677. 10.1038/sj.ejhg.5201190.
Cardim N, Perrot A, Santos S, Morgado P, Padua M, Ferreira S, Reis RP, Monteiro C, Ferreira T, Correia JM, Osterziel KJ: Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C gene. Rev Port Cardiol. 2005, 24: 1463-1476.
Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C: Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling. J Med Genet. 2005, 42: e59-10.1136/jmg.2005.033886.
Olivotto I, Girolami F, Ackerman MJ, Nistri S, Bos JM, Zachara E, Ommen SR, Theis JL, Vaubel RA, Re F, Armentano C, Poggesi C, Torricelli F, Cecchi F: Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy. Mayo Clinic Proceedings. 2008, 83: 630-638. 10.4065/83.6.630.
Van Driest SL, Vasile VC, Ommen SR, Will ML, Tajik AJ, Gersh BJ, Ackerman MJ: Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004, 44: 1903-1910. 10.1016/j.jacc.2004.07.045.
Van Driest SL, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ: Sarcomeric genotyping in hypertrophic cardiomyopathy. Mayo Clin Proc. 2005, 80: 463-469. 10.4065/80.4.463.
Bonne G, Carrier L, Richard P, Hainque B, Schwartz K: Familial Hypertrophic Cardiomyopathy: From Mutations to Functional Defects. Circ Res. 1998, 83: 580-593.
Erdmann J, Raible J, Maki-Abadi J, Hummel M, Hammann J, Wollnik B, Frantz E, Fleck E, Hetzer R, Regitz-Zagrosek V: Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy. J Am Coll Cardiol. 2001, 38: 322-330. 10.1016/S0735-1097(01)01387-0.
Yang Q, Sanbe A, Osinska H, Hewett TE, Klevitsky R, Robbins J: A mouse model of myosin binding protein C human familial hypertrophic cardiomyopathy. J Clin Invest. 1998, 102: 1292-1300. 10.1172/JCI3880.
McConnell BK, Fatkin D, Semsarian C, Jones KA, Georgakopoulos D, Maguire CT, Healey MJ, Mudd JO, Moskowitz IP, Conner DA, Giewat M, Wakimoto H, Berul CI, Schoen FJ, Kass DA, Seidman CE, Seidman JG: Comparison of two murine models of familial hypertrophic cardiomyopathy. Circulation Research. 2001, 88: 383-389.
Harris SP, Bartley CR, Hacker TA, McDonald KS, Douglas PS, Greaser ML, Powers PA, Moss RL: Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice. Circulation Research. 2002, 90: 594-601. 10.1161/01.RES.0000012222.70819.64.
Nanni L, Pieroni M, Chimenti C, Simionati B, Zimbello R, Maseri A, Frustaci A, Lanfranchi G: Hypertrophic cardiomyopathy: two homozygous cases with "typical" hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy. Biochem Biophys Res Commun. 2003, 309: 391-398. 10.1016/j.bbrc.2003.08.014.
Charron P, Dubourg O, Desnos M, Bennaceur M, Carrier L, Camproux AC, Isnard R, Hagege A, Langlard JM, Bonne G, Richard P, Hainque B, Bouhour JB, Schwartz K, Komajda M: Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene. Circulation. 1998, 97: 2230-2236.
Charron P, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagege A, Carrier L, Bonne G, Tesson F, Richard P, Hainque B, Schwartz K, Komajda M: Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children. Eur Heart J. 1998, 19: 1377-1382. 10.1053/euhj.1998.1049.
Flavigny J, Souchet M, Sebillon P, Berrebi-Bertrand I, Uainque B, Maller A, Bril A, Schwartz K, Carrier L: COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes. J Mol Biol. 1999, 94: 443-456. 10.1006/jmbi.1999.3276.
Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE: Shared genetic causes of cardiac hypertrophy in children and adults. N Engl J Med. 2008, 358: 1899-1908. 10.1056/NEJMoa075463.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2350/11/67/prepub
We thank Inés Alvariño for the technical support.
This study has been funded by a FIS PI070926 project from the Instituto de Salud Carlos III.
Martín Ortiz received funding as a research fellow from Fundación Carolina-BBVA.
The authors declare that they have no competing interests.
LM and MHP conceived and designed the study. MIRG carried out the molecular genetic studies, participated in the sequence alignment and drafted the manuscript. LC, LN and EM participated in the sequence alignment. LM, MO, XF, RBV and EV acquired and interpreted the clinical data. ACB handled funding and supervised the study. Finally, MIRG, LM, LN and MHP drafted the manuscript. All authors read and approved the final manuscript.