RESUMO

Background: Hypertrophic phenotype cardiomyopathy is the most common heart disease in cats. Although the echocardiogram is the gold standard test for diagnosing fHCM, patients with the disease may have electrocardiographic changes. Despite being reported in most 12-lead electrocardiograms, the P wave axis generally receives little attention when compared to other wave parameters. We performed a Doppler echocardiographic and electrocardiographic study in cats, in order to verify the presence of correlation between the electrical axis average P wave and the presence of fCMH, aiming to investigate the possibility of its aid in the early diagnosis of cardiac disorders. Materials, Methods & Results: One hundred cats of different breeds, ages, males and females were evaluated. Those animals with a history of previous disease other than hypertrophic cardiomyopathy were excluded from the study. The groups were formed after obtaining the results of the echocardiographic examination. Eight of the 100 cats did not allow echocardiographic evaluation, and the remaining 92 were divided into 2 groups (control group, n = 64 and heart disease group, n = 28) after the examination. Of these 92 animals, 28 cats had the hypertrophic cardiomyopathy phenotype. The electrocardiographic examination was performed after the allocation of animals into groups lasting 5 min with the recording of tracings for later interpretation. To calculate the axis of the P wave, leads D1 and D3 were used, measuring the amplitude of the P wave in these leads and calculating the resulting amplitude. All cats studied had mean electrical axis of the P wave within the normal range for the species (0º to 90º). Based on mean electrical axis P wave values, there was no significant difference between groups. The control group had a median of 63.7° with a maximum value of 80°, a minimum value of 60° and a mean of 65.1°. The fCMH group had a median of 68.7° with a maximum value of 85.3°, a minimum value of 56.3° and a mean of 68.8°. Of the fCMH group, 3 cats had increased P wave duration (50.33 ± 5.77 ms), suggesting left atrial overload, and 13 cats had increased QRS complex duration (66.30 ± 11.23 ms). Also, 18 cats (Control group: 11; fCMH group: 7) showed T wave amplitude greater than 25% of R, suggesting the presence of myocardial hypoxia and/or electrolyte disturbance. One cat had a prolonged PR interval (from the fCMH group). As for the QT interval, 6 cats had an interval < 120 (2 from the control group and 4 from the affected group) and 3 had an interval > 180 (1 from the control group and 2 from the affected group). The ST segment remained isoelectric in all segments. As for the mean electrical axis of the QRS complex, 5 cats (10.42%) had axis deviation to the right (control: 1; fCMH: 4) suggesting right ventricular overload; 7 cats (14.58%) had left axis deviation (control: 5; fCMH: 2), suggestive of left ventricular overload; and 36 cats (75%) had a normal mean electrical axis. Discussion: Based on the results obtained in the present study, it can be concluded that screening studies in asymptomatic felines should be increasingly implemented in the veterinary clinical routine, since the frequency found was high (30.44%) and that patients may remain asymptomatic for years until the development of signs. It should be concluded that there was no correlation between the mean electric axis of P-wave and the presence of subclinical phenotype hypertrophic cardiomyopathy. Therefore, more studies are needed, with felines at different stages of the disease, to evaluate whether this electrocardiographic measurement allows us to assist in its diagnosis, since it is a feasible measure in cats. Furthermore, it is concluded that the electrocardiogram should be used as an aid method in the diagnosis of the disease and not as a screening test.

Assuntos

RESUMO

Dilated cardiomyopathy (DCM) is characterized by systolic myocardial dysfunction which is identified by low myocardial velocities obtained by pulsed tissue Doppler (PTD). However, increased preload is known to increase myocardial velocities which could overestimate myocardial function and turn dysfunction characterization into a challenge in dogs with DCM and congestive heart failure. To test the hypothesis that increased preload could hamper identification of low myocardial velocities in dogs with DCM and congestive heart failure the present study prospectively evaluated 32 English Cocker Spaniel dogs, being 16 with clinical DCM and 16 healthy for control purpose. The PTD analysis of regional velocities were performed in both longitudinal and radial myocardial displacements and systolic (Sm), early (Em) and late diastolic (Am) velocities were obtained in left ventricular free wall (LVFW) and interventricular septum (IVS). Peak radial subendocardial and subepicardial Sm velocities were lower in DCM group compared to control (0.065±0.018 vs. 0.102±0.020m/s and 0.059±0.014 vs. 0.094±0.025m/s respectively; p<0.001). Peak longitudinal Sm velocities were lower in basal and medial portions of LVFW (0.093±0.034 vs. 0.155±0.034m/s and 0.091±0.033 vs. 0.134±0.037m/s respectively; p<0.001) and IVS (0.063±0.021 vs. 0.136±0.039 and 0.066±0.026 vs. 0.104±0.032m/s respectively; p<0.001). Most of diastolic velocities were not significantly different between groups, although advanced myocardial disease and dysfunction are expected in DCM group. Reduction in systolic basal and medial longitudinal myocardial velocities and in radial myocardial velocities was the most significant PTD findings. Increased preload did not represent a problem to evaluate systolic dysfunction by PTD in English Cocker Spaniels with DCM, but influence of preload on assessment of diastolic velocities should be better elucidated.(AU)

A cardiomiopatia dilatada (CMD) é caracterizada por disfunção miocárdica sistólica, a qual pode ser identificada pelas baixas velocidades miocárdicas obtidas por meio de Doppler tecidual pulsátil (DTP). Contudo, sabe-se que a elevada pré-carga aumenta as velocidades miocárdicas, o que poderia superestimar a função miocárdica e tornar desafiadora a caracterização da disfunção nos cães com CMD e insuficiência cardíaca congestiva. Para testar a hipótese de que a elevada pré-carga pode mascarar a identificação de baixas velocidades miocárdicas nos cães com CMD e insuficiência cardíaca congestiva, o presente estudo avaliou prospectivamente 32 cães da raça Cocker Spaniel Inglês, sendo 16 com manifestações clínicas de CMD e 16 hígidos para efeito de grupo controle. A análise DTP das velocidades regionais foi realizada tanto no deslocamento miocárdico longitudinal quanto radial e foram obtidas as velocidades sistólica (Sm), diastólica inicial (Em) e tardia (Am) na parede livre do ventrículo esquerdo (PLVE) e no septo interventricular (SIV). Os valores de Sm radial subendocárdicos e subepicárdicos foram menores no grupo CMD em comparação com o grupo controle (0,065±0,018 vs. 0,102±0,020m/s e 0,059±0,014 vs. 0,094±0,025m/s, respectivamente; p<0,001). Os valores de Sm longitudinais foram menores nas porções basal e intermediária da parede do ventrículo esquerdo (0,093±0,034 vs. 0,155±0,034m/s e 0,091±0,033 vs. 0,134±0,037m/s, respectivamente; p<0,001) e do septo interventricular (0,063±0,021 vs. 0,136±0,039 e 0,066±0,026 vs. 0,104±0,032m/s, respectivamente; p<0.001). A maioria dos índices diastólicos não apresentou diferença significativa entre os grupos, apesar de a doença miocárdica avançada e a disfunção serem esperadas no grupo CMD. A redução nas velocidades sistólicas longitudinais nos segmentos basais e intermediários e nas velocidades radiais representaram os achados mais relevantes no estudo com DTP. Nos cães da raça Cocker Spaniel Inglês com CMD e insuficiência cardíaca congestiva a pré-carga elevada não representou empecilho para a avaliação da disfunção sistólica por meio de DTP, porém a influência da pré-carga na avaliação das velocidades diastólicas deve ser mais bem investigada.(AU)

Assuntos

RESUMO

Dilated cardiomyopathy (DCM) is characterized by systolic myocardial dysfunction which is identified by low myocardial velocities obtained by pulsed tissue Doppler (PTD). However, increased preload is known to increase myocardial velocities which could overestimate myocardial function and turn dysfunction characterization into a challenge in dogs with DCM and congestive heart failure. To test the hypothesis that increased preload could hamper identification of low myocardial velocities in dogs with DCM and congestive heart failure the present study prospectively evaluated 32 English Cocker Spaniel dogs, being 16 with clinical DCM and 16 healthy for control purpose. The PTD analysis of regional velocities were performed in both longitudinal and radial myocardial displacements and systolic (Sm), early (Em) and late diastolic (Am) velocities were obtained in left ventricular free wall (LVFW) and interventricular septum (IVS). Peak radial subendocardial and subepicardial Sm velocities were lower in DCM group compared to control (0.065±0.018 vs. 0.102±0.020m/s and 0.059±0.014 vs. 0.094±0.025m/s respectively; p 0.001). Peak longitudinal Sm velocities were lower in basal and medial portions of LVFW (0.093±0.034 vs. 0.155±0.034m/s and 0.091±0.033 vs. 0.134±0.037m/s respectively; p 0.001) and IVS (0.063±0.021 vs. 0.136±0.039 and 0.066±0.026 vs. 0.104±0.032m/s respectively; p 0.001). Most of diastolic velocities were not significantly different between groups, although advanced myocardial disease and dysfunction are expected in DCM group. Reduction in systolic basal and medial longitudinal myocardial velocities and in radial myocardial velocities was the most significant PTD findings. Increased preload did not represent a problem to evaluate systolic dysfunction by PTD in English Cocker Spaniels with DCM, but influence of preload on assessment of diastolic velocities should be better elucidated.(AU)

A cardiomiopatia dilatada (CMD) é caracterizada por disfunção miocárdica sistólica, a qual pode ser identificada pelas baixas velocidades miocárdicas obtidas por meio de Doppler tecidual pulsátil (DTP). Contudo, sabe-se que a elevada pré-carga aumenta as velocidades miocárdicas, o que poderia superestimar a função miocárdica e tornar desafiadora a caracterização da disfunção nos cães com CMD e insuficiência cardíaca congestiva. Para testar a hipótese de que a elevada pré-carga pode mascarar a identificação de baixas velocidades miocárdicas nos cães com CMD e insuficiência cardíaca congestiva, o presente estudo avaliou prospectivamente 32 cães da raça Cocker Spaniel Inglês, sendo 16 com manifestações clínicas de CMD e 16 hígidos para efeito de grupo controle. A análise DTP das velocidades regionais foi realizada tanto no deslocamento miocárdico longitudinal quanto radial e foram obtidas as velocidades sistólica (Sm), diastólica inicial (Em) e tardia (Am) na parede livre do ventrículo esquerdo (PLVE) e no septo interventricular (SIV). Os valores de Sm radial subendocárdicos e subepicárdicos foram menores no grupo CMD em comparação com o grupo controle (0,065±0,018 vs. 0,102±0,020m/s e 0,059±0,014 vs. 0,094±0,025m/s, respectivamente; p 0,001). Os valores de Sm longitudinais foram menores nas porções basal e intermediária da parede do ventrículo esquerdo (0,093±0,034 vs. 0,155±0,034m/s e 0,091±0,033 vs. 0,134±0,037m/s, respectivamente; p 0,001) e do septo interventricular (0,063±0,021 vs. 0,136±0,039 e 0,066±0,026 vs. 0,104±0,032m/s, respectivamente; p 0.001). A maioria dos índices diastólicos não apresentou diferença significativa entre os grupos, apesar de a doença miocárdica avançada e a disfunção serem esperadas no grupo CMD. A redução nas velocidades sistólicas longitudinais nos segmentos basais e intermediários e nas velocidades radiais representaram os achados mais relevantes no estudo com DTP. [...](AU)

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RESUMO

Hypertrophic cardiomyopathy (HCM) is the most common feline heart disease and is characterized by increased cardiac mass with a hypertrophied nondilated left ventricle. Myocardial dysfunction occurs in cats with HCM but less is known about dysfunctions in initial stages of HCM. A mutation in MYBPC-A31P gene has been identified in a colony of Maine Coon cats with HCM. However, the close correlation between genotype and phenotype still be inconclusive. Myocardial analysis by tissue Doppler imaging (TDI) is a noninvasive echocardiographic method to assess systolic and diastolic function that is more sensitive than conventional echocardiography. To evaluate diastolic and systolic function in cats with mutation, with or without ventricular hypertrophy, Maine Coon cats (n=57) were screened for mutation and examined with both echocardiography and TDI (pulsed tissue Doppler and color tissue Doppler methods). Then, were phenotypically classified in: normal (n=45), suspects (n=7) and HCM group (n=5); and genotypically classified in: negative (n=28), heterozygous (n=26) and homozygous group (n=3). Myocardial velocities (by pulsed and color tissue Doppler imaging) measured in the basal and mildventricular segment of the interventricular septal wall (IVS), left ventricular free wall (LVW), left ventricular anterior wall (LVAW), left ventricular posterior wall (LVPW) and radial segment of LVW, was compared among different groups. A decreased longitudinal Em velocities (pulsed tissue Doppler) at the mildventricular segment of LVW was observed in HCM cats compared with suspects and normal cats. A decreased longitudinal Em/Am (color tissue Doppler) at the basal segment of IVS was observed in HCM cats compared with suspects and normal cats. A significant increased longitudinal E/Em (color tissue Doppler) at the basal segment of IVS was observed in HCM cats compared with suspects and normal cats. And a significant decreased longitudinal Sm (color tissue Doppler) at the basal segment of the LVW was observed in heterozygous cats compared with negative cats, both without hypertrophy. There was a positive correlation between summated early and late diastolic velocities (Em/Am) and heart rate; and a positive correlation between Sm and Em velocities and heart rate, both in pulsed and in color TDI. TDI analyses are a new, valuable and reproducible method in cats that alone is not able to identify cats with mutation before myocardial hypertrophy. Despite high expectations regarding the use of TDI for early identification of individuals with HCM, there is still need for larger studies with greater numbers of individuals.

A cardiomiopatia hipertrófica (CMH) é a principal cardiopatia dos felinos e é caracterizada por hipertrofia miocárdica concêntrica, sem dilatação ventricular. Disfunções miocárdicas ocorrem em gatos com CMH, mas pouco se conhece a respeito destas alterações nos estágios iniciais da afecção. Em gatos da raça Maine Coon, a mutação no gene MyBPC-A31P está relacionada com a CMH de origem familial, porém, a correlação exata entre o genótipo e o fenótipo ainda é inconclusiva. A ecocardiografia tecidual é uma modalidade não invasiva que permite avaliação da função miocárdica e é mais sensível que a ecocardiografia convencional. Para avaliar as funções sistólica e diastólica, antes ou após a ocorrência de hipertrofia ventricular, gatos da raça Maine Coon (n=57), geneticamente testados para a mutação, foram avaliados por meio de ecocardiografias convencional e tecidual (nas modalidades Doppler tecidual pulsado e Doppler tecidual colorido). Posteriormente, foram fenotipicamente classificados em: normais (n=45), suspeitos (n=7) e acometidos pela CMH (n=5); e genotipicamente classificados em: negativos (n=28), heterozigotos (n=26) e homozigotos para a mutação (n=3). Valores de velocidades miocárdicas (Doppler tecidual pulsado e colorido) medidos na região basal e média do septo interventricular (SIV), da parede livre do ventrículo esquerdo (PVE), da parede anterior do ventrículo esquerdo (PAVE), da parede posterior do ventrículo esquerdo (PPVE) e do segmento radial da PVE, foram comparados nos diferentes grupos. Observou-se que as velocidades longitudinais Em (Doppler tecidual pulsado) na região média da PVE foram menores nos gatos com CMH quando comparados com suspeitos e normais. Os valores de Em/Am (Doppler tecidual colorido), na região basal do SIV, foram inferiores nos gatos com CMH quando comparados com suspeitos e normais. A relação E/Em (Doppler tecidual colorido), na região basal do SIV, foi maior nos gatos com CMH em relação aos suspeitos e normais, enquanto que os valores de Sm (Doppler tecidual colorido), em região basal da PVE, foram menores nos gatos heterozigotos quando comparados com os negativos, ambos sem hipertrofia ventricular. Observou-se correlação positiva entre a ocorrência de fusão das ondas Em e Am e a frequência cardíaca, assim como correlação positiva entre valores de Sm e Em e a frequência cardíaca (Doppler tecidual pulsado e colorido). A ecocardiografia tecidual é uma nova modalidade ecocardiográfica reprodutível em gatos que, isoladamente, não permite diferenciar gatos portadores da mutação antes do desenvolvimento de hipertrofia ventricular. Apresenta utilidade como auxílio no diagnóstico em fases iniciais, mas, apesar da expectativa para a identificação precoce de indivíduos portadores da CMH, ainda há necessidade de estudos mais extensos e com maior número de indivíduos.

Assuntos

RESUMO

Hypertrophic cardiomyopathy (HCM) is the most common feline heart disease and is characterized by increased cardiac mass with a hypertrophied nondilated left ventricle. Myocardial dysfunction occurs in cats with HCM but less is known about dysfunctions in initial stages of HCM. A mutation in MYBPC-A31P gene has been identified in a colony of Maine Coon cats with HCM. However, the close correlation between genotype and phenotype still be inconclusive. Myocardial analysis by tissue Doppler imaging (TDI) is a noninvasive echocardiographic method to assess systolic and diastolic function that is more sensitive than conventional echocardiography. To evaluate diastolic and systolic function in cats with mutation, with or without ventricular hypertrophy, Maine Coon cats (n=57) were screened for mutation and examined with both echocardiography and TDI (pulsed tissue Doppler and color tissue Doppler methods). Then, were phenotypically classified in: normal (n=45), suspects (n=7) and HCM group (n=5); and genotypically classified in: negative (n=28), heterozygous (n=26) and homozygous group (n=3). Myocardial velocities (by pulsed and color tissue Doppler imaging) measured in the basal and mildventricular segment of the interventricular septal wall (IVS), left ventricular free wall (LVW), left ventricular anterior wall (LVAW), left ventricular posterior wall (LVPW) and radial segment of LVW, was compared among different groups. A decreased longitudinal Em velocities (pulsed tissue Doppler) at the mildventricular segment of LVW was observed in HCM cats compared with suspects and normal cats. A decreased longitudinal Em/Am (color tissue Doppler) at the basal segment of IVS was observed in HCM cats compared with suspects and normal cats. A significant increased longitudinal E/Em (color tissue Doppler) at the basal segment of IVS was observed in HCM cats compared with suspects and normal cats. And a significant decreased longitudinal Sm (color tissue Doppler) at the basal segment of the LVW was observed in heterozygous cats compared with negative cats, both without hypertrophy. There was a positive correlation between summated early and late diastolic velocities (Em/Am) and heart rate; and a positive correlation between Sm and Em velocities and heart rate, both in pulsed and in color TDI. TDI analyses are a new, valuable and reproducible method in cats that alone is not able to identify cats with mutation before myocardial hypertrophy. Despite high expectations regarding the use of TDI for early identification of individuals with HCM, there is still need for larger studies with greater numbers of individuals.(AU)

A cardiomiopatia hipertrófica (CMH) é a principal cardiopatia dos felinos e é caracterizada por hipertrofia miocárdica concêntrica, sem dilatação ventricular. Disfunções miocárdicas ocorrem em gatos com CMH, mas pouco se conhece a respeito destas alterações nos estágios iniciais da afecção. Em gatos da raça Maine Coon, a mutação no gene MyBPC-A31P está relacionada com a CMH de origem familial, porém, a correlação exata entre o genótipo e o fenótipo ainda é inconclusiva. A ecocardiografia tecidual é uma modalidade não invasiva que permite avaliação da função miocárdica e é mais sensível que a ecocardiografia convencional. Para avaliar as funções sistólica e diastólica, antes ou após a ocorrência de hipertrofia ventricular, gatos da raça Maine Coon (n=57), geneticamente testados para a mutação, foram avaliados por meio de ecocardiografias convencional e tecidual (nas modalidades Doppler tecidual pulsado e Doppler tecidual colorido). Posteriormente, foram fenotipicamente classificados em: normais (n=45), suspeitos (n=7) e acometidos pela CMH (n=5); e genotipicamente classificados em: negativos (n=28), heterozigotos (n=26) e homozigotos para a mutação (n=3). Valores de velocidades miocárdicas (Doppler tecidual pulsado e colorido) medidos na região basal e média do septo interventricular (SIV), da parede livre do ventrículo esquerdo (PVE), da parede anterior do ventrículo esquerdo (PAVE), da parede posterior do ventrículo esquerdo (PPVE) e do segmento radial da PVE, foram comparados nos diferentes grupos. Observou-se que as velocidades longitudinais Em (Doppler tecidual pulsado) na região média da PVE foram menores nos gatos com CMH quando comparados com suspeitos e normais. Os valores de Em/Am (Doppler tecidual colorido), na região basal do SIV, foram inferiores nos gatos com CMH quando comparados com suspeitos e normais. A relação E/Em (Doppler tecidual colorido), na região basal do SIV, foi maior nos gatos com CMH em relação aos suspeitos e normais, enquanto que os valores de Sm (Doppler tecidual colorido), em região basal da PVE, foram menores nos gatos heterozigotos quando comparados com os negativos, ambos sem hipertrofia ventricular. Observou-se correlação positiva entre a ocorrência de fusão das ondas Em e Am e a frequência cardíaca, assim como correlação positiva entre valores de Sm e Em e a frequência cardíaca (Doppler tecidual pulsado e colorido). A ecocardiografia tecidual é uma nova modalidade ecocardiográfica reprodutível em gatos que, isoladamente, não permite diferenciar gatos portadores da mutação antes do desenvolvimento de hipertrofia ventricular. Apresenta utilidade como auxílio no diagnóstico em fases iniciais, mas, apesar da expectativa para a identificação precoce de indivíduos portadores da CMH, ainda há necessidade de estudos mais extensos e com maior número de indivíduos.(AU)

Assuntos