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1.
Int J Cardiovasc Imaging ; 37(2): 379-388, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-32959094

RESUMEN

The success rate of percutaneous coronary artery intervention (PCI) of chronic total occlusion (CTO) lesions have increased in the recent years. However, improvement of function is only possible when significant myocardial viability is present. One of the most important factors of maintaining myocardial viability is the opening and development of collaterals. Our hypothesis was that with a higher degree of collaterals more viable myocardium is present. In 38 patients we compared the degree of collaterals, evaluated with a conventional coronary angiogram (CCA) and graded by the Rentrop classification to transmural extent of the scar obtained in a viability study with magnetic resonance (MRI). We found a statistically significant association of the degree of collaterals determined with Rentrop method and transmural extent of the scar as measured by CMR (p = 0.001; Tau = -0.144). Additionally, associations showed an increase in the ratio between viable vs. non-viable myocardium with the degree of collaterals. Our study suggests that it may be beneficial to routinely grade the collaterals at angiography in patients with CTO as an assessment of myocardial viability.


Asunto(s)
Circulación Colateral , Angiografía Coronaria , Circulación Coronaria , Oclusión Coronaria/diagnóstico por imagen , Vasos Coronarios/diagnóstico por imagen , Imagen por Resonancia Cinemagnética , Miocardio/patología , Anciano , Enfermedad Crónica , Oclusión Coronaria/patología , Oclusión Coronaria/fisiopatología , Vasos Coronarios/fisiopatología , Femenino , Fibrosis , Humanos , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Reproducibilidad de los Resultados , Estudios Retrospectivos , Supervivencia Tisular
2.
Circ Cardiovasc Genet ; 5(5): 490-502, 2012 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-22923418

RESUMEN

BACKGROUND: X-linked myopathy with postural muscle atrophy is a novel X-linked myopathy caused by mutations in the four-and-a-half LIM domain 1 gene (FHL1). Cardiac involvement was suspected in initial publications. We now systematically analyzed the association of the FHL1 genotype with the cardiac phenotype to establish a potential cardiac involvement in the disease. METHODS AND RESULTS: Seventeen male patients and 23 female mutation carriers were compared with healthy controls. Every patient underwent a comprehensive clinical and cardiovascular workup. ECG abnormalities occurred frequently in affected males and were less frequent in heterozygous females. Both male and female mutation carriers had increased myocardial mass (affected males=115.1±25.3 g/m(2); heterozygous females=95.1±19.6 g/m(2); controls=89.0±15.6 g/m(2) and 72.6±12.6 g/m(2); respectively) with increased wall thickness (typically midventricular and apical segments) mainly in affected males. Longitudinal systolic function was reduced in affected males (radial systolic strain: affected males=24.6±11.8%; male controls=43.2±14.8%; P=0.002). Diastolic dysfunction occurred in both affected males and heterozygous females. Cardiac MRI revealed a morphological hallmark of X-linked myopathy with postural muscle atrophy; a characteristic spongious structure and replacement fibrosis indicated by late enhancement could be detected in most affected males. X-linked myopathy with postural muscle atrophy was associated with reduced exercise capacity in affected males but not in heterozygous female mutation carriers. CONCLUSIONS: X-linked myopathy with postural muscle atrophy patients consistently showed electrical, functional, and characteristic morphological cardiac abnormalities that translate into reduced exercise capacity. Reduced systolic and diastolic function is associated with a novel type of spongious hypertrophic cardiomyopathy. An unexpected finding was that some cardiac abnormalities were also present in heterozygous female mutation carriers.


Asunto(s)
Cardiomiopatía Hipertrófica/genética , Péptidos y Proteínas de Señalización Intracelular/genética , Proteínas con Dominio LIM/genética , Proteínas Musculares/genética , Adulto , Anciano , Secuencia de Aminoácidos , Presión Sanguínea/fisiología , Cardiomiopatía Hipertrófica/fisiopatología , Electrocardiografía , Femenino , Genes Ligados a X , Genotipo , Heterocigoto , Humanos , Péptidos y Proteínas de Señalización Intracelular/química , Proteínas con Dominio LIM/química , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular , Proteínas Musculares/química , Distrofia Muscular de Emery-Dreifuss/fisiopatología , Mutación , Isoformas de Proteínas/química , Isoformas de Proteínas/genética , Función Ventricular , Distrofia Muscular de Emery-Dreifuss Ligada a X
3.
Int J Cardiovasc Imaging ; 25 Suppl 1: 83-94, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19132544

RESUMEN

This study evaluated arterial wall stiffness independent of variant background blood pressure. A new technique-arterial wall stiffness index (AWSI)-was developed and its use verified. Intraluminal pressure and luminal volume were measured on eight swine descending aortas. AWSI was formulated to evaluate absolute arterial wall stiffness independent of variable blood pressure and aortic size. AWSI variability with pressure change was compared with other wall stiffness evaluation parameters. AWSI determined from 100 descending aortic cine CT images and 108 carotid artery ultrasonography datasets were compared with age and Framingham risk score, respectively. Between 50 and 360 mmHg blood pressures, AWSI variance was 5.43% compared to 64.99% for classical compliance. AWSI correlated better with Framingham risk score and age than conservative wall stiffness evaluation methods. AWSI is a suitable method to evaluate arterial wall properties independent of variable background blood pressure and aortic size effects.


Asunto(s)
Aorta/patología , Enfermedades de la Aorta/patología , Arteria Carótida Común/patología , Adulto , Anciano , Anciano de 80 o más Años , Animales , Aorta/fisiopatología , Enfermedades de la Aorta/diagnóstico por imagen , Enfermedades de la Aorta/fisiopatología , Aortografía/métodos , Presión Sanguínea , Arteria Carótida Común/diagnóstico por imagen , Arteria Carótida Común/fisiopatología , Elasticidad , Estudios de Factibilidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Modelos Animales , Modelos Cardiovasculares , Flujo Pulsátil , Estudios Retrospectivos , Porcinos , Tomografía Computarizada por Rayos X , Ultrasonografía Doppler , Adulto Joven
4.
Circ Cardiovasc Imaging ; 1(1): 23-30, 2008 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19808511

RESUMEN

BACKGROUND: Pulmonary hypertension is a disease characterized by an elevation in pulmonary arterial pressure that is diagnosed invasively via right heart catheterization. Such pathological altered pressures in the pulmonary vascular system should lead to changes in blood flow patterns in the main pulmonary artery. METHODS AND RESULTS: Forty-eight subjects (22 with manifest pulmonary hypertension, 13 with latent pulmonary hypertension, and 13 normal control subjects) underwent time-resolved 3D magnetic resonance phase-contrast imaging of the main pulmonary artery. Velocity fields that resulted from measurements were calculated, visualized, and analyzed with dedicated software. Main findings were as follows: (1) Manifest pulmonary hypertension coincides with the appearance of a vortex of blood flow in the main pulmonary artery (sensitivity and specificity of 1.00, 95% confidence intervals of 0.84 to 1.00 and 0.87 to 1.00, respectively), and (2) the relative period of existence of the vortex correlates significantly with mean pulmonary arterial pressure at rest (correlation coefficient of 0.94). To test the diagnostic performance of the vortex criterion, we furthermore investigated 55 patients in a blinded prospective study (22 with manifest pulmonary hypertension, 32 with latent pulmonary hypertension, and 1 healthy subject), which resulted in a sensitivity of 1.00 and specificity of 0.91 (95% confidence intervals of 0.84 to 1.00 and 0.76 to 0.98, respectively). Comparison of catheter-derived mean pulmonary artery pressure measurements and calculated mean pulmonary artery pressure values resulted in a standard deviation of differences of 3.6 mm Hg. CONCLUSIONS: Vortices of blood flow in the main pulmonary artery enable the identification of manifest pulmonary hypertension. Elevated mean pulmonary arterial pressures can be measured from the period of vortex existence.


Asunto(s)
Presión Sanguínea , Hipertensión Pulmonar/diagnóstico , Angiografía por Resonancia Magnética , Arteria Pulmonar/fisiopatología , Circulación Pulmonar , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Velocidad del Flujo Sanguíneo , Cateterismo Cardíaco , Estudios de Casos y Controles , Femenino , Humanos , Hipertensión Pulmonar/fisiopatología , Imagenología Tridimensional , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Estudios Prospectivos , Flujo Sanguíneo Regional , Sensibilidad y Especificidad , Método Simple Ciego , Adulto Joven
5.
J Thorac Cardiovasc Surg ; 134(1): 23-8, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17599482

RESUMEN

OBJECTIVE: Results of short- and midterm follow-up studies of the patency rate of the Symmetry aortic connector systems (St Jude Medical, Inc, Minneapolis, Minn) are controversial. Long-term follow-up studies are still lacking (so far, the longest mean follow-up period was 19 months). The aim of our study was (1) to evaluate the patency rate of this device over a longer time-period and (2) to analyze risk factors for graft occlusion. METHODS: Between November 2000 and July 2003, 76 Symmetry aortic connector systems were implanted in 42 patients. At follow-up, 24 patients with 44 mechanical connectors were studied with 64-slice cardiac computed tomography. Eight patients had died previously, 6 patients refused to undergo a computed tomographic scan, and 4 patients had to be excluded because of impaired renal function. RESULTS: From a total of 44 mechanical connectors studied, 24 (55%) were occluded, 20 (45%; confidence intervals 31%-61%) were patent, and 7 of these grafts showed stenosis in the area of the connector. Mean follow-up was 41 +/- 10 months (18-52 months). Sex, age, left main stenosis, hyperlipidemia, hypertension, renal failure, target vessel, stenosis of the target vessel, diameter of the target vessel, type of surgical intervention, diabetes, ejection fraction, postoperative anticoagulation regimen, and the connector size showed no significant influence on the bypass graft patency (P > .05). The bypass graft flow was recognized to be the only risk factor for bypass graft occlusion (P = .0256). CONCLUSION: Midterm follow-up data show a high number of occluded Symmetry aortic connector system vein grafts. On the basis of these observations, the use of the connector was abandoned at our institution.


Asunto(s)
Válvula Aórtica/cirugía , Prótesis Vascular/efectos adversos , Procedimientos Quirúrgicos Cardiovasculares/efectos adversos , Puente de Arteria Coronaria/instrumentación , Oclusión de Injerto Vascular/etiología , Anciano , Anciano de 80 o más Años , Anastomosis Quirúrgica/efectos adversos , Aorta/diagnóstico por imagen , Aorta/cirugía , Válvula Aórtica/diagnóstico por imagen , Aortografía , Calcinosis/cirugía , Causas de Muerte , Puente de Arteria Coronaria/métodos , Puente de Arteria Coronaria/mortalidad , Ecocardiografía Transesofágica , Femenino , Estudios de Seguimiento , Oclusión de Injerto Vascular/diagnóstico por imagen , Oclusión de Injerto Vascular/mortalidad , Oclusión de Injerto Vascular/fisiopatología , Oclusión de Injerto Vascular/prevención & control , Humanos , Imagenología Tridimensional , Masculino , Persona de Mediana Edad , Factores de Riesgo , Vena Safena/trasplante , Tomografía Computarizada por Rayos X/métodos , Grado de Desobstrucción Vascular
6.
Curr Pharm Des ; 11(4): 457-75, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15725065

RESUMEN

The clinical role of magnetic resonance in diseases of the heart and great vessels is rapidly evolving. Cardiovascular magnetic resonance (CMR) has become an established non-invasive imaging modality for the assessment of various cardiac disorders, such as congenital heart disease, cardiac masses, cardiomyopathies, aortic and pericardial diseases. Moreover, due to its accuracy and reproducibility, CMR is currently considered the gold standard for quantification of ventricular volumes, function, and mass. Thus, this technique is ideally suited to assess the efficacy of therapeutic interventions on ventricular hypertrophy and remodelling, which may allow a reduction in sample size to show clinically relevant effects. Comprehensive functional assessment is possible by CMR due to its capability to measure flow velocity and flow volume, which is a basic requirement to quantify lesion severity in valvular heart disease. Within the past years, major technical advances have considerably improved acquisition speed and image quality making CMR a useful tool for the evaluation of patients with ischaemic heart disease. Although the clinical robustness of coronary magnetic resonance angiography still needs improvement, CMR currently provides valuable information to detect reversible ischemia, myocardial infarction, and residual viability. In this review we will present in detail the well-established indications of CMR accompanied by an outlook on new applications that are likely to enter the clinical arena in the near future.


Asunto(s)
Enfermedades Cardiovasculares/diagnóstico , Imagen por Resonancia Magnética/métodos , Enfermedades de la Aorta/diagnóstico , Cardiomiopatías/diagnóstico , Enfermedades Cardiovasculares/congénito , Enfermedades Cardiovasculares/fisiopatología , Enfermedad Coronaria/diagnóstico , Neoplasias Cardíacas/diagnóstico , Enfermedades de las Válvulas Cardíacas/diagnóstico , Humanos
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