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DOI 10.1016/j.acvd.2021.10.010

Медицинская библиотека · Archives of cardiovascular diseases · 2021

Characterizing cardiac phenotype in Friedreich's ataxia: The CARFA study.

Legrand Lise, Weinsaft Jonathan W, Pousset Francoise, Ewenczyk Claire, Charles Perrine, Hatem Stéphane, Heinzmann Anna, Biet Marie, Durr Alexandra, Redheuil Alban

СтатьяНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Friedreich's ataxia is an autosomal recessive mitochondrial disease caused by a triplet repeat expansion in the frataxin gene (FXN), exhibiting cerebellar sensory ataxia, diabetes and cardiomyopathy. Cardiac complications are the major cause of early death.

AIMS: To characterize the cardiac phenotype associated with Friedreich's ataxia, and to assess the evolution of the associated cardiopathy over 1 year.

METHODS

This observational single-centre open label study consisted of two groups: 20 subjects with Friedreich's ataxia and 20 healthy controls studied over two visits over 1 year. All subjects had transthoracic echocardiography, cardiac magnetic resonance imaging, cardiopulmonary exercise testing, quantification of serum cardiac biomarkers and neurological assessment.

RESULTS

Patients with Friedreich's ataxia had left ventricular hypertrophy, with significantly smaller left ventricular diastolic diameters and volumes and increased wall thicknesses. Cardiac magnetic resonance imaging demonstrated significant concentric left ventricular remodelling, according to the mass/volume ratio, and focal myocardial fibrosis in 50% of patients with Friedreich's ataxia. Cardiopulmonary exercise testing showed alteration of left ventricular diastolic filling in patients with Friedreich's ataxia, with an elevated VE/VCO2 slope (ventilatory flow/exhaled volume of carbon dioxide). High-sensitivity troponin T plasma concentrations were higher in subjects with Friedreich's ataxia. None of the previous variables changed at 1 year. Neurological assessments remained stable for both groups, except for the nine-hole pegboard test, which was altered over 1 year.

CONCLUSIONS

The multivariable characterization of the cardiac phenotype of patients with Friedreich's ataxia was significantly different from controls at baseline. Over 1 year there were no clinically significant changes in patients with Friedreich's ataxia compared with healthy controls, whereas the neurological severity score increased modestly.

Для цитирования: Legrand Lise, Weinsaft Jonathan W, Pousset Francoise, Ewenczyk Claire, Charles Perrine, Hatem Stéphane, Heinzmann Anna, Biet Marie, Durr Alexandra, Redheuil Alban. Characterizing cardiac phenotype in Friedreich's ataxia: The CARFA study.. Archives of cardiovascular diseases. 2021. DOI: 10.1016/j.acvd.2021.10.010.

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