Aims: Mitochondrial disease (MD) is a genetic disorder affecting skeletal muscles, with possible myocardial disease. The ergoreflex, sensitive to skeletal muscle work, regulates ventilatory and autonomic responses to exercise. We hypothesized the presence of an increased ergoreflex sensitivity in MD patients, its association with abnormal ventilatory and autonomic responses, and possibly with subclinical cardiac involvement. Methods and results: Twenty-five MD patients (aged 46±3 years, 32% male) with skeletal myopathy but without known cardiac disease, underwent a thorough evaluation including BNPs, galectin-3, soluble suppression of tumorigenesis 2 (sST2), high sensitivity troponin T/I, catecholamines, ECG, 24-h ECG recording, cardiopulmo...
Mitochondrial diseases (MD) are a heterogeneous group of rare genetically determined disorders, char...
Myocardial and skeletal muscle high energy phosphate metabolism is abnormal in heart failure, but th...
Background: During aging a mosaic of normal cells and cells with mitochondrial deficiency develops i...
Aims: Mitochondrial disease (MD) is a genetic disorder affecting skeletal muscles, with possible myo...
Background: Previous studies in heart failure with reduced ejection fraction (HFrEF) suggest that s...
CMR, cardiac magnetic resonance; CPK, creatine phosphokinase; ECG, electrocardiogram; hs-cTnT, high ...
The control of ventilation and cardiovascular function during physical activity is partially regulat...
Abstract Objective Mitochondrial DNA mutations are associated with an increased risk of heart diseas...
AbstractBackgroundCardiac hypertrophic remodelling and systolic dysfunction are common in patients w...
The myocardium is among the most energy-consuming tissues in the body, burning from 6 to 30 kg of AT...
PhD ThesisMitochondrial dysfunction occurs in patients with mitochondrial disease, in neurodegenerat...
International audienceKEY POINTS:Ninety-eight per cent of patients with Duchenne muscular dystrophy ...
AbstractAlthough neuromuscular clinical features often dominate the clinical presentation of mitocho...
Histological mitochondrial changes are generally found to be associated with late onset myofibrillar...
Mitochondrial diseases (MD) are a heterogeneous group of rare genetically determined disorders, char...
Myocardial and skeletal muscle high energy phosphate metabolism is abnormal in heart failure, but th...
Background: During aging a mosaic of normal cells and cells with mitochondrial deficiency develops i...
Aims: Mitochondrial disease (MD) is a genetic disorder affecting skeletal muscles, with possible myo...
Background: Previous studies in heart failure with reduced ejection fraction (HFrEF) suggest that s...
CMR, cardiac magnetic resonance; CPK, creatine phosphokinase; ECG, electrocardiogram; hs-cTnT, high ...
The control of ventilation and cardiovascular function during physical activity is partially regulat...
Abstract Objective Mitochondrial DNA mutations are associated with an increased risk of heart diseas...
AbstractBackgroundCardiac hypertrophic remodelling and systolic dysfunction are common in patients w...
The myocardium is among the most energy-consuming tissues in the body, burning from 6 to 30 kg of AT...
PhD ThesisMitochondrial dysfunction occurs in patients with mitochondrial disease, in neurodegenerat...
International audienceKEY POINTS:Ninety-eight per cent of patients with Duchenne muscular dystrophy ...
AbstractAlthough neuromuscular clinical features often dominate the clinical presentation of mitocho...
Histological mitochondrial changes are generally found to be associated with late onset myofibrillar...
Mitochondrial diseases (MD) are a heterogeneous group of rare genetically determined disorders, char...
Myocardial and skeletal muscle high energy phosphate metabolism is abnormal in heart failure, but th...
Background: During aging a mosaic of normal cells and cells with mitochondrial deficiency develops i...