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Clinical and biological characterization of 20 patients with TANGO2 deficiency indicates novel triggers of metabolic crises and no primary energetic defect.
Bérat, Claire-Marine; Montealegre, Sebastian; Wiedemann, Arnaud; Nuzum, Malou Le Corronc; Blondel, Amélie; Debruge, Hugo; Cano, Aline; Chabrol, Brigitte; Hoebeke, Célia; Polak, Michel; Stoupa, Athanasia; Feillet, François; Torre, Stéphanie; Boddaert, Nathalie; Bruel, Henri; Barth, Magalie; Damaj, Lena; Abi-Wardé, Marie-Thérèse; Afenjar, Alexandra; Benoist, Jean-François; Madrange, Marine; Caccavelli, Laure; Renard, Perrine; Hubas, Arnaud; Nusbaum, Patrick; Pontoizeau, Clément; Gobin, Stéphanie; van Endert, Peter; Ottolenghi, Chris; Maltret, Alice; de Lonlay, Pascale.
Afiliación
  • Bérat CM; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
  • Montealegre S; Université de Paris, Paris, France.
  • Wiedemann A; Reference Center of inherited Metabolic Diseases, Necker-Enfants-Malades University hospital, APHP, Imagine Institute, Filière G2M, Paris, France.
  • Nuzum MLC; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
  • Blondel A; Reference Center of inherited Metabolic Diseases, Necker-Enfants-Malades University hospital, APHP, Imagine Institute, Filière G2M, Paris, France.
  • Debruge H; Department of Pediatric Intensive Care, Reference Center of Inherited Metabolic Disorders, INSERM U1256, Nancy Hospital, Nancy, France.
  • Cano A; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
  • Chabrol B; Department of Biochemistry, Necker-Enfants-Malades University Hospital, APHP, Filière G2M, Paris, France.
  • Hoebeke C; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
  • Polak M; Reference Center of Inherited Metabolic Disorders, La Timone Hospital, Filière G2M, Marseille, France.
  • Stoupa A; Reference Center of Inherited Metabolic Disorders, La Timone Hospital, Filière G2M, Marseille, France.
  • Feillet F; Reference Center of Inherited Metabolic Disorders, La Timone Hospital, Filière G2M, Marseille, France.
  • Torre S; Université de Paris, Paris, France.
  • Boddaert N; Endocrinology Unit, Reference Center of Rare Endocrine Diseases of Growth and Development, Necker-Enfants-Malades, University hospital, APHP, Imagine Institute, Paris, France.
  • Bruel H; Université de Paris, Paris, France.
  • Barth M; Endocrinology Unit, Reference Center of Rare Endocrine Diseases of Growth and Development, Necker-Enfants-Malades, University hospital, APHP, Imagine Institute, Paris, France.
  • Damaj L; Department of Pediatric Intensive Care, Reference Center of Inherited Metabolic Disorders, INSERM U1256, Nancy Hospital, Nancy, France.
  • Abi-Wardé MT; Competence Center of Inherited Metabolic Disorders, Rouen Hospital, Filière G2M, Rouen, France.
  • Afenjar A; Université de Paris, Paris, France.
  • Benoist JF; Paediatric Radiology Department, Necker-Enfants-Malades University hospital, APHP and INSERM U1163, Imagine Institute, Paris, France.
  • Madrange M; Pediatrics Department, Le Havre Hospital, Le Havre, France.
  • Caccavelli L; Pediatrics Department, Angers Hospital, Angers, France.
  • Renard P; Pediatrics Department, Rennes Hospital, Rennes, France.
  • Hubas A; Pediatrics Department, Strasbourg Hospital, Strasbourg, France.
  • Nusbaum P; Reference Center of Cerebellar Malformations and Congenital Diseases, Trousseau Hospital, APHP, Paris, France.
  • Pontoizeau C; Department of Biochemistry, Necker-Enfants-Malades University Hospital, APHP, Filière G2M, Paris, France.
  • Gobin S; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
  • van Endert P; Reference Center of inherited Metabolic Diseases, Necker-Enfants-Malades University hospital, APHP, Imagine Institute, Filière G2M, Paris, France.
  • Ottolenghi C; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
  • Maltret A; Reference Center of inherited Metabolic Diseases, Necker-Enfants-Malades University hospital, APHP, Imagine Institute, Filière G2M, Paris, France.
  • de Lonlay P; Inserm U1151, Institut Necker Enfants-Malades, Paris, France.
J Inherit Metab Dis ; 44(2): 415-425, 2021 03.
Article en En | MEDLINE | ID: mdl-32929747
TANGO2 disease is a severe inherited disorder associating multiple symptoms such as metabolic crises, encephalopathy, cardiac arrhythmias, and hypothyroidism. The mechanism of action of TANGO2 is currently unknown. Here, we describe a cohort of 20 French patients bearing mutations in the TANGO2 gene. We found that the main clinical presentation was the association of neurodevelopmental delay (n = 17), acute metabolic crises (n = 17) and hypothyroidism (n = 12), with a large intrafamilial clinical variability. Metabolic crises included rhabdomyolysis (15/17), neurological symptoms (14/17), and cardiac features (12/17; long QT (n = 10), Brugada pattern (n = 2), cardiac arrhythmia (n = 6)) that required intensive care. We show previously uncharacterized triggers of metabolic crises in TANGO2 patients, such as some anesthetics and possibly l-carnitine. Unexpectedly, plasma acylcarnitines, plasma FGF-21, muscle histology, and mitochondrial spectrometry were mostly normal. Moreover, in patients' primary myoblasts, palmitate and glutamine oxidation rates, and the mitochondrial network were also normal. Finally, we found variable mitochondrial respiration and defective clearance of oxidized DNA upon cycles of starvation and refeeding. We conclude that TANGO2 disease is a life-threatening disease that needs specific cardiac management and anesthesia protocol. Mechanistically, TANGO2 disease is unlikely to originate from a primary mitochondrial defect. Rather, we suggest that mitochondrial defects are secondary to strong extrinsic triggers in TANGO2 deficient patients.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Arritmias Cardíacas / Rabdomiólisis / Translocador Nuclear del Receptor de Aril Hidrocarburo / Trastornos del Neurodesarrollo Tipo de estudio: Guideline / Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Europa Idioma: En Revista: J Inherit Metab Dis Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Arritmias Cardíacas / Rabdomiólisis / Translocador Nuclear del Receptor de Aril Hidrocarburo / Trastornos del Neurodesarrollo Tipo de estudio: Guideline / Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Europa Idioma: En Revista: J Inherit Metab Dis Año: 2021 Tipo del documento: Article País de afiliación: Francia