Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome

doi:10.1136/jnnp-2019-321694

. 2020 Apr;91(4):444-445.

doi: 10.1136/jnnp-2019-321694. Epub 2019 Nov 6.

Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome

Elodie Hainque^{1

2}, Aurélie Meneret^{1

2}, Domitille Gras³, Mariana Atencio¹, Marie-Pierre Luton¹, Magali Barbier¹, Anne De Saint Martin⁴, Thierry Billette de Villemeur⁵, Chris Ottolenghi⁶, Emmanuel Roze^{1

2}, Fanny Mochel^{7

8}

Affiliations

¹ Faculté de Médecine de Sorbonne Université, UMR S 1127, Inserm U 1127, and CNRS UMR 7225, and Institut du Cerveau et de la Moelle épinière, Paris, France.
² APHP, Hôpital Pitié-Salpêtrière, Département de Neurologie, Paris, France.
³ APHP, Hôpital Robert Debré, Service de Neurologie pédiatrique, Paris, France.
⁴ CHU de Strasbourg, Hôpital de Hautepierre, Département de Neuropédiatrie, Strasbourg, France.
⁵ APHP, Hôpital Armand Trousseau, Département de Neuropédiatrie, Paris, France.
⁶ APHP et Université Paris Descartes, Explorations Fonctionnelles Métabolomiques, Département de Biologie, Hôpital Necker-Enfants Malades, Paris, France.
⁷ Faculté de Médecine de Sorbonne Université, UMR S 1127, Inserm U 1127, and CNRS UMR 7225, and Institut du Cerveau et de la Moelle épinière, Paris, France fanny.mochel@upmc.fr.
⁸ APHP, Hôpital Pitié-Salpêtrière, Département de Génétique, Paris, France.

PMID: 31694879
DOI: 10.1136/jnnp-2019-321694

Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome

Elodie Hainque et al. J Neurol Neurosurg Psychiatry. 2020 Apr.

. 2020 Apr;91(4):444-445.

doi: 10.1136/jnnp-2019-321694. Epub 2019 Nov 6.

Authors

Affiliations

¹ Faculté de Médecine de Sorbonne Université, UMR S 1127, Inserm U 1127, and CNRS UMR 7225, and Institut du Cerveau et de la Moelle épinière, Paris, France.
² APHP, Hôpital Pitié-Salpêtrière, Département de Neurologie, Paris, France.
³ APHP, Hôpital Robert Debré, Service de Neurologie pédiatrique, Paris, France.
⁴ CHU de Strasbourg, Hôpital de Hautepierre, Département de Neuropédiatrie, Strasbourg, France.
⁵ APHP, Hôpital Armand Trousseau, Département de Neuropédiatrie, Paris, France.
⁶ APHP et Université Paris Descartes, Explorations Fonctionnelles Métabolomiques, Département de Biologie, Hôpital Necker-Enfants Malades, Paris, France.
⁷ Faculté de Médecine de Sorbonne Université, UMR S 1127, Inserm U 1127, and CNRS UMR 7225, and Institut du Cerveau et de la Moelle épinière, Paris, France fanny.mochel@upmc.fr.
⁸ APHP, Hôpital Pitié-Salpêtrière, Département de Génétique, Paris, France.

PMID: 31694879
DOI: 10.1136/jnnp-2019-321694

No abstract available

Keywords: metabolic disease; movement disorders.

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Conflict of interest statement

Competing interests: FM has a patent on the use of triheptanoin in GLUT1-DS (WO2014093901), which has been issued. AM reports non-financial support from ABBVIE, outside the submitted work. ER reports grants, personal fees and non-financial support from Orkyn, grants, personal fees and non-financial support from Aguettant, grants, personal fees and non-financial support from Merz pharma, grants from Ipsen, personal fees from Medday pharma, personal fees from Retrophin, grants and non-financial support from Elivie, grants from Fondation Desmarest, grants from Fonds de dotation Brou de Laurière, grants from Agence Nationale de la Recherche, grants from AMADYS, grants, personal fees and non-financial support from Everpharma, personal fees and non-financial support from Movement Disorders Society, personal fees from European Academy of Neurology, personal fees from International Association of Parkinsonism and related Disorders, non-financial support from Merck, non-financial support from Dystonia Coalition, non-financial support from Dystonia Medical Research Foundation, outside the submitted work.

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Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome

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Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome

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