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No effect of triheptanoin in patients with phosphofructokinase deficiency.
Raaschou-Pedersen, Daniel Emil; Madsen, Karen Lindhardt; Løkken, Nicoline; Storgaard, Jesper Helbo; Quinlivan, Ros; Laforêt, Pascal; Lund, Allan; Van Hall, Gerrit; Vissing, John; Ørngreen, Mette.
Afiliação
  • Raaschou-Pedersen DE; Copenhagen Neuromuscular Center, Copenhagen University Hospital, Copenhagen, Denmark. Electronic address: Daniel.raaschou@gmail.com.
  • Madsen KL; Copenhagen Neuromuscular Center, Copenhagen University Hospital, Copenhagen, Denmark.
  • Løkken N; Copenhagen Neuromuscular Center, Copenhagen University Hospital, Copenhagen, Denmark.
  • Storgaard JH; Copenhagen Neuromuscular Center, Copenhagen University Hospital, Copenhagen, Denmark.
  • Quinlivan R; MRC Centre for Neuromuscular Diseases, National Hospital for Neurology and Neurosurgery, Queen Square, London, England UK.
  • Laforêt P; Neurology Department, Nord/Est/Ile de France neuromuscular center, Raymond-Poincaré Hospital, INSERM U1179, END-ICAP, Versailles Saint-Quentin-en-Yvelines University, Montigny-le-Bretonneux, Garches, France.
  • Lund A; Center for Inherited Metabolic Diseases, Departments of Pediatrics and Clinical Genetics, Copenhagen University Hospital, Copenhagen, Denmark.
  • Van Hall G; Clinical Metabolomics Core Facility, Clinical Biochemistry, Copenhagen. University Hospital & Department of Biomedical Sciences, Faculty of Health & Medical Sciences University of Copenhagen, Copenhagen Denmark.
  • Vissing J; Copenhagen Neuromuscular Center, Copenhagen University Hospital, Copenhagen, Denmark.
  • Ørngreen M; Copenhagen Neuromuscular Center, Copenhagen University Hospital, Copenhagen, Denmark; Center for Inherited Metabolic Diseases, Departments of Pediatrics and Clinical Genetics, Copenhagen University Hospital, Copenhagen, Denmark.
Neuromuscul Disord ; 32(4): 295-304, 2022 04.
Article em En | MEDLINE | ID: mdl-35241345
Phosphofructokinase deficiency (PFKD) is a rare disorder of glycogen metabolism. The lack of phosphofructokinase activity blocks the oxidative pathway from glucose and glycogen to pyruvate. Patients suffer from myopathy, exercise intolerance, and myoglobinuria. Currently, there is no specific treatment for PFKD. We hypothesized that 2 weeks treatment with triheptanoin could improve oxidative metabolism during exercise by bypassing the blocked pyruvate generation in PFKD. The study was a randomized, double-blind, placebo-controlled crossover study. Three genetically verified patients completed two treatment periods of 14 days each with triheptanoin (0.3-1 g × kg-1 × day-1) or placebo liquid. Primary outcomes were heart rate, fatty acid and total oxidation measured via stable isotope and indirect calorimetry methodology during submaximal exercise. Triheptanoin did not improve the primary outcome heart rate during submaximal exercise compared to placebo. Palmitate oxidation was increased during submaximal exercise in one patient but did not increase in the two other patients during triheptanoin treatment. Palmitate production and palmitate utilization increased during exercise and increased to a greater extent with triheptanoin treatment in all three patients. This study suggests that triheptanoin treatment has no effect on heart rate or exercise performance despite increased palmitate production and utilization in patients with PFKD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Palmitatos / Glicogênio Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Palmitatos / Glicogênio Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article