Literature DB >> 33446227

Long-term experience with triheptanoin in 12 Austrian patients with long-chain fatty acid oxidation disorders.

Sabine Scholl-Bürgi1, Daniela Karall2, Thomas Zöggeler1, Katharina Stock3, Monika Jörg-Streller1, Johannes Spenger4, Vassiliki Konstantopoulou5, Miriam Hufgard-Leitner6.   

Abstract

BACKGROUND: Long-chain fatty acid oxidation disorders (LC-FAOD) are a group of rare inborn errors of metabolism with autosomal recessive inheritance that may cause life-threatening events. Treatment with triheptanoin, a synthetic seven-carbon fatty acid triglyceride compound with an anaplerotic effect, seems beneficial, but clinical experience is limited. We report our long-term experience in an Austrian cohort of LC-FAOD patients.
METHODS: We retrospectively assessed clinical outcome and total hospitalization days per year before and after start with triheptanoin by reviewing medical records of 12 Austrian LC-FAOD patients
RESULTS: For 12 Austrian LC-FAOD patients at three metabolic centers, triheptanoin was started shortly after birth in 3/12, and between 7.34 and 353.3 (median 44.5; mean 81.1) months of age in 9/12 patients. For 11 pediatric patients, mean duration of triheptanoin intake was 5.3 (median 3.9, range 1.2-15.7) years, 10/11 pediatric patients have an ongoing intake of triheptanoin. One patient quit therapy due to reported side effects. Total hospitalization days per year compared to before triheptanoin treatment decreased by 82.3% from 27.1 (range 11-65) days per year to 4.8 (range 0-13) days per year, and hospitalization days in the one year pre- compared to the one year post-triheptanoin decreased by 69.8% from 27.1 (range 4-75) days to 8.2 (range 0-25) days. All patients are in good clinical condition, show normal psychomotor development and no impairment in daily life activities.
CONCLUSION: In this retrospective observational study in an Austrian LC-FAOD cohort, triheptanoin data show improvement in disease course. Triheptanoin appears to be a safe and beneficial treatment option in LC-FAOD. For further clarification, additional prospective randomized controlled trials are needed.

Entities:  

Keywords:  Anaplerotic effect; Fat intake regimen; Inborn errors of metabolism; Inherited metabolic disorders; Long-chain ß-oxidation disorders

Mesh:

Substances:

Year:  2021        PMID: 33446227      PMCID: PMC7807521          DOI: 10.1186/s13023-020-01635-x

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  16 in total

1.  Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop.

Authors:  U Spiekerkoetter; M Lindner; R Santer; M Grotzke; M R Baumgartner; H Boehles; A Das; C Haase; J B Hennermann; D Karall; H de Klerk; I Knerr; H G Koch; B Plecko; W Röschinger; K O Schwab; D Scheible; F A Wijburg; J Zschocke; E Mayatepek; U Wendel
Journal:  J Inherit Metab Dis       Date:  2009-04-28       Impact factor: 4.982

2.  Results from a 78-week, single-arm, open-label phase 2 study to evaluate UX007 in pediatric and adult patients with severe long-chain fatty acid oxidation disorders (LC-FAOD).

Authors:  Jerry Vockley; Barbara Burton; Gerard T Berry; Nicola Longo; John Phillips; Amarilis Sanchez-Valle; Pranoot Tanpaiboon; Stephanie Grunewald; Elaine Murphy; Alexandra Bowden; Wencong Chen; Chao-Yin Chen; Jason Cataldo; Deborah Marsden; Emil Kakkis
Journal:  J Inherit Metab Dis       Date:  2019-01       Impact factor: 4.982

3.  UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24weeks of treatment.

Authors:  J Vockley; B Burton; G T Berry; N Longo; J Phillips; A Sanchez-Valle; P Tanpaiboon; S Grunewald; E Murphy; R Humphrey; J Mayhew; A Bowden; L Zhang; J Cataldo; D L Marsden; E Kakkis
Journal:  Mol Genet Metab       Date:  2017-02-07       Impact factor: 4.797

Review 4.  Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening.

Authors:  Ute Spiekerkoetter
Journal:  J Inherit Metab Dis       Date:  2010-05-07       Impact factor: 4.982

Review 5.  Anaplerotic diet therapy in inherited metabolic disease: therapeutic potential.

Authors:  Charles R Roe; Fanny Mochel
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

6.  Heptanoate as a neural fuel: energetic and neurotransmitter precursors in normal and glucose transporter I-deficient (G1D) brain.

Authors:  Isaac Marin-Valencia; Levi B Good; Qian Ma; Craig R Malloy; Juan M Pascual
Journal:  J Cereb Blood Flow Metab       Date:  2012-10-17       Impact factor: 6.200

7.  Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.

Authors:  U Spiekerkoetter; M Lindner; R Santer; M Grotzke; M R Baumgartner; H Boehles; A Das; C Haase; J B Hennermann; D Karall; H de Klerk; I Knerr; H G Koch; B Plecko; W Röschinger; K O Schwab; D Scheible; F A Wijburg; J Zschocke; E Mayatepek; U Wendel
Journal:  J Inherit Metab Dis       Date:  2009-04-29       Impact factor: 4.982

8.  Carnitine palmitoyltransferase II deficiency: successful anaplerotic diet therapy.

Authors:  C R Roe; B-Z Yang; H Brunengraber; D S Roe; M Wallace; B K Garritson
Journal:  Neurology       Date:  2008-07-22       Impact factor: 9.910

9.  Anaplerotic treatment of long-chain fat oxidation disorders with triheptanoin: Review of 15 years Experience.

Authors:  Charles R Roe; Henri Brunengraber
Journal:  Mol Genet Metab       Date:  2015-10-24       Impact factor: 4.797

10.  Fatal pitfalls in newborn screening for mitochondrial trifunctional protein (MTP)/long-chain 3-Hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.

Authors:  Amelie S Lotz-Havla; Wulf Röschinger; Katharina Schiergens; Katharina Singer; Daniela Karall; Vassiliki Konstantopoulou; Saskia B Wortmann; Esther M Maier
Journal:  Orphanet J Rare Dis       Date:  2018-07-20       Impact factor: 4.123

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  2 in total

1.  Genetic, biochemical, and clinical spectrum of patients with mitochondrial trifunctional protein deficiency identified after the introduction of newborn screening in the Netherlands.

Authors:  Marit Schwantje; Sabine A Fuchs; Lonneke de Boer; Annet M Bosch; Inge Cuppen; Eugenie Dekkers; Terry G J Derks; Sacha Ferdinandusse; Lodewijk Ijlst; Riekelt H Houtkooper; Rose Maase; W Ludo van der Pol; Maaike C de Vries; Rendelien K Verschoof-Puite; Ronald J A Wanders; Monique Williams; Frits Wijburg; Gepke Visser
Journal:  J Inherit Metab Dis       Date:  2022-04-19       Impact factor: 4.750

2.  The Pharmacokinetics of Triheptanoin and Its Metabolites in Healthy Subjects and Patients With Long-Chain Fatty Acid Oxidation Disorders.

Authors:  Sun Ku Lee; Manju Gupta; Jack Shi; Kathleen McKeever
Journal:  Clin Pharmacol Drug Dev       Date:  2021-03-31
  2 in total

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