Literature DB >> 28689308

Triheptanoin: A Rescue Therapy for Cardiogenic Shock in Carnitine-acylcarnitine Translocase Deficiency.

Sidharth Mahapatra1, Amitha Ananth2, Nancy Baugh3, Mihaela Damian4, Gregory M Enns5.   

Abstract

Carnitine-acylcarnitine translocase (CACT) deficiency is a rare long-chain fatty acid oxidation disorder (LC-FAOD) with high mortality due to cardiomyopathy or lethal arrhythmia. Triheptanoin (UX007), an investigational drug composed of synthetic medium odd-chain triglycerides, is a novel therapy in development for LC-FAOD patients. However, cases of its safe and efficacious use to reverse severe heart failure in CACT deficiency are limited. Here, we present a detailed report of an infant with CACT deficiency admitted in metabolic crisis that progressed into severe cardiogenic shock who was successfully treated by triheptanoin. The child was managed, thereafter, on triheptanoin until her death at 3 years of age from a cardiopulmonary arrest in the setting of acute respiratory illness superimposed on chronic hypercarbic respiratory failure.

Entities:  

Keywords:  Cardiogenic shock; Carnitine-acylcarnitine translocase deficiency; Long-chain fatty acid oxidation disorder; Triheptanoin; UX007

Year:  2017        PMID: 28689308      PMCID: PMC5953892          DOI: 10.1007/8904_2017_36

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  15 in total

Review 1.  Long-term major clinical outcomes in patients with long chain fatty acid oxidation disorders before and after transition to triheptanoin treatment--A retrospective chart review.

Authors:  Jerry Vockley; Deborah Marsden; Elizabeth McCracken; Stephanie DeWard; Amanda Barone; Kristen Hsu; Emil Kakkis
Journal:  Mol Genet Metab       Date:  2015-06-18       Impact factor: 4.797

2.  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 3.  Carnitine-acylcarnitine translocase deficiency: implications in human pathology.

Authors:  S V Pande; M S Murthy
Journal:  Biochim Biophys Acta       Date:  1994-07-18

4.  Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders.

Authors:  J Vockley; J Charrow; J Ganesh; M Eswara; G A Diaz; E McCracken; R Conway; G M Enns; J Starr; R Wang; J E Abdenur; J Sanchez-de-Toledo; D L Marsden
Journal:  Mol Genet Metab       Date:  2016-08-27       Impact factor: 4.797

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.  Carnitine-acylcarnitine translocase deficiency: experience with four cases in Spain and review of the literature.

Authors:  Isidro Vitoria; Elena Martín-Hernández; Luis Peña-Quintana; María Bueno; Pilar Quijada-Fraile; Jaime Dalmau; Sofia Molina-Marrero; Belén Pérez; Begoña Merinero
Journal:  JIMD Rep       Date:  2015-01-23

7.  Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride.

Authors:  Charles R Roe; Lawrence Sweetman; Diane S Roe; France David; Henri Brunengraber
Journal:  J Clin Invest       Date:  2002-07       Impact factor: 14.808

8.  A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay.

Authors:  Chad R Haldeman-Englert; Xiaowu Gai; Juan Carlos Perin; Melissa Ciano; Sara S Halbach; Elizabeth A Geiger; Donna M McDonald-McGinn; Hakon Hakonarson; Elaine H Zackai; Tamim H Shaikh
Journal:  Eur J Med Genet       Date:  2008-12-13       Impact factor: 2.708

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.  Aberrant mRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiency.

Authors:  B Y Hsu; V Iacobazzi; Z Wang; H Harvie; R A Chalmers; J M Saudubray; F Palmieri; A Ganguly; C A Stanley
Journal:  Mol Genet Metab       Date:  2001 Sep-Oct       Impact factor: 4.797

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  7 in total

1.  Association of Abnormal Serum L-Carnitine Levels with Idiopathic Changes in Left Ventricular Geometry in Pediatric and Adolescent Patients.

Authors:  Mohsen Shahidi; Khaled Rahmani; Abdorrahim Afkhamzadeh
Journal:  Iran J Med Sci       Date:  2022-05

2.  Medium branched chain fatty acids improve the profile of tricarboxylic acid cycle intermediates in mitochondrial fatty acid β-oxidation deficient cells: A comparative study.

Authors:  Anuradha Karunanidhi; Clinton Van't Land; Dhivyaa Rajasundaram; Mateus Grings; Jerry Vockley; Al-Walid Mohsen
Journal:  J Inherit Metab Dis       Date:  2022-02-02       Impact factor: 4.750

Review 3.  Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation: Two case reports and brief literature review.

Authors:  Hui-Ming Yan; Hao Hu; Aisha Ahmed; Bing-Bing Feng; Jing Liu; Zheng-Jun Jia; Hua Wang
Journal:  Medicine (Baltimore)       Date:  2017-11       Impact factor: 1.817

4.  The use of sodium DL-3-Hydroxybutyrate in severe acute neuro-metabolic compromise in patients with inherited ketone body synthetic disorders.

Authors:  Kaustuv Bhattacharya; Walid Matar; Adviye Ayper Tolun; Beena Devanapalli; Sue Thompson; Troy Dalkeith; Kate Lichkus; Michel Tchan
Journal:  Orphanet J Rare Dis       Date:  2020-02-18       Impact factor: 4.123

5.  Bioinformatics identification of potential candidate blood indicators for doxorubicin-induced heart failure.

Authors:  Guo-Xing Wan; Li-Hua Ji; Wen-Bin Xia; Lan Cheng; Yong-Gang Zhang
Journal:  Exp Ther Med       Date:  2018-07-19       Impact factor: 2.447

6.  No effect of triheptanoin on exercise performance in McArdle disease.

Authors:  Karen L Madsen; Pascal Laforêt; Astrid E Buch; Mads G Stemmerik; Chris Ottolenghi; Stéphane N Hatem; Daniel T Raaschou-Pedersen; Nanna S Poulsen; Maria Atencio; Marie-Pierre Luton; Alexandre Ceccaldi; Ronald G Haller; Ros Quinlivan; Fanny Mochel; John Vissing
Journal:  Ann Clin Transl Neurol       Date:  2019-09-14       Impact factor: 4.511

7.  Late-Onset Carnitine-Acylcarnitine Translocase Deficiency With SLC25A20 c.199-10T>G Variation: Case Report and Pathologic Analysis of Liver Biopsy.

Authors:  Min Chen; Yao Cai; Sitao Li; Hui Xiong; Mengxian Liu; Fei Ma; Xin Xiao; Hu Hao
Journal:  Front Pediatr       Date:  2020-10-30       Impact factor: 3.418

  7 in total

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