Literature DB >> 30401918

Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency.

Kenji Yamada1, Takeshi Taketani2.   

Abstract

Mitochondrial fatty acid oxidation disorders (FAODs) are caused by defects in β-oxidation enzymes, including very long-chain acyl-CoA dehydrogenase (VLCAD), trifunctional protein (TFP), carnitine palmitoyltransferase-2 (CPT2), carnitine-acylcarnitine translocase (CACT) and others. During prolonged fasting, infection, or exercise, patients with FAODs present with hypoglycemia, rhabdomyolysis, cardiomyopathy, liver dysfunction, and occasionally sudden death. This article describes the diagnosis, newborn screening, and treatment of long-chain FAODs with a focus on VLCAD deficiency. VLCAD deficiency is generally classified into three phenotypes based on onset time, but the classification should be comprehensively determined based on genotype, residual enzyme activity, and clinical course, due to a lack of apparent genotype-phenotype correlation. With the expansion of newborn screening for FAODs, several issues have arisen, such as missed detection, overdiagnosis (including detection of benign/asymptomatic type), and poor prognosis of the neonatal-onset form. Meanwhile, dietary management and restriction of exercise have been unnecessary for patients with the benign/asymptomatic type of VLCAD deficiency with a high fatty acid oxidation flux score. Although L-carnitine therapy for VLCAD/TFP deficiency has been controversial, supplementation with L-carnitine may be accepted for CPT2/CACT and multiple acyl-CoA dehydrogenase deficiencies. Recently, a double-blind, randomized controlled trial of triheptanoin (seven-carbon fatty acid triglyceride) versus trioctanoin (regular medium-chain triglyceride) was conducted and demonstrated improvement of cardiac functions on triheptanoin. Additionally, although the clinical efficacy of bezafibrate remains controversial, a recent open-label clinical trial showed efficacy of this drug in improving quality of life. These drugs may be promising for the treatment of FAODs, though further studies are required.

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Year:  2018        PMID: 30401918     DOI: 10.1038/s10038-018-0527-7

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  100 in total

1.  Quantitative plasma acylcarnitine analysis using electrospray tandem mass spectrometry for the diagnosis of organic acidaemias and fatty acid oxidation defects.

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Journal:  J Inherit Metab Dis       Date:  1999-05       Impact factor: 4.982

2.  A novel mutation of late-onset very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Rachel Straussberg; Arnold W Strauss
Journal:  Pediatr Neurol       Date:  2002-08       Impact factor: 3.372

3.  Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.

Authors:  D Bonnet; D Martin; E Villain; P Jouvet; D Rabier; M Brivet; J M Saudubray
Journal:  Circulation       Date:  1999-11-30       Impact factor: 29.690

4.  A method for quantitative acylcarnitine profiling in human skin fibroblasts using unlabelled palmitic acid: diagnosis of fatty acid oxidation disorders and differentiation between biochemical phenotypes of MCAD deficiency.

Authors:  Jürgen G Okun; Stefan Kölker; Andreas Schulze; Dirk Kohlmüller; Katharina Olgemöller; Martin Lindner; Georg F Hoffmann; Ronald J A Wanders; Ertan Mayatepek
Journal:  Biochim Biophys Acta       Date:  2002-10-10

5.  Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death.

Authors:  A Mathur; H F Sims; D Gopalakrishnan; B Gibson; P Rinaldo; J Vockley; G Hug; A W Strauss
Journal:  Circulation       Date:  1999-03-16       Impact factor: 29.690

6.  MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Ute Spiekerkoetter; Bin Sun; Thomas Zytkovicz; Ronald Wanders; Arnold W Strauss; Udo Wendel
Journal:  J Pediatr       Date:  2003-09       Impact factor: 4.406

Review 7.  Treatment of carnitine deficiency.

Authors:  S C Winter
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8.  Screening newborns for inborn errors of metabolism by tandem mass spectrometry.

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Journal:  N Engl J Med       Date:  2003-06-05       Impact factor: 91.245

9.  Selective screening for fatty acid oxidation disorders by tandem mass spectrometry: difficulties in practical discrimination.

Authors:  Yosuke Shigematsu; Satoko Hirano; Ikue Hata; Yukie Tanaka; Masakatsu Sudo; Tsuyoshi Tajima; Nobuo Sakura; Seiji Yamaguchi; Masaki Takayanagi
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2003-07-15       Impact factor: 3.205

10.  A new diagnostic test for VLCAD deficiency using immunohistochemistry.

Authors:  Y Ohashi; Y Hasegawa; K Murayama; M Ogawa; T Hasegawa; M Kawai; N Sakata; K Yoshida; H Yarita; K Imai; I Kumagai; K Murakami; H Hasegawa; S Noguchi; I Nonaka; S Yamaguchi; I Nishino
Journal:  Neurology       Date:  2004-06-22       Impact factor: 9.910

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Review 2.  Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies.

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Journal:  Cells       Date:  2019-03-28       Impact factor: 6.600

3.  Very long-chain acyl-CoA dehydrogenase deficiency nomenclature: compound heterozygosity.

Authors:  Carly M Senefeld; Jonathon W Senefeld
Journal:  J Hum Genet       Date:  2020-01-27       Impact factor: 3.172

4.  The common K333Q polymorphism in long-chain acyl-CoA dehydrogenase (LCAD) reduces enzyme stability and function.

Authors:  Megan E Beck; Yuxun Zhang; Sivakama S Bharathi; Beata Kosmider; Karim Bahmed; Mary K Dahmer; Lawrence M Nogee; Eric S Goetzman
Journal:  Mol Genet Metab       Date:  2020-05-01       Impact factor: 4.797

5.  AAV9 gene replacement therapy for respiratory insufficiency in very-long chain acyl-CoA dehydrogenase deficiency.

Authors:  Marina Zieger; Allison M Keeler; Terence R Flotte; Mai K ElMallah
Journal:  J Inherit Metab Dis       Date:  2019-05-03       Impact factor: 4.982

Review 6.  Targeting adaptive cellular responses to mitochondrial bioenergetic deficiencies in human disease.

Authors:  Christopher F Bennett; Conor T Ronayne; Pere Puigserver
Journal:  FEBS J       Date:  2021-09-12       Impact factor: 5.542

7.  Expert consensus on diagnosis and treatment of very long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Division of Biochemistry and Metabolism Medical Genetics Branch, Chinese Medical Association; Division of Genetics and Metabolism, Child Diseases and Health Care Branch Chinese Association for Maternal and Child Health
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2022-02-25

8.  Notoginsenoside R1 Regulates Ischemic Myocardial Lipid Metabolism by Activating the AKT/mTOR Signaling Pathway.

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Journal:  Front Pharmacol       Date:  2022-06-22       Impact factor: 5.988

Review 9.  Evidence that Oxidative Disbalance and Mitochondrial Dysfunction are Involved in the Pathophysiology of Fatty Acid Oxidation Disorders.

Authors:  Graziela Schmitt Ribas; Carmen Regla Vargas
Journal:  Cell Mol Neurobiol       Date:  2020-09-02       Impact factor: 5.046

10.  Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD).

Authors:  Abbe N Vallejo; Henry J Mroczkowski; Joshua J Michel; Michael Woolford; Harry C Blair; Patricia Griffin; Elizabeth McCracken; Stephanie J Mihalik; Miguel Reyes-Mugica; Jerry Vockley
Journal:  Clin Transl Immunology       Date:  2021-06-27
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