Literature DB >> 27233227

Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patients.

Joseph P Dewulf1, Catherine Barrea2, Marie-Françoise Vincent1, Corinne De Laet3, Rudy Van Coster4, Sara Seneca5, Sandrine Marie1, Marie-Cécile Nassogne6.   

Abstract

Acyl-CoA dehydrogenase 9 (ACAD9) is a mitochondrial protein involved in oxidative phosphorylation complex I biogenesis. This protein also exhibits acyl-CoA dehydrogenase (ACAD) activity. ACAD9-mutated patients have been reported to suffer from primarily heart, muscle, liver, and nervous system disorders. ACAD9 mutation is suspected in cases of elevated lactic acid levels combined with complex I deficiency, and confirmed by ACAD9 gene analysis. At least 18 ACAD9-mutated patients have previously been reported, usually displaying severe cardiac involvement. We retrospectively studied nine additional patients from three unrelated families with a wide spectrum of cardiac involvement between the families as well as the patients from the same families. All patients exhibited elevated lactate levels. Deleterious ACAD9 mutations were identified in all patients except one for whom it was not possible to recover DNA. To our knowledge, this is one of the first reports on isolated mild ventricular hypertrophy due to ACAD9 mutation in a family with moderate symptoms during adolescence. This report also confirms that dilated cardiomyopathy may occur in conjunction with ACAD9 mutation and that some patients may respond clinically to riboflavin treatment. Of note, several patients suffered from patent ductus arteriosus (PDA), with one exhibiting a complex congenital heart defect. It is yet unknown whether these cardiac manifestations were related to ACAD9 mutation. In conclusion, this disorder should be suspected in the presence of lactic acidosis, complex I deficiency, and any cardiac involvement, even mild.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ACAD9; Acyl-COA dehydrogenase 9; Cardiomyopathy; Complex I deficiency

Mesh:

Substances:

Year:  2016        PMID: 27233227     DOI: 10.1016/j.ymgme.2016.05.005

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  7 in total

1.  Post-mortem genetic investigation in sudden cardiac death victims: complete exon sequencing of forty genes using next-generation sequencing.

Authors:  Jennifer Fadoni; Agostinho Santos; Laura Cainé
Journal:  Int J Legal Med       Date:  2022-01-05       Impact factor: 2.791

2.  Advances in the Understanding and Treatment of Mitochondrial Fatty Acid Oxidation Disorders.

Authors:  Eric S Goetzman
Journal:  Curr Genet Med Rep       Date:  2017-07-25

Review 3.  Dynamics of Human Mitochondrial Complex I Assembly: Implications for Neurodegenerative Diseases.

Authors:  Gabriele Giachin; Romain Bouverot; Samira Acajjaoui; Serena Pantalone; Montserrat Soler-López
Journal:  Front Mol Biosci       Date:  2016-08-22

4.  Mitochondrial multiorgan disorder syndrome (MIMODS) due to a compound heterozygous mutation in the ACAD9 gene.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Mol Genet Metab Rep       Date:  2017-07-28

5.  An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach.

Authors:  H K Aintablian; V Narayanan; N Belnap; K Ramsey; T A Grebe
Journal:  Mol Genet Metab Rep       Date:  2016-12-29

Review 6.  Human diseases associated with defects in assembly of OXPHOS complexes.

Authors:  Daniele Ghezzi; Massimo Zeviani
Journal:  Essays Biochem       Date:  2018-07-20       Impact factor: 8.000

Review 7.  Blackout in the powerhouse: clinical phenotypes associated with defects in the assembly of OXPHOS complexes and the mitoribosome.

Authors:  Daniella H Hock; David R L Robinson; David A Stroud
Journal:  Biochem J       Date:  2020-11-13       Impact factor: 3.857

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.