Successful treatment of infantile-onset ACAD9-related cardiomyopathy with a combination of sodium pyruvate, beta-blocker, and coenzyme Q10.


Journal

Journal of pediatric endocrinology & metabolism : JPEM
ISSN: 2191-0251
Titre abrégé: J Pediatr Endocrinol Metab
Pays: Germany
ID NLM: 9508900

Informations de publication

Date de publication:
25 Oct 2019
Historique:
received: 07 05 2019
accepted: 16 07 2019
pubmed: 2 9 2019
medline: 4 3 2020
entrez: 2 9 2019
Statut: ppublish

Résumé

Mitochondrial acyl-CoA dehydrogenase 9 (ACAD9) deficiency is one of the common causes of respiratory chain complex I deficiency, which is characterized by cardiomyopathy, lactic acidemia, and muscle weakness. Infantile cardiomyopathy is the most common phenotype and is usually lethal by the age of 5 years. Riboflavin treatment is known to be effective in ~65% of the patients; however, the remaining are unresponsive to riboflavin and are in need of additional treatment measures. In this report, we describe a patient with ACAD9 deficiency who developed progressive cardiomyopathy at 8 months of age. As the patient's left ventricular ejection fraction (LVEF) kept decreasing to 45.4% at 1 year 8 months, sodium pyruvate treatment was introduced together with a beta-blocker and coenzyme Q10. This resulted in a steady improvement, with full and sustained normalization of cardiac function without riboflavin. The therapy, therefore, might be a useful addition for the treatment of ACAD9 deficiency.

Identifiants

pubmed: 31473688
doi: 10.1515/jpem-2019-0205
pii: /j/jpem.ahead-of-print/jpem-2019-0205/jpem-2019-0205.xml
doi:
pii:

Substances chimiques

Adrenergic beta-Antagonists 0
Pyruvates 0
Vitamins 0
Carvedilol 0K47UL67F2
Ubiquinone 1339-63-5
Acyl-CoA Dehydrogenases EC 1.3.-
Acyl-CoA Dehydrogenase EC 1.3.8.7
ACAD9 protein, human EC 1.3.99.-
coenzyme Q10 EJ27X76M46

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

1181-1185

Auteurs

Takumi Kadoya (T)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Azumi Sakakibara (A)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Kana Kitayama (K)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Yuki Yamada (Y)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Shinji Higuchi (S)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Rie Kawakita (R)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.
Department of Genetic Medicine, Osaka City General Hospital, Osaka, Japan.

Yuki Kawasaki (Y)

Division of Pediatric Cardiology, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Mitsuhiro Fujino (M)

Division of Pediatric Cardiology, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Yosuke Murakami (Y)

Division of Pediatric Cardiology, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Masaru Shimura (M)

Center for Medical Genetics and Division of Metabolism, Chiba Children's Hospital, Chiba, Japan.

Kei Murayama (K)

Center for Medical Genetics and Division of Metabolism, Chiba Children's Hospital, Chiba, Japan.

Akira Ohtake (A)

Department of Pediatrics, Faculty of Medicine, Saitama Medical University, Saitama, Japan.
Center for Intractable Diseases, Saitama Medical University Hospital, Saitama, Japan.

Yasushi Okazaki (Y)

Diagnostics and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Yasutoshi Koga (Y)

Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Japan.

Tohru Yorifuji (T)

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.
Department of Genetic Medicine, Osaka City General Hospital, Osaka, Japan.

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Classifications MeSH