Successful treatment of infantile-onset ACAD9-related cardiomyopathy with a combination of sodium pyruvate, beta-blocker, and coenzyme Q10.
Acidosis
/ complications
Acyl-CoA Dehydrogenase
/ deficiency
Acyl-CoA Dehydrogenases
/ deficiency
Adrenergic beta-Antagonists
/ administration & dosage
Amino Acid Metabolism, Inborn Errors
/ complications
Cardiomyopathies
/ complications
Cardiomyopathy, Hypertrophic
/ complications
Carvedilol
/ administration & dosage
Drug Therapy, Combination
Female
Humans
Infant, Newborn
Mitochondrial Diseases
/ complications
Muscle Weakness
/ complications
Prognosis
Pyruvates
/ administration & dosage
Ubiquinone
/ administration & dosage
Vitamins
/ administration & dosage
ACAD9
cardiomyopathy
deficiency
mitochondria
pyruvate
treatment
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
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