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Mol Genet Metab. 2015 Jun-Jul;115(2-3):91-4. doi: 10.1016/j.ymgme.2015.04.008. Epub 2015 May 2.

Aromatic L-amino acid decarboxylase deficiency diagnosed by clinical metabolomic profiling of plasma.

Author information

1
Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
2
Section of Pediatric Neurology and Neuroscience, Baylor College of Medicine, Houston, TX, USA.
3
Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA; Section of Pediatric Neurology and Neuroscience, Baylor College of Medicine, Houston, TX, USA.
4
Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA. Electronic address: elsea@bcm.edu.

Abstract

Aromatic L-amino acid decarboxylase (AADC) deficiency is an inborn error of metabolism affecting the biosynthesis of serotonin, dopamine, and catecholamines. We report a case of AADC deficiency that was detected using the Global MAPS platform. This is a novel platform that allows for parallel clinical testing of hundreds of metabolites in a single plasma specimen. It uses a state-of-the-art mass spectrometry platform, and the resulting spectra are compared against a library of ~2500 metabolites. Our patient is now a 4 year old boy initially seen at 11 months of age for developmental delay and hypotonia. Multiple tests had not yielded a diagnosis until exome sequencing revealed compound heterozygous variants of uncertain significance (VUS), c.286G>A (p.G96R) and c.260C>T (p.P87L) in the DDC gene, causal for AADC deficiency. CSF neurotransmitter analysis confirmed the diagnosis with elevated 3-methoxytyrosine (3-O-methyldopa). Metabolomic profiling was performed on plasma and revealed marked elevation in 3-methoxytyrosine (Z-score +6.1) consistent with the diagnosis of AADC deficiency. These results demonstrate that the Global MAPS platform is able to diagnose AADC deficiency from plasma. In summary, we report a novel and less invasive approach to diagnose AADC deficiency using plasma metabolomic profiling.

KEYWORDS:

3-O-methyldopa; 3-methoxytyrosine; Aromatic l-amino acid decarboxylase deficiency; Metabolomic profiling; Oculogyric crisis

PMID:
25956449
DOI:
10.1016/j.ymgme.2015.04.008
[Indexed for MEDLINE]

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