Journal
JOURNAL OF INHERITED METABOLIC DISEASE
Volume 44, Issue 4, Pages 792-808Publisher
WILEY
DOI: 10.1002/jimd.12402
Keywords
AGC1; AGC2; GOT2; inborn metabolic disorder; malate aspartate shuttle; MDH1; MDH2; NAD(H); redox
Funding
- Metakids [2017-075]
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The malate aspartate shuttle (MAS) is crucial for mitochondrial respiration and maintaining cytosolic redox balance, playing a key role in sustaining metabolic pathways like glycolysis and serine biosynthesis. Five potential MAS deficiencies have been reported, mostly presenting with infantile epileptic encephalopathy. Biochemical characteristics such as high lactate, disturbed redox balance, and low serine can aid in diagnosis, while treatment options include a ketogenic diet, serine, and vitamin B6 supplementation.
Over the last few years, various inborn disorders have been reported in the malate aspartate shuttle (MAS). The MAS consists of four metabolic enzymes and two transporters, one of them having two isoforms that are expressed in different tissues. Together they form a biochemical pathway that shuttles electrons from the cytosol into mitochondria, as the inner mitochondrial membrane is impermeable to the electron carrier NADH. By shuttling NADH across the mitochondrial membrane in the form of a reduced metabolite (malate), the MAS plays an important role in mitochondrial respiration. In addition, the MAS maintains the cytosolic NAD(+)/NADH redox balance, by using redox reactions for the transfer of electrons. This explains why the MAS is also important in sustaining cytosolic redox-dependent metabolic pathways, such as glycolysis and serine biosynthesis. The current review provides insights into the clinical and biochemical characteristics of MAS deficiencies. To date, five out of seven potential MAS deficiencies have been reported. Most of them present with a clinical phenotype of infantile epileptic encephalopathy. Although not specific, biochemical characteristics include high lactate, high glycerol 3-phosphate, a disturbed redox balance, TCA abnormalities, high ammonia, and low serine, which may be helpful in reaching a diagnosis in patients with an infantile epileptic encephalopathy. Current implications for treatment include a ketogenic diet, as well as serine and vitamin B6 supplementation.
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