Treatment is guided by the regular monitoring of plasma amino acid concentrations. Patients may also be supplemented with BCAA-free amino acid formula and/or medical meals, to provide non-BCAAs and enable protein synthesis. This is achieved by the restriction of dietary leucine and the careful manipulation of calorie intake to avoid catabolism.
The management of MSUD is centred upon avoiding the toxic accumulation of BCAAs. In severe cases, dialysis may be required to eliminate toxic metabolites. The goal of acute management is to promote protein anabolism and avoid catabolism by giving IV 10% dextrose/0.45% saline. Treatment of neonates with classic MSUD is a medical emergency. Prenatal or preimplantation genetic diagnosis requires the pathogenic variant in both parents to be identified. Families with an affected child should be referred for genetic counselling this is particularly important in families where consanguineous marriage is customary, as there may be implications for the wider family. Affected individuals are always homozygous, or compound heterozygous for pathogenic variants in the same gene. Variants in the BCKDHB and DBT genes, which encode E1b and E2 respectively, are more common in the milder variant forms. In classic MSUD variants in the BCKDHA gene, encoding the E1a subunit, predominate. Variants in the genes that encode three out of the four subunits of BCKAD can cause MSUD. BCKAD is comprised of four subunits (E1a, E1b, E2 and E3), and is the enzyme responsible for the second step in the catabolic pathway for the branched-chain amino acids (leucine, isoleucine and valine). MSUD is an autosomal recessive disorder caused by decreased activity of the branched-chain alpha-ketoacid dehydrogenase complex (BCKAD). This analysis is part of the NHS newborn blood spot screening (NBS) programme in England. MSUD may also be diagnosed by tandem mass-spectrometry analysis of leucine in dried blood spots, as part of a newborn screening programme. Organic acid analysis is used to support the diagnosis by identifying elevated branched-chain keto- and hydroxy-acids in the urine. An elevated plasma allo-isoleucine concentration is diagnostic for MSUD. Isoleucine and valine are typically also elevated, but may be normal or low. In MSUD patients, amino acid analysis is used to detect the characteristic elevation in plasma leucine concentrations. Biochemical testing for the diagnosis of MSUD includes quantitative plasma amino acid and urine organic acid analysis, typically performed by specialist metabolic laboratories. Periods of severe catabolic stress in individuals diagnosed with MSUD can precipitate acute leucine intoxication, leading to vomiting, ataxia and altered consciousness in toddlers and hyperactivity, hallucinations and ataxia in children and adults. Older children typically present with learning difficulties. Affected infants may suffer from developmental delay, feeding problems and poor growth. Milder variant forms of MSUD present later, between the early months and early years of infancy. If left untreated, progressive encephalopathy (manifesting as intermittent apnoea and stereotyped movements, such as ‘fencing’ and ‘bicycling’), may develop, and can ultimately lead to coma and central respiratory failure. Classic MSUD presents soon after birth with poor feeding, vomiting and drowsiness. Milder variant forms also exist, and these typically present later in infancy or childhood. The most common and severe form of the disease is the classic type that presents soon after birth. 
Approximately 1 in 116,000 infants are affected by the condition in the UK. 
MSUD gets its name from the characteristic odour of affected individuals’ urine.Maple syrup urine disease (MSUD) is an autosomal recessive disorder that prevents the body from metabolising the branched-chain amino acids: leucine, isoleucine and valine.
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