Expert Opinion on Orphan Drugs published ‘The potential role of gut microbiota and its modulators in the management of propionic and methylmalonic acidemia’ .
Propionic and methylmalonic acidemia (PA/MMA) are rare inborn errors of metabolism. In PA and MMA propionyl-CoA and/or methylmalonyl- CoA and their derived metabolites build up in the bloodstream. This in turn causes an accumulation of dangerous acids and toxins, which can cause damage to the organs.
In order to manage this accumulation, PA/MMA patients need intensive life-long management. Despite best available clinical practice1Baumgartner MR, et al: Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. Orphanet J Rare Dis . Published on 2014;9:130 ,2Sutton VR, et al: Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. Published on 2012;105:26-33 long-term survivors face multiple complications, such as life-threatening episodes of hyperammonemia and metabolic acidosis3Aldubayan SH, Rodan LH, Berry GT, Levy HL: Acute illness protocol for organic acidemias: methylmalonic acidemia and propionic acidemia. Pediatr Emerg Care. Published on 2017;33:142-146 ,4Kolker S, et al: . The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. J Inherit Metab Dis. Published on 2015;38:1041-1057 intellectual disability, poor growth, movement disorders, epilepsy and autism5Sutton VR, et al: Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. Published on 2012;105:26-33 ,6Fraser JL, Venditti CP, :Methylmalonic and propionic acidemias: clinical management update. Curr Opin Pediatr . Published on 2016;28:682-693 ,7Pena L, Burton BK, :Survey of health status and complications among propionic acidemia patients. Am J Med Genet A . Published on 2012;158A:1641-1646 ,8Kolker S, et al: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype. J Inherit Metab Dis. Published on 2015;38:1059-1074
Gut contribution to total propionate burden in PA/MMA
Propionate, precursor of propionyl-CoA, derives from catabolism of amino acids and lipids but is also one of the main short chain fatty acids produced by gut microbiota.9Thompson GN, Walter JH, Bresson JL, Ford GC, Lyonnet SL, Chalmers RA, Saudubray JM, Leonard JV, Halliday D, (1990): Sources of propionate in inborn errors of propionate metabolism. Metabolism. … Continue reading The gut microbiota is responsible for an estimated 25% of the total propionate production. Using stable isotope techniques to measure propionate production in patients with PA/MMA, the relative contributions of amino acids, lipids and gut microbiota are estimated as 50%, 25%, and 25%.10Thompson GN, Walter JH, Bresson JL, Ford GC, Lyonnet SL, Chalmers RA, Saudubray JM, Leonard JV, Halliday D, (1990): Sources of propionate in inborn errors of propionate metabolism. Metabolism. … Continue reading,11Leonard JV, Stable isotope studies in propionic and methylmalonic acidaemia. Eur J Pediatr. Published on 1997;156 Suppl 1:S67-9
The potential role of gut microbiota as a source of propionate production provides a potentially modifiable target. In today’s healthcare practice, oral antibiotics are used to reduce the production of propionate in people with PA/MMA. However oral antibiotics have several disadvantages, such as possible perturbation of normal gut microbiota, generating drug resistant bacteria and toxicity.
Need for a novel approach
Targeting the gut microbiota could be a new approach in the management of PA/MMA. This paper explores the potential role of gut microbiota in PA/MMA and proposes factors, known to modify the gut microbiota, to be considered for new comprehensive dietary management approaches.
Conclusions
New approaches are required to reduce the burden of propionate and therefore improve the clinical management of PA/MMA. This paper hypothesizes that the dietary management of PA/MMA may be improved by specific prebiotics that normalize gut microbiota while stabilizing or possibly reducing PA production. However, a more in-depth knowledge of gut microbiota composition and metabolic pathways in PA/MMA patients is a prerequisite for the development of successful dietary strategies.
View References
1 | Baumgartner MR, et al: Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. Orphanet J Rare Dis . Published on 2014;9:130 |
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2, 5 | Sutton VR, et al: Chronic management and health supervision of individuals with propionic acidemia. Mol Genet Metab. Published on 2012;105:26-33 |
3 | Aldubayan SH, Rodan LH, Berry GT, Levy HL: Acute illness protocol for organic acidemias: methylmalonic acidemia and propionic acidemia. Pediatr Emerg Care. Published on 2017;33:142-146 |
4 | Kolker S, et al: . The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. J Inherit Metab Dis. Published on 2015;38:1041-1057 |
6 | Fraser JL, Venditti CP, :Methylmalonic and propionic acidemias: clinical management update. Curr Opin Pediatr . Published on 2016;28:682-693 |
7 | Pena L, Burton BK, :Survey of health status and complications among propionic acidemia patients. Am J Med Genet A . Published on 2012;158A:1641-1646 |
8 | Kolker S, et al: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype. J Inherit Metab Dis. Published on 2015;38:1059-1074 |
9, 10 | Thompson GN, Walter JH, Bresson JL, Ford GC, Lyonnet SL, Chalmers RA, Saudubray JM, Leonard JV, Halliday D, (1990): Sources of propionate in inborn errors of propionate metabolism. Metabolism. Published on 39: 1133-1137 |
11 | Leonard JV, Stable isotope studies in propionic and methylmalonic acidaemia. Eur J Pediatr. Published on 1997;156 Suppl 1:S67-9 |