Biomarkers to predict disease progression and therapeutic response in isolated methylmalonic acidemia (MMA).
Irini ManoliAbigael GebremariamSamantha McCoyAlexandra R PassJack GagnéCamryn HallSusan FerryCarol Van RyzinJennifer L SloanElisa SacchettiGiulio CatesiniCristiano RizzoDiego MartinelliMarco SpadaCarlo Dionisi-ViciCharles P VendittiPublished in: Journal of inherited metabolic disease (2023)
Methylmalonic Acidemia (MMA) is a heterogenous group of inborn errors of metabolism caused by a defect in the methylmalonyl-CoA mutase (MMUT) enzyme or the synthesis and transport of its cofactor, 5'-deoxy- adenosylcobalamin. It is characterized by life-threatening episodes of ketoacidosis, chronic kidney disease, and other multiorgan complications. Liver transplantation can improve patient stability and survival and thus provides clinical and biochemical benchmarks for the development of hepatocyte-targeted genomic therapies. Data are presented from a US natural history protocol that evaluated subjects with different types of MMA including mut- (N=91), cblB- (15), and cblA-type MMA (17), as well as from an Italian cohort of mut- (N=19) and cblB-type MMA (N=2) subjects, including data before and after organ transplantation in both cohorts. Canonical metabolic markers, such as serum methylmalonic acid and propionylcarnitine, are variable and affected by dietary intake and renal function. We have therefore explored the use of the 1- 13 C-propionate oxidation breath test (POBT) to measure metabolic capacity and the changes in circulating proteins to assess mitochondrial dysfunction (fibroblast growth factor-21, FGF-21 and growth differentiation factor-15, GDF-15) and kidney injury (lipocalin-2, LCN2). Biomarker concentrations are higher in patients with the severe mut 0 - and cblB-type MMA, correlate with a decreased POBT, and show a significant response post-liver transplant. Additional circulating and imaging markers to assess disease burden are necessary to monitor disease progression. A combination of biomarkers reflecting disease severity and multisystem involvement will be needed to help stratify patients for clinical trials and assess the efficacy of new therapies for MMA. This article is protected by copyright. All rights reserved.