1-13C-propionate breath testing as a surrogate endpoint to assess efficacy of liver-directed therapies in methylmalonic acidemia (MMA)

Purpose

To develop a safe and noninvasive in vivo assay of hepatic propionate oxidative capacity.

Methods

A modified 1-¹³C-propionate breath test was administered to 57 methylmalonic acidemia (MMA) subjects, including 19 transplant recipients, and 16 healthy volunteers. Isotopomer enrichment (¹³CO₂/¹²CO₂) was measured in exhaled breath after an enteral bolus of sodium-1-¹³C-propionate, and normalized for CO₂ production. 1-¹³C-propionate oxidation was then correlated with clinical, laboratory, and imaging parameters collected via a dedicated natural history protocol.

Results

Lower propionate oxidation was observed in patients with the severe mut⁰ and cblB subtypes of MMA, but was near normal in those with the cblA and mut⁻ forms of the disorder. Liver transplant recipients demonstrated complete restoration of 1-¹³C-propionate oxidation to control levels. 1-¹³C-propionate oxidation correlated with cognitive test result, growth indices, bone mineral density, renal function, and serum biomarkers. Test repeatability was robust in controls and in MMA subjects (mean coefficient of variation 6.9% and 12.8%, respectively), despite widely variable serum methylmalonic acid concentrations in the patients.

Conclusion

Propionate oxidative capacity, as measured with 1-¹³C-propionate breath testing, predicts disease severity and clinical outcomes, and could be used to assess the therapeutic effects of liver-targeted genomic therapies for MMA and related disorders of propionate metabolism.