AI Article Synopsis

  • An adult female patient with arginase 1 deficiency (ARG1-D) was diagnosed as a child and managed with a combination of protein restriction and sodium benzoate therapy, which initially controlled hyperammonemia but not hyperargininemia.
  • After experiencing severe drops in serum albumin levels, her condition worsened until sodium phenylbutyrate (NaPB) therapy was introduced, leading to significant clinical and metabolic improvement.
  • Current treatments for ARG1-D focus on reducing plasma arginine levels, utilizing nitrogen scavengers like NaPB to bypass the urea cycle and remove nitrogen, which helps prevent complications from low protein intake.

Article Abstract

An adult female patient was diagnosed with arginase 1 deficiency (ARG1-D) at 4 years of age, and had been managed with protein restriction combined with sodium benzoate therapy. Though the treatment was successful in ameliorating hyperammonemia, hyperargininemia persisted. After being under control with a strict restriction of dietary protein, severe fall of serum albumin levels appeared and her condition became strikingly worsened. However, after sodium phenylbutyrate (NaPB) therapy was initiated, the clinical condition and metabolic stability was greatly improved. Current management of ARG1-D is aimed at lowering plasma arginine levels. The nitrogen scavengers, such as NaPB can excrete the waste nitrogen not through the urea cycle but via the alternative pathway. The removal of nitrogen via alternative pathway lowers the flux of arginine in the urea cycle. Thereby, the clinical complications due to insufficient amount of protein intake can be prevented. Thus, NaPB therapy can be expected as a useful therapeutic option, particularly in patients with ARG1-D.

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Source
http://dx.doi.org/10.1016/j.braindev.2019.09.002DOI Listing

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