Guanidino Compound Analysis as a Complementary Diagnostic Parameter for Hyperargininemia: Follow-Up of Guanidino Compound Levels during Therapy
- 1 March 1990
- journal article
- research article
- Published by Springer Nature in Pediatric Research
- Vol. 27 (3), 297-303
- https://doi.org/10.1203/00006450-199003000-00020
Abstract
The aim of this collaborative study was to investigate whether guanidino compound analyses in the biologic fluids can be used as a complementary diagnostic parameter for hyperargininemia. Guanidino compounds were determined in the biologic fluids of all known living hyperargininemic patients using a cation exchange Chromatographie system with a fluorescence detection method. The serum arginine, homoarginine, α-keto-δ-guanidino-valeric acid, argininic acid, and N-α-acetylarginine levels of all the hyperargininemic patients are higher than the normal range. Similar increases were seen for the urinary excretion of α-keto-δ-guanidinovaleric acid and argininic acid. Untreated hyperargininemic patients have the highest guanidino compound levels in cerebrospinal fluid. However, even under therapy, the arginine, homoarginine, α-keto-δ-guanidinovaleric acid, and argininic acid levels in cerebrospinal fluid are still increased. Protein restriction alone is not sufficient to normalize the hyperargininemia, but protein restriction together with supplementation of essential amino acids with or without sodium benzoate decreases further the arginine levels. However, whereas the argininemia can be normalized, the catabolites of arginine are still increased. We conclude that the urinary amino acid levels may remain normal in hyperargininemia, whereas consistent increases of the guanidino compounds are observed. Thus, guanidino compound analyses can be used as a complementary biochemical diagnostic parameter for hyperargininemia. Although the argininemia can be normalized by therapy, the levels of the catabolites of arginine are still elevated.Keywords
This publication has 10 references indexed in Scilit:
- A new case of arginase deficiency in a Spanish maleJournal of Inherited Metabolic Disease, 1986
- Guanidino compounds in plasma, urine and cerebrospinal fluid of hyperargininemic patients during therapyClinica Chimica Acta; International Journal of Clinical Chemistry, 1985
- Treatment of hyperargininemia with sodium benzoate and arginine-restricted dietThe Journal of Pediatrics, 1984
- A new French‐Canadian family affected by hyperargininaemiaJournal of Inherited Metabolic Disease, 1983
- Argininemia treated from birthThe Journal of Pediatrics, 1979
- Hyperargininemia with Arginase DeficiencyPediatric Research, 1979
- Arginase deficiency in multiple tissues in argininemiaClinical Genetics, 1978
- HyperargininemiaThe Journal of Pediatrics, 1977
- ArgininemiaThe Journal of Pediatrics, 1977
- Homocitrulline and Homoarginine Synthesis from LysineScience, 1964