Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU)

M. Huemer, B. Simma, D. Mayr, D. Möslinger, A. Mühl, I. Schmid, H. Ulmer, O. A. Bodamer

Research output: Contribution to journalArticle

15 Scopus citations

Abstract

Introduction Free asymmetric dimethylarginine (ADMA) is a competitive inhibitor of the nitric oxide synthases (NOS). Suppression of nitric oxide (NO) synthesis increases the risk of atherosclerosis. Nevertheless, in the condition of oxidative stress, NOS blockade by ADMA may exert protective effects. Protein metabolism is altered in patients with phenylketonuria (PKU) on dietary treatment and as shown recently, oxidative stress is high in PKU. Since free ADMA concentrations are determined by both protein metabolism and oxidative stress we hypothesized, that free ADMA levels may be elevated in PKU patients. Design Sixteen patients with PKU on dietary treatment (mean age 10.1±5.2 yrs), and 91 healthy children (mean age 11.6± 3.7 yrs) participated in a cross sectional study. Results ADMA, total homocysteine (tHcy) and blood glucose were lower and the L-arginine/ADMA ratio was higher in PKU patients compared to controls. No significant correlation was present between phenylalanine (Phe) concentrations, protein intake, and lipid profile, history of cardiovascular disease or ADMA. Discussion In contrast to our hypothesis, ADMA was lower and the L-arginine/ADMA ratio was higher in PKU patients. Therefore, in PKU patients, the regulating function of ADMA on NO synthesis is altered and may thus contribute to oxidative stress.

Original languageEnglish (US)
Pages (from-to)817-821
Number of pages5
JournalJournal of Inherited Metabolic Disease
Volume35
Issue number5
DOIs
StatePublished - Sep 1 2012

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Huemer, M., Simma, B., Mayr, D., Möslinger, D., Mühl, A., Schmid, I., Ulmer, H., & Bodamer, O. A. (2012). Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU). Journal of Inherited Metabolic Disease, 35(5), 817-821. https://doi.org/10.1007/s10545-011-9448-8