Literature DB >> 11412830

Analysis of guanidinoacetate and creatine by isotope dilution electrospray tandem mass spectrometry.

O A Bodamer1, S M Bloesch, A R Gregg, S Stockler-Ipsiroglu, W E O'Brien.   

Abstract

Guanidinoacetate methyltransferase (GAMT) deficiency is a disorder of creatine metabolism characterized by low plasma creatine concentrations in combination with elevated guanidinoacetate (GAA) concentrations. Although rare, GAMT deficiency has been identified in children with seizures, extrapyramidal movements, developmental delay, myopathies and behavioral abnormalities. Treatment with creatine monohydrate has been proven to be effective. We describe an isotope dilution electrospray tandem mass spectrometry (ES-MS/MS) assay for the simultaneous determination of plasma GAA and creatine using multiple reaction monitoring (MRM), d(3)-creatine as the internal standard and derivatization of GAA and creatine as butyl-esters. We analysed plasma of 16 healthy adults and 20 healthy children as well as three affected children. Plasma GAA concentrations were 5.02+/-1.84 micromol/l (mean+/-S.D.) in adults, 3.91+/-0.76 micromol/l in children age 5-10 years and 11.57, 15.16, 14.36 micromol/l in children with GAMT deficiency. Plasma creatine concentrations were 34.7+/-15.25 micromol/l in adults, 58.96+/-22.30 micromol/l in children and 5.37, 8.15, 403.5 micromol/l in two untreated children and one treated child with GAMT deficiency, respectively. GAA can also be reliably measured from filter cards, which is sufficient to make the correct diagnosis while creatine is consistently falsely elevated probably secondary to liberation of red cell creatine. In nine healthy newborn infants, GAA concentrations from filter cards were 4.83+/-1.43 and 5.04+/-1.84 micromol/l in 16 healthy adults. We conclude that isotope dilution ES-MS/MS is ideal for rapid high-throughput diagnosis of GAMT deficiency both from plasma and filter paper cards. Using this technique neonatal screening is feasible for this treatable inborn error of creatine metabolism.

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Year:  2001        PMID: 11412830     DOI: 10.1016/s0009-8981(01)00480-6

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  15 in total

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2.  Biochemical and behavioral phenotype of AGAT and GAMT deficient mice following long-term Creatine monohydrate supplementation.

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Journal:  Metab Brain Dis       Date:  2017-08-14       Impact factor: 3.584

3.  Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humans.

Authors:  C B Item; S Stöckler-Ipsiroglu; C Stromberger; A Mühl; M G Alessandrì; M C Bianchi; M Tosetti; F Fornai; G Cioni
Journal:  Am J Hum Genet       Date:  2001-09-10       Impact factor: 11.025

4.  Mutation in the Monocarboxylate Transporter 12 Gene Affects Guanidinoacetate Excretion but Does Not Cause Glucosuria.

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Journal:  J Am Soc Nephrol       Date:  2015-09-16       Impact factor: 10.121

Review 5.  X-linked creatine transporter deficiency: clinical aspects and pathophysiology.

Authors:  Jiddeke M van de Kamp; Grazia M Mancini; Gajja S Salomons
Journal:  J Inherit Metab Dis       Date:  2014-05-01       Impact factor: 4.982

6.  Homocystinuria due to cystathionine beta-synthase deficiency: novel biochemical findings and treatment efficacy.

Authors:  M Orendác; J Zeman; S P Stabler; R H Allen; J P Kraus; O Bodamer; S Stöckler-Ipsiroglu; J Kvasnicka; V Kozich
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 7.  Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism.

Authors:  C Stromberger; O A Bodamer; S Stöckler-Ipsiroglu
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

8.  The effect of L-arginine and creatine on vascular function and homocysteine metabolism.

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9.  Simultaneous assay of isotopic enrichment and concentration of guanidinoacetate and creatine by gas chromatography-mass spectrometry.

Authors:  Takhar Kasumov; Lourdes L Gruca; Srinivasan Dasarathy; Satish C Kalhan
Journal:  Anal Biochem       Date:  2009-07-29       Impact factor: 3.365

10.  GAMT, a p53-inducible modulator of apoptosis, is critical for the adaptive response to nutrient stress.

Authors:  Takao Ide; Lauren Brown-Endres; Kiki Chu; Pat P Ongusaha; Takao Ohtsuka; Wafik S El-Deiry; Stuart A Aaronson; Sam W Lee
Journal:  Mol Cell       Date:  2009-11-13       Impact factor: 17.970

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