Literature DB >> 16621013

Methods for the diagnosis of creatine deficiency syndromes: a comparative study.

Angela Arias1, Aida Ormazabal, Juan Moreno, Bernardino González, Maria Antonia Vilaseca, Judit García-Villoria, Teresa Pàmpols, Paz Briones, Rafael Artuch, Antonia Ribes.   

Abstract

The increasing number of patients with creatine deficiency syndromes (CDS) stresses the need to develop screening procedures for the identification these inherited disorders. Guanidinoacetate (GAA) and creatine (Cr) are reliable biochemical markers of CDS and several analytical methods to measure both metabolites have been developed. High-pressure liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) is quick and sensitive but, unlike HPLC and gas chromatography-mass spectrometry (GC/MS), it is unavailable in most laboratories. Thus, we decided to evaluate comparatively HPLC-MS/MS, GC/MS and HPLC methods, as well as to establish reference values in a healthy paediatric population. According to our results, these three methods may be suitable for analysing GAA in urine. Furthermore, Passing-Bablock plots showed good agreement among all three. However, when comparing the Cr/Crn ratio, our results revealed that while HPLC-MS/MS data were in agreement with those of GC/MS, a constant and proportional error was observed when compared with those of HPLC. Consequently, the Cr/Crn ratio obtained by the last method should be evaluated with caution. Our reference values for GAA and Cr/Crn ratio in urine negatively correlate with age. Concerning GAA and Cr measurements in plasma, it is interesting to note that in contrast to what was occurring in urine, GAA concentration increased significantly with age, while we did not find any significant difference for Cr values within the same age group.

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Year:  2006        PMID: 16621013     DOI: 10.1016/j.jneumeth.2006.03.005

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  8 in total

1.  Glycine and L-arginine treatment causes hyperhomocysteinemia in cerebral creatine transporter deficiency patients.

Authors:  Cristina Villar; Jaume Campistol; Carmen Fons; Judith Armstrong; Anna Mas; Aida Ormazabal; Rafael Artuch
Journal:  JIMD Rep       Date:  2011-11-04

Review 2.  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

3.  Cooperative Binding of Substrate and Ions Drives Forward Cycling of the Human Creatine Transporter-1.

Authors:  Clemens V Farr; Ali El-Kasaby; Fatma A Erdem; Sonja Sucic; Michael Freissmuth; Walter Sandtner
Journal:  Front Physiol       Date:  2022-06-28       Impact factor: 4.755

4.  Arginine supplementation in four patients with X-linked creatine transporter defect.

Authors:  C Fons; A Sempere; A Arias; A López-Sala; P Póo; M Pineda; A Mas; M A Vilaseca; G S Salomons; A Ribes; R Artuch; J Campistol
Journal:  J Inherit Metab Dis       Date:  2008-10-16       Impact factor: 4.982

5.  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

Review 6.  Creatine transporter deficiency in two adult patients with static encephalopathy.

Authors:  A Sempere; C Fons; A Arias; P Rodríguez-Pombo; R Colomer; B Merinero; P Alcaide; A Capdevila; A Ribes; R Artuch; J Campistol
Journal:  J Inherit Metab Dis       Date:  2009-03-25       Impact factor: 4.982

7.  Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency.

Authors:  Martina Huemer; Daniel R Carvalho; Jaime M Brum; Özlem Ünal; Turgay Coskun; James D Weisfeld-Adams; Nina L Schrager; Sabine Scholl-Bürgi; Andrea Schlune; Markus G Donner; Martin Hersberger; Claudio Gemperle; Brunhilde Riesner; Hanno Ulmer; Johannes Häberle; Daniela Karall
Journal:  J Inherit Metab Dis       Date:  2016-04-01       Impact factor: 4.982

8.  Study of inborn errors of metabolism in urine from patients with unexplained mental retardation.

Authors:  Angela Sempere; Angela Arias; Guillermo Farré; Judith García-Villoria; Pilar Rodríguez-Pombo; Lurdes R Desviat; Begoña Merinero; Angels García-Cazorla; Maria A Vilaseca; Antonia Ribes; Rafael Artuch; Jaume Campistol
Journal:  J Inherit Metab Dis       Date:  2010-01-05       Impact factor: 4.982

  8 in total

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