Literature DB >> 11196109

Plasma creatinine assessment in creatine deficiency: A diagnostic pitfall.

N M Verhoeven1, W S Guérand, E A Struys, A A Bouman, M S van der Knaap, C Jakobs.   

Abstract

Guanidinoacetate methyltransferase (GAMT) deficiency (creatine deficiency syndrome) is a recently discovered inborn error of creatine biosynthesis. Affected patients have elevated concentrations of guanidino-acetate, the metabolic precursor of creatine, in urine, plasma and cerebrospinal fluid. In addition, urinary creatinine excretion and plasma creatinine concentration are decreased. For biochemical evaluation of patients suspected to suffer from GAMT deficiency, correct quantification of creatinine in plasma is important. Here we report our experience with different quantification techniques. We found that creatinine in plasma from two GAMT-deficient patients appeared normal when measured by the Jaffé method but was decreased when measured enzymatically or by HPLC. The apparently normal levels of creatinine as measured by the Jaffé method were not caused by guanidinoacetate. In urine, the Jaffé method and the enzymatic method gave similar results, indicating that in urine no false elevations of creatinine can be expected. As the Jaffé method is still widely used for routine plasma creatinine measurements, it is important to realize it cannot be used to exclude GAMT deficiency.

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Year:  2000        PMID: 11196109     DOI: 10.1023/a:1026764703486

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  6 in total

1.  Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man.

Authors:  S Stöckler; D Isbrandt; F Hanefeld; B Schmidt; K von Figura
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

Review 2.  Analytical reviews in clinical biochemistry: the estimation of creatinine.

Authors:  K Spencer
Journal:  Ann Clin Biochem       Date:  1986-01       Impact factor: 2.057

3.  Guanidinoacetate methyltransferase deficiency: new clinical features.

Authors:  V Ganesan; A Johnson; A Connelly; S Eckhardt; R A Surtees
Journal:  Pediatr Neurol       Date:  1997-09       Impact factor: 3.372

4.  Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: diagnostic tools for a new inborn error of metabolism.

Authors:  A Schulze; T Hess; R Wevers; E Mayatepek; P Bachert; B Marescau; M V Knopp; P P De Deyn; H J Bremer; D Rating
Journal:  J Pediatr       Date:  1997-10       Impact factor: 4.406

5.  Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect.

Authors:  M S van der Knaap; N M Verhoeven; P Maaswinkel-Mooij; P J Pouwels; W Onkenhout; E A Peeters; S Stöckler-Ipsiroglu; C Jakobs
Journal:  Ann Neurol       Date:  2000-04       Impact factor: 10.422

6.  An accurate stable isotope dilution gas chromatographic-mass spectrometric approach to the diagnosis of guanidinoacetate methyltransferase deficiency.

Authors:  E A Struys; E E Jansen; H J ten Brink; N M Verhoeven; M S van der Knaap; C Jakobs
Journal:  J Pharm Biomed Anal       Date:  1998-12       Impact factor: 3.935

  6 in total
  5 in total

Review 1.  Proteomic studies on the development of the central nervous system and beyond.

Authors:  Chenggang Zhang
Journal:  Neurochem Res       Date:  2010-06-25       Impact factor: 3.996

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

Review 3.  Creatine deficiency syndromes.

Authors:  Andreas Schulze
Journal:  Mol Cell Biochem       Date:  2003-02       Impact factor: 3.396

4.  A Japanese adult case of guanidinoacetate methyltransferase deficiency.

Authors:  Tomoyuki Akiyama; Hitoshi Osaka; Hiroko Shimbo; Tomoshi Nakajiri; Katsuhiro Kobayashi; Makio Oka; Fumika Endoh; Harumi Yoshinaga
Journal:  JIMD Rep       Date:  2013-07-12

5.  Laboratory diagnosis of creatine deficiency syndromes: a technical standard and guideline of the American College of Medical Genetics and Genomics.

Authors:  J Daniel Sharer; Olaf Bodamer; Nicola Longo; Silvia Tortorelli; Mirjam M C Wamelink; Sarah Young
Journal:  Genet Med       Date:  2017-01-05       Impact factor: 8.822

  5 in total

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