Literature DB >> 17825809

Creatine transporter deficiency: prevalence among patients with mental retardation and pitfalls in metabolite screening.

Angela Arias1, Marc Corbella, Carmen Fons, Angela Sempere, Judit García-Villoria, Aida Ormazabal, Pilar Poo, Mercé Pineda, María Antonia Vilaseca, Jaume Campistol, Paz Briones, Teresa Pàmpols, Gajja S Salomons, Antonia Ribes, Rafael Artuch.   

Abstract

OBJECTIVES: To report the prevalence of creatine transporter deficiency in males with mental retardation and to study whether a protein-rich food intake might be a potential diagnostic pitfall. DESIGN AND METHODS: We determined creatine/creatinine ratio in urine samples from 1600 unrelated male patients with mental retardation and/or autism. Urine creatine was analyzed by HPLC-MS/MS.
RESULTS: Thirty-three of 1600 cases showed increased urine creatine/creatinine ratio. Four out of these thirty-three cases were definitively diagnosed with creatine transporter deficiency, while the other 29 were false positive results. Significantly higher values were observed for urine Cr/Crn ratio in healthy volunteers after a meal based on beef or oily fish as compared to eggs, pasta or salad (Wilcoxon test: p<0.005).
CONCLUSIONS: False positive results may be observed in biochemical screening for creatine transporter deficiency, and they may be due to intake of meals rich in creatine prior to urine samples analysis.

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Year:  2007        PMID: 17825809     DOI: 10.1016/j.clinbiochem.2007.07.010

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  21 in total

1.  Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome.

Authors:  Vassili Valayannopoulos; Naziha Bakouh; Michel Mazzuca; Luc Nonnenmacher; Laurence Hubert; Fatna-Léa Makaci; Allel Chabli; Gajja S Salomons; Caroline Mellot-Draznieks; Emilie Brulé; Pascale de Lonlay; Hervé Toulhoat; Arnold Munnich; Gabrielle Planelles; Yves de Keyzer
Journal:  J Inherit Metab Dis       Date:  2012-05-30       Impact factor: 4.982

2.  Effects of amide creatine derivatives in brain hippocampal slices, and their possible usefulness for curing creatine transporter deficiency.

Authors:  Patrizia Garbati; Enrico Adriano; Annalisa Salis; Silvia Ravera; Gianluca Damonte; Enrico Millo; Maurizio Balestrino
Journal:  Neurochem Res       Date:  2013-11-12       Impact factor: 3.996

3.  Altered carbon dioxide metabolism and creatine abnormalities in rett syndrome.

Authors:  Nicky S J Halbach; Eric E J Smeets; Jörgen Bierau; Irene M L W Keularts; Guy Plasqui; Peter O O Julu; Ingegerd Witt Engerström; Jaap A Bakker; Leopold M G Curfs
Journal:  JIMD Rep       Date:  2011-09-28

Review 4.  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

5.  Cyclocreatine treatment improves cognition in mice with creatine transporter deficiency.

Authors:  Yuko Kurosawa; Ton J Degrauw; Diana M Lindquist; Victor M Blanco; Gail J Pyne-Geithman; Takiko Daikoku; James B Chambers; Stephen C Benoit; Joseph F Clark
Journal:  J Clin Invest       Date:  2012-07-02       Impact factor: 14.808

Review 6.  Creatine as a Neuroprotector: an Actor that Can Play Many Parts.

Authors:  Eduardo Peil Marques; Angela T S Wyse
Journal:  Neurotox Res       Date:  2019-05-08       Impact factor: 3.911

7.  A Novel SLC6A8 Mutation in a Large Family with X-Linked Intellectual Disability: Clinical and Proton Magnetic Resonance Spectroscopy Data of Both Hemizygous Males and Heterozygous Females.

Authors:  S Dreha-Kulaczewski; V Kalscheuer; A Tzschach; H Hu; G Helms; K Brockmann; A Weddige; P Dechent; G Schlüter; R Krätzner; H-H Ropers; J Gärtner; B Zirn
Journal:  JIMD Rep       Date:  2013-11-05

8.  Creatine Transporter Deficiency: Screening of Males with Neurodevelopmental Disorders and Neurocognitive Characterization of a Case.

Authors:  Audrey Thurm; Daniel Himelstein; Precilla DʼSouza; Owen Rennert; Susanqi Jiang; Damilola Olatunji; Nicola Longo; Marzia Pasquali; Susan Swedo; Gajja S Salomons; Nuria Carrillo
Journal:  J Dev Behav Pediatr       Date:  2016-05       Impact factor: 2.225

Review 9.  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

10.  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

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