Literature DB >> 22644604

Creatine metabolism in urea cycle defects.

Sara Boenzi1, Anna Pastore, Diego Martinelli, Bianca Maria Goffredo, Arianna Boiani, Cristiano Rizzo, Carlo Dionisi-Vici.   

Abstract

Creatine (Cr) and phosphocreatine play an essential role in energy storage and transmission. Maintenance of creatine pool is provided by the diet and by de novo synthesis, which utilizes arginine, glycine and s-adenosylmethionine as substrates. Three primary Cr deficiencies exists: arginine:glycine amidinotransferase deficiency, guanidinoacetate methyltransferase deficiency and the defect of Cr transporter SLC6A8. Secondary Cr deficiency is characteristic of ornithine-aminotransferase deficiency, whereas non-uniform Cr abnormalities have anecdotally been reported in patients with urea cycle defects (UCDs), a disease category related to arginine metabolism in which Cr must be acquired by de novo synthesis because of low dietary intake. To evaluate the relationships between ureagenesis and Cr synthesis, we systematically measured plasma Cr in a large series of UCD patients (i.e., OTC, ASS, ASL deficiencies, HHH syndrome and lysinuric protein intolerance). Plasma Cr concentrations in UCDs followed two different trends: patients with OTC and ASS deficiencies and HHH syndrome presented a significant Cr decrease, whereas in ASL deficiency and lysinuric protein intolerance Cr levels were significantly increased (23.5 vs. 82.6 μmol/L; p < 0.0001). This trend distribution appears to be regulated upon cellular arginine availability, highlighting its crucial role for both ureagenesis and Cr synthesis. Although decreased Cr contributes to the neurological symptoms in primary Cr deficiencies, still remains to be explored if an altered Cr metabolism may participate to CNS dysfunction also in patients with UCDs. Since arginine in most UCDs becomes a semi-essential aminoacid, measuring plasma Cr concentrations might be of help to optimize the dose of arginine substitution.

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Year:  2012        PMID: 22644604     DOI: 10.1007/s10545-012-9494-x

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


  45 in total

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Authors:  Hélène Ogier de Baulny; Manuel Schiff; Carlo Dionisi-Vici
Journal:  Mol Genet Metab       Date:  2012-02-17       Impact factor: 4.797

2.  Guanidino compound levels in blood, cerebrospinal fluid, and post-mortem brain material of patients with argininemia.

Authors:  Joshua L Deignan; Peter P De Deyn; Stephen D Cederbaum; Arno Fuchshuber; Bernhard Roth; Wieland Gsell; Bart Marescau
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Review 3.  Synthesis and transport of creatine in the CNS: importance for cerebral functions.

Authors:  Elidie Béard; Olivier Braissant
Journal:  J Neurochem       Date:  2010-08-25       Impact factor: 5.372

4.  Usefulness of magnetic resonance spectroscopy in urea cycle disorders.

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Journal:  Pediatr Neurol       Date:  2007-09       Impact factor: 3.372

5.  1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

Authors:  A L Gropman; S T Fricke; R R Seltzer; A Hailu; A Adeyemo; A Sawyer; J van Meter; W D Gaillard; R McCarter; M Tuchman; M Batshaw
Journal:  Mol Genet Metab       Date:  2008-07-26       Impact factor: 4.797

6.  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

7.  Lysinuric protein intolerance mutation is expressed in the plasma membrane of cultured skin fibroblasts.

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8.  Guanidinoacetate and creatine/creatinine levels in controls and patients with urea cycle defects.

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Journal:  Mol Genet Metab       Date:  2004-07       Impact factor: 4.797

9.  Secondary creatine deficiency in ornithine delta-aminotransferase deficiency.

Authors:  V Valayannopoulos; N Boddaert; K Mention; G Touati; V Barbier; A Chabli; F Sedel; J Kaplan; J L Dufier; David Seidenwurm; D Rabier; J M Saudubray; P de Lonlay
Journal:  Mol Genet Metab       Date:  2009-03-31       Impact factor: 4.797

Review 10.  Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyond.

Authors:  Ayelet Erez; Sandesh C Sreenath Nagamani; Brendan Lee
Journal:  Am J Med Genet C Semin Med Genet       Date:  2011-02-10       Impact factor: 3.908

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Journal:  Genet Med       Date:  2017-01-05       Impact factor: 8.822

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3.  Expanding the phenotype in argininosuccinic aciduria: need for new therapies.

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Journal:  J Inherit Metab Dis       Date:  2017-03-01       Impact factor: 4.982

Review 4.  Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle Metabolism.

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Journal:  Front Neurol       Date:  2019-02-22       Impact factor: 4.003

Review 5.  Protein Aggregation Inhibitors as Disease-Modifying Therapies for Polyglutamine Diseases.

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6.  Usefulness of serum BUN or BUN/creatinine ratio as markers for citrin deficiency in positive cases of newborn screening.

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Journal:  Mol Genet Metab Rep       Date:  2021-12-20

7.  Urea Cycle Related Amino Acids Measured in Dried Bloodspots Enable Long-Term In Vivo Monitoring and Therapeutic Adjustment.

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