Literature DB >> 1434508

Allopurinol challenge test in children.

A B Burlina1, V Ferrari, C Dionisi-Vici, A Bordugo, F Zacchello, M Tuchman.   

Abstract

The allopurinol challenge test was performed on 44 healthy subjects (28 children and 16 adolescents) in order to establish normal values of urinary orotic acid excretion following allopurinol ingestion in the paediatric population. The subjects were divided into three groups according to their age: 6 months to 6 years; 6 years to 10 years; and 10 years to 17 years. They were given 100 mg, 200 mg, or 300 mg of allopurinol, respectively (based on age) in a single oral dose. Maximum peak urinary orotic acid levels following ingestion of allopurinol were 13.0 (n = 14), 9.3 (n = 14), and 10.2 (n = 16) mumol/mmol creatinine in the three groups, respectively. In all children tested the peak orotic acid level was 3.1 +/- 2.7 mumol/mmol creatinine (mean +/- SD, n = 44). This allopurinol challenge test was also performed in six children with urea-cycle disorders, including five females with ornithine transcarbamylase (OTC) deficiency, all of whom demonstrated abnormally elevated levels of urinary orotic acid (peak levels of 26-134 mumol/mmol creatinine) following allopurinol ingestion.

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Year:  1992        PMID: 1434508     DOI: 10.1007/bf01800010

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


  12 in total

1.  Determination of urinary orotate excretion by high-performance liquid chromatography.

Authors:  V Ferrari; G Giordano; A T Cracco; N Dussini; L Chiandetti; F Zacchello
Journal:  J Chromatogr       Date:  1989-12-29

2.  Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women.

Authors:  E R Hauser; J E Finkelstein; D Valle; S W Brusilow
Journal:  N Engl J Med       Date:  1990-06-07       Impact factor: 91.245

3.  The orotic aciduria of pregnancy.

Authors:  M H Wood; W J O'Sullivan
Journal:  Am J Obstet Gynecol       Date:  1973-05-01       Impact factor: 8.661

4.  Episodic hyperammonemia in adult siblings with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.

Authors:  M Tuchman; D S Knopman; V E Shih
Journal:  Arch Neurol       Date:  1990-10

5.  Conditions affecting the colorimetry of orotic acid and orotidine in urine.

Authors:  M L Harris; V G Oberholzer
Journal:  Clin Chem       Date:  1980-03       Impact factor: 8.327

6.  Carrier detection in ornithine transcarbamylase deficiency.

Authors:  J T Hokanson; W E O'Brien; J Idemoto; I A Schafer
Journal:  J Pediatr       Date:  1978-07       Impact factor: 4.406

7.  Orotic aciduria in lysinuric protein intolerance: dependence on the urea cycle intermediates.

Authors:  J Rajantie
Journal:  Pediatr Res       Date:  1981-02       Impact factor: 3.756

8.  Orotidinuria induced by allopurinol.

Authors:  R M Fox; D Royse-Smith; W J O'Sullivan
Journal:  Science       Date:  1970-05-15       Impact factor: 47.728

9.  Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Authors:  O Simell; S Mackenzie; C L Clow; C R Scriver
Journal:  Pediatr Res       Date:  1985-12       Impact factor: 3.756

10.  Orotic aciduria in two unrelated patients with inherited deficiencies of purine nucleoside phosphorylase.

Authors:  A Cohen; G E Staal; A J Ammann; D W Martin
Journal:  J Clin Invest       Date:  1977-08       Impact factor: 14.808

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  12 in total

1.  Pitfalls in the detection of heterozygosity by allopurinol in a variant form of ornithine carbamoyltransferase deficiency.

Authors:  B A Barshop; W L Nyhan; C Climent; V Rubio
Journal:  J Inherit Metab Dis       Date:  2001-08       Impact factor: 4.982

2.  In vivo nitrogen metabolism in ornithine transcarbamylase deficiency.

Authors:  M Yudkoff; Y Daikhin; I Nissim; A Jawad; J Wilson; M Batshaw
Journal:  J Clin Invest       Date:  1996-11-01       Impact factor: 14.808

3.  Improved quality of life and unchanged magnetic resonance brain imaging after living donor liver transplantation for late-onset ornithine transcarbamylase deficiency: report of a case.

Authors:  Naoki Kawagishi; Kazushige Satoh; Yoshitaka Enomoto; Yorihiro Akamatsu; Satoshi Sekiguchi; Akira Satoh; Keisei Fujimori; Yuhei Takasago; Tetsuya Ito; Toshihiro Ohura; Susumu Satomi
Journal:  Surg Today       Date:  2005       Impact factor: 2.549

4.  The allopurinol loading test in detecting obligate heterozygotes for OCT deficiency.

Authors:  I Sebesta; J Krijt; L D Fairbanks; H A Simmonds
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

5.  The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease.

Authors:  J R Bonham; P Guthrie; M Downing; J C Allen; M S Tanner; M Sharrard; C Rittey; J M Land; A Fensom; D O'Neill; J A Duley; L D Fairbanks
Journal:  J Inherit Metab Dis       Date:  1999-04       Impact factor: 4.982

6.  Influence of dose and age on the response of the allopurinol test for ornithine carbamoyltransferase deficiency in control infants.

Authors:  E Riudor; J A Arranz; M Rodés; V Rubio; M Sentís; A B Burlina
Journal:  J Inherit Metab Dis       Date:  2000-11       Impact factor: 4.982

7.  In vivo urea cycle flux distinguishes and correlates with phenotypic severity in disorders of the urea cycle.

Authors:  B Lee; H Yu; F Jahoor; W O'Brien; A L Beaudet; P Reeds
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-05       Impact factor: 11.205

8.  In vivo measurement of ureagenesis with stable isotopes.

Authors:  M Yudkoff; Y Daikhin; X Ye; J M Wilson; M L Batshaw
Journal:  J Inherit Metab Dis       Date:  1998       Impact factor: 4.982

9.  Allopurinol challenge tests performed before and after living-related donor liver transplantation in citrullinaemia.

Authors:  T Ito; S Sumi; K Kidouchi; K Ban; A Ueta; T Hashimoto; H Togari; Y Wada
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

10.  How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?

Authors:  S Grünewald; L Fairbanks; S Genet; T Cranston; J Hüsing; J V Leonard; M P Champion
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

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