Literature DB >> 15159648

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

S Grünewald1, L Fairbanks, S Genet, T Cranston, J Hüsing, J V Leonard, M P Champion.   

Abstract

The allopurinol test aims to distinguish carriers and noncarriers for ornithine transcarbamylase (OTC) deficiency. We have evaluated the reliability of the test in at-risk females of known genotype. Results based on urine orotidine and/or orotic acid measurement were compared in terms of sensitivity and specificity. Retrospectively, we analysed the results of allopurinol tests in 42 women (22 confirmed heterozygotes and 20 noncarriers) from 23 pedigrees at risk of being carriers for OTC deficiency. Using a cut-off of 2 standard deviations above the mean of controls, the highest sensitivity (91%) was given by orotidine alone or in combination with orotic acid, but specificity was only 70% and 65%, respectively. We conclude that the value of the allopurinol test for detecting OTC carriers in at-risk females is limited. This needs to be recognized when counselling families. The test still has a role as a safe, quick, noninvasive screen of individuals at risk, but test results in possible carriers should be interpreted with caution. In the absence of other supportive evidence, confirmation by mutation analysis is required.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15159648     DOI: 10.1023/B:BOLI.0000028727.77454.bd

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


  32 in total

1.  Neurological outcome of patients with ornithine carbamoyltransferase deficiency.

Authors:  P Nicolaides; D Liebsch; N Dale; J Leonard; R Surtees
Journal:  Arch Dis Child       Date:  2002-01       Impact factor: 3.791

2.  Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.

Authors:  P H Arn; E R Hauser; G H Thomas; G Herman; D Hess; S W Brusilow
Journal:  N Engl J Med       Date:  1990-06-07       Impact factor: 91.245

3.  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

4.  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

5.  Optimization of allopurinol challenge: sample purification, protein intake control, and the use of orotidine response as a discriminative variable improve performance of the test for diagnosing ornithine carbamoyltransferase deficiency.

Authors:  J A Arranz; E Riudor; M Rodés; M Roig; C Climent; V Rubio; M Sentís; A Burlina
Journal:  Clin Chem       Date:  1999-07       Impact factor: 8.327

6.  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

7.  Maternal gonadal mosaicism causing ornithine transcarbamylase deficiency.

Authors:  F Bowling; I McGown; J McGill; D Cowley; M Tuchman
Journal:  Am J Med Genet       Date:  1999-08-27

8.  Ornithine carbamoyltransferase deficiency: improved sensitivity of testing for protein tolerance in the diagnosis of heterozygotes.

Authors:  M Potter; J W Hammond; K G Sim; A K Green; B Wilcken
Journal:  J Inherit Metab Dis       Date:  2001-02       Impact factor: 4.982

9.  Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.

Authors:  M L Batshaw; M Msall; A L Beaudet; J Trojak
Journal:  J Pediatr       Date:  1986-02       Impact factor: 4.406

10.  The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.

Authors:  N E Maestri; C Lord; M Glynn; A Bale; S W Brusilow
Journal:  Medicine (Baltimore)       Date:  1998-11       Impact factor: 1.889

View more
  5 in total

1.  Calculation of the reliability of the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency.

Authors:  Konrad Oexle
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

2.  Biochemical data in ornithine transcarbamylase deficiency (OTCD) carrier risk estimation: logistic discrimination and combination with genetic information.

Authors:  Konrad Oexle
Journal:  J Hum Genet       Date:  2006-02-02       Impact factor: 3.172

Review 3.  Orotic aciduria and uridine monophosphate synthase: a reappraisal.

Authors:  C J Bailey
Journal:  J Inherit Metab Dis       Date:  2009-06-27       Impact factor: 4.982

4.  Humanized liver mouse model with transplanted human hepatocytes from patients with ornithine transcarbamylase deficiency.

Authors:  Go Sugahara; Chihiro Yamasaki; Ami Yanagi; Suzue Furukawa; Yuko Ogawa; Akinari Fukuda; Shin Enosawa; Akihiro Umezawa; Yuji Ishida; Chise Tateno
Journal:  J Inherit Metab Dis       Date:  2020-12-30       Impact factor: 4.982

Review 5.  Suggested guidelines for the diagnosis and management of urea cycle disorders.

Authors:  Johannes Häberle; Nathalie Boddaert; Alberto Burlina; Anupam Chakrapani; Marjorie Dixon; Martina Huemer; Daniela Karall; Diego Martinelli; Pablo Sanjurjo Crespo; René Santer; Aude Servais; Vassili Valayannopoulos; Martin Lindner; Vicente Rubio; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2012-05-29       Impact factor: 4.123

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.