Literature DB >> 3409923

Low biotinidase activity in plasma of some preterm infants: possible source of false-positive screening results.

T Suormala1, H Wick, E R Baumgartner.   

Abstract

Screening for biotinidase deficiency has been added recently to some national screening programmes. To clarify the problem of false-positive screening tests in premature infants, we have studied biotinidase activities in the plasma of this population in more detail. In 64 newborns (premature and term babies) biotinidase activities correlated positively with gestational age from the 2nd to the 30th day of life. During the 1st-3rd day the activities were below the normal adult range in all 64 infants. In 56 infants the activities subsequently increased gradually and reached the normal adult range during the 4th-40th day of life. In contrast, the biotinidase activities in eight preterm infants dropped during the 3rd-7th day of life. Impaired liver function as a possible cause for this finding could be ruled out in these infants. The lowest activities in these infants were measured during the 4th-6th day of life, i.e. unfortunately at a time when samples for the screening are normally taken. According to our data, 4-8 out of 48 preterm or small-for-date infants with biotinidase activities ranging from 4.7%-26% of the mean adult value would have given false-positive screening tests. A positive screening test was also obtained in a newborn and in an older unrelated child with a partial biotinidase deficiency. In these children the biotinidase activity did not rise but remained slightly below or at the lower range for heterozygotes (at 31% and 38% of the mean adult value). Currently we do not know whether such individuals are heterozygotes, or whether they have a variant of biotinidase deficiency. However, these children have developed normally without biotin therapy.

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Year:  1988        PMID: 3409923     DOI: 10.1007/bf00441970

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  9 in total

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Authors:  J Oizumi; K Hayakawa; K Iinuma; Y Odajima; Y Iikura
Journal:  J Pediatr       Date:  1987-05       Impact factor: 4.406

4.  Changes in the physicochemical characteristics of rabbit liver N-acetyltransferase during post-natal development.

Authors:  S N Cohen; R Baumgartner; M S Steinberg; W W Weber
Journal:  Biochim Biophys Acta       Date:  1973-04-28

5.  Neonatal screening for biotinidase deficiency: results of a 1-year pilot study.

Authors:  G S Heard; B Wolf; L G Jefferson; K A Weissbecker; W E Nance; J R McVoy; A Napolitano; P L Mitchell; F W Lambert; A S Linyear
Journal:  J Pediatr       Date:  1986-01       Impact factor: 4.406

6.  Deficient biotinidase activity in late-onset multiple carboxylase deficiency.

Authors:  B Wolf; R E Grier; W D Parker; S I Goodman; R J Allen
Journal:  N Engl J Med       Date:  1983-01-20       Impact factor: 91.245

7.  [Results of a pilot study of neonatal screening for congenital biotinidase deficiency].

Authors:  J Sander; C Niehaus
Journal:  Monatsschr Kinderheilkd       Date:  1986-10       Impact factor: 0.323

8.  A screening method for biotinidase deficiency in newborns.

Authors:  G S Heard; J R Secor McVoy; B Wolf
Journal:  Clin Chem       Date:  1984-01       Impact factor: 8.327

9.  Biotinidase deficiency associated with renal loss of biocytin and biotin.

Authors:  E R Baumgartner; T Suormala; H Wick; J Bausch; J P Bonjour
Journal:  Ann N Y Acad Sci       Date:  1985       Impact factor: 5.691

  9 in total
  7 in total

1.  Comparison of patients with complete and partial biotinidase deficiency: biochemical studies.

Authors:  T M Suormala; E R Baumgartner; H Wick; S Scheibenreiter; S Schweitzer
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Neonatal screening for profound biotinidase deficiency in the Netherlands: consequences and considerations.

Authors:  Rachel C Wiltink; Michelle E Kruijshaar; Rick van Minkelen; Willem Onkenhout; Frans W Verheijen; Evelien A Kemper; Francjan J van Spronsen; Ans T van der Ploeg; Klary E Niezen-Koning; Jasper J Saris; Monique Williams
Journal:  Eur J Hum Genet       Date:  2016-06-22       Impact factor: 4.246

3.  Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics.

Authors:  Erin T Strovel; Tina M Cowan; Anna I Scott; Barry Wolf
Journal:  Genet Med       Date:  2017-07-05       Impact factor: 8.822

4.  Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients.

Authors:  Taciane Borsatto; Fernanda Sperb-Ludwig; Samyra E Lima; Maria R S Carvalho; Pablo A S Fonseca; José S Camelo; Erlane M Ribeiro; Paula F V de Medeiros; Charles M Lourenço; Carolina F M de Souza; Raquel Boy; Têmis M Félix; Camila M Bittar; Louise L C Pinto; Eurico C Neto; Henk J Blom; Ida V D Schwartz
Journal:  PLoS One       Date:  2017-05-12       Impact factor: 3.240

Review 5.  Biotinidase Deficiency: Prevalence, Impact And Management Strategies.

Authors:  Ebru Canda; Sema Kalkan Uçar; Mahmut Çoker
Journal:  Pediatric Health Med Ther       Date:  2020-05-04

6.  Application of a next-generation sequencing (NGS) panel in newborn screening efficiently identifies inborn disorders of neonates.

Authors:  Xinwen Huang; Dingwen Wu; Lin Zhu; Wenjun Wang; Rulai Yang; Jianbin Yang; Qunyan He; Bingquan Zhu; Ying You; Rui Xiao; Zhengyan Zhao
Journal:  Orphanet J Rare Dis       Date:  2022-02-21       Impact factor: 4.123

7.  Biotinidase deficiency: clinical and genetic studies of 38 Brazilian patients.

Authors:  Taciane Borsatto; Fernanda Sperb-Ludwig; Louise L C Pinto; Gisele R De Luca; Francisca L Carvalho; Carolina F M De Souza; Paula F V De Medeiros; Charles M Lourenço; Reinaldo Lo Filho; Eurico C Neto; Pricila Bernardi; Sandra Leistner-Segal; Ida V Schwartz
Journal:  BMC Med Genet       Date:  2014-09-01       Impact factor: 2.103

  7 in total

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