Literature DB >> 30136145

Neonatal screening in the Czech Republic: increased prevalence of selected diseases in low birthweight neonates.

Jan David1, Petr Chrastina2, Hana Vinohradska3, Eva Al Taji4, Andrea Holubova5, Eva Hlidkova6, Viktor Kozich2, Felix Votava4.   

Abstract

Neonates with low birthweight (LBW) represent a vulnerable population. This retrospective study analyzed the birth frequency of diseases detected by neonatal screening (NBS) in normal and LBW neonates in the Czech Republic. Between years 2002 and 2016, the number of screened disorders in the Czech Republic gradually increased from two to 13. Prevalence of screened diseases was calculated for cohorts ranging from 777,100 to 1,277,283 neonates stratified by birthweight. Odds ratio of the association of LBW with each disease was calculated and statistical significance was evaluated using the chi-square test or Fisher's exact test, as appropriate. Three diseases were associated with higher risk of prevalence in LBW neonates, namely congenital hypothyroidism (OR 2.50, CI 1.92; 3.25), cystic fibrosis (OR 2.44, CI 1.51; 3.94), and long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) (OR 7.74, CI 2.18; 27.42).
Conclusion: Although the underlying mechanisms are not well understood, results can be hypothesized that LBW (respectively prematurity) may lead to the secondary and often transitory hypothyroidism while cystic fibrosis and LCHADD may manifest already prenatally and result into preterm birth and LBW. What is Known: • The percentage of low birthweight (LBW) neonates in the Czech Republic has been increasing. • Previously published studies reported positive association between LBW and congenital hypothyroidism and cystic fibrosis. What is New: • The association between LCHADD and LBW has not yet been described. • LBW can be the first manifestation of cystic fibrosis and LCHADD.

Entities:  

Keywords:  Congenital hypothyroidism; Cystic fibrosis; Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency; Low birthweight; Neonatal screening

Mesh:

Year:  2018        PMID: 30136145     DOI: 10.1007/s00431-018-3230-y

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


  27 in total

1.  Screening for congenital hypothyroidism: the value of retesting after four weeks in neonates with low and very low birth weight.

Authors:  Dorota Tylek-Lemańska; Małgorzata Kumorowicz-Kopiec; Jerzy Starzyk
Journal:  J Med Screen       Date:  2005       Impact factor: 2.136

Review 2.  Newborn screening for congenital hypothyroidism.

Authors:  Atilla Büyükgebiz
Journal:  J Pediatr Endocrinol Metab       Date:  2006-11       Impact factor: 1.634

3.  Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations.

Authors:  Olaf Sommerburg; Veronika Krulisova; Jutta Hammermann; Martin Lindner; Mirjam Stahl; Martina Muckenthaler; Dirk Kohlmueller; Margit Happich; Andreas E Kulozik; Felix Votava; Miroslava Balascakova; Veronika Skalicka; Marina Stopsack; Manfred Gahr; Milan Macek; Marcus A Mall; Georg F Hoffmann
Journal:  J Cyst Fibros       Date:  2013-07-25       Impact factor: 5.482

Review 4.  Newborn screening for medium chain acyl CoA dehydrogenase deficiency.

Authors:  J V Leonard; C Dezateux
Journal:  Arch Dis Child       Date:  2008-10-06       Impact factor: 3.791

5.  [Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, association with HELLP and magnetic resonance spectroscopy findings].

Authors:  Noelia Deltetto; Clarisa Maxit; Delfina Marchione; Marina Szlago; Andrea Schenone; Cristina H Besada; María Vaccarezza; Guillermo Agosta
Journal:  Arch Argent Pediatr       Date:  2012-08       Impact factor: 0.635

6.  Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance.

Authors:  Felix Votava; Dana Novotna; Petr Kracmar; Hana Vinohradska; Eva Stahlova-Hrabincova; Zuzana Vrzalova; David Neumann; Jana Malikova; Jan Lebl; Dietrich Matern
Journal:  Eur J Pediatr       Date:  2012-01-11       Impact factor: 3.183

Review 7.  Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation.

Authors:  Bijay Vaidya; Viv Campbell; John H Tripp; Gill Spyer; Andrew T Hattersley; Sian Ellard
Journal:  Clin Endocrinol (Oxf)       Date:  2004-06       Impact factor: 3.478

8.  Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD).

Authors:  Daniela Karall; Michaela Brunner-Krainz; Katharina Kogelnig; Vassiliki Konstantopoulou; Esther M Maier; Dorothea Möslinger; Barbara Plecko; Wolfgang Sperl; Barbara Volkmar; Sabine Scholl-Bürgi
Journal:  Orphanet J Rare Dis       Date:  2015-02-22       Impact factor: 4.123

9.  European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.

Authors:  Juliane Léger; Antonella Olivieri; Malcolm Donaldson; Toni Torresani; Heiko Krude; Guy van Vliet; Michel Polak; Gary Butler
Journal:  J Clin Endocrinol Metab       Date:  2014-01-21       Impact factor: 5.958

10.  Thyroid dysfunction in very low birth weight preterm infants.

Authors:  Ji Hoon Lee; Sung Woo Kim; Ga Won Jeon; Jong Beom Sin
Journal:  Korean J Pediatr       Date:  2015-06-22
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  2 in total

Review 1.  Impact of newborn screening on the reported incidence and clinical outcomes associated with medium- and long-chain fatty acid oxidation disorders.

Authors:  Deborah Marsden; Camille L Bedrosian; Jerry Vockley
Journal:  Genet Med       Date:  2021-01-25       Impact factor: 8.822

2.  The Disease Spectrum and Influencing Factors of NICU in Xiangxi, Underdeveloped Area of China: A 9-Year Retrospective Study.

Authors:  Fen Xie; Yuhua Zhu; Lulu Chen; Ruyi Han; Qingxia Shu; Zheng-Ying Chen; Jinxiu Li
Journal:  Front Pediatr       Date:  2022-06-17       Impact factor: 3.569

  2 in total

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