[Neonatal screening for cystic fibrosis in the Liège region : first evaluation after 4 years].

Since January 2020, neonatal screening for cystic fibrosis (CF-NBS) has been implemented in the Wallonia-Brussels Federation. It's based on the immunoreactive trypsin (IRT1) assay between day 2 and day 4, associated with a 12 CFTR pathogenic variants analysis and with an IRT control on day 21. The aim of this study is to evaluate the performance of our CF-NBS in Liège according to the quality criteria defined by the European Cystic Fibrosis Society's working group on neonatal screening. After four years, 58.762 newborns have been screened. Nineteen children with cystic fibrosis were diagnosed : 14 by NBS, 3 following a meconium ileus, 1 by family history and 1 false negative diagnosed on clinical basis. Furthermore, 39 healthy carriers and 2 uncertain diagnosis (CFSPID) were identified. The sensitivity of CF NBS is 93,3 % (target ≥ 95 %), the positive predictive value (PPV) 17,7 % (target ≥ 30 %). Increasing the TIR1 threshold by 0,1 in 0,1 from P99 to P99,5, would be associated with a lower sensitivity and a non-significant improvement of PPV. A national assessment of CF NBS needs to be carried out.

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PubMed
Published
2024-10-01
Primary Topic
Cystic Fibrosis Research Advances
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article
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article

[Neonatal screening for cystic fibrosis in the Liège region : first evaluation after 4 years].

Vinciane Dideberg, Hedwige Boboli, Matthieu Thimmesch, Géraldine Luis et al.
PubMed
Cystic Fibrosis Research Advances
article

[Neonatal screening for cystic fibrosis in the Liège region : first evaluation after 4 years].

Vinciane Dideberg, Hedwige Boboli, Matthieu Thimmesch, Géraldine Luis, Cécile Libioulle, François Boemer
article en

Abstract

Since January 2020, neonatal screening for cystic fibrosis (CF-NBS) has been implemented in the Wallonia-Brussels Federation. It's based on the immunoreactive trypsin (IRT1) assay between day 2 and day 4, associated with a 12 CFTR pathogenic variants analysis and with an IRT control on day 21. The aim of this study is to evaluate the performance of our CF-NBS in Liège according to the quality criteria defined by the European Cystic Fibrosis Society's working group on neonatal screening. After four years, 58.762 newborns have been screened. Nineteen children with cystic fibrosis were diagnosed : 14 by NBS, 3 following a meconium ileus, 1 by family history and 1 false negative diagnosed on clinical basis. Furthermore, 39 healthy carriers and 2 uncertain diagnosis (CFSPID) were identified. The sensitivity of CF NBS is 93,3 % (target ≥ 95 %), the positive predictive value (PPV) 17,7 % (target ≥ 30 %). Increasing the TIR1 threshold by 0,1 in 0,1 from P99 to P99,5, would be associated with a lower sensitivity and a non-significant improvement of PPV. A national assessment of CF NBS needs to be carried out.

PubMedVol. 79(10)
Centre Hospitalier Chrétien (BE), Département Génétique Animale (FR), Centre Hospitalier Universitaire de Liège (BE), Laboratoire de Génétique Cellulaire (FR), Génétique Médicale & Génomique Fonctionelle (FR)
Cystic Fibrosis Research Advances
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[Neonatal screening for cystic fibrosis in the Liège region : first evaluation after 4 years]. — Vinciane Dideberg, Hedwige Boboli, et al. · PubMed (2024) | TGRS Research Map | TGRS