Impact of Pancreatitis-Associated Protein on Newborn Screening Outcomes and Detection of CFTR-Related Metabolic Syndrome (CRMS)/Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A Monocentric Prospective Pilot Experience.

PAP PPV outcomes screening sweat chloride

Journal

International journal of neonatal screening
ISSN: 2409-515X
Titre abrégé: Int J Neonatal Screen
Pays: Switzerland
ID NLM: 101665400

Informations de publication

Date de publication:
03 Aug 2022
Historique:
received: 21 06 2022
revised: 14 07 2022
accepted: 29 07 2022
entrez: 23 8 2022
pubmed: 24 8 2022
medline: 24 8 2022
Statut: epublish

Résumé

Pancreatitis-Associated Protein (PAP)-based Cystic Fibrosis (CF) newborn bloodspot screening (NBS) protocols detect less CFTR-Related Metabolic Syndrome (CRMS)/CF Screen Positive, Inconclusive Diagnosis (CFSPID). We prospectively evaluated the impact of PAP as the second step of the CF NBS protocol, before the CFTR genetic analysis, on NBS outcomes and CRMS/CFSPID detection in the Tuscany region, Italy. In parallel to the usual protocol (IRT/DNA, protocol 1), PAP was analyzed in IRT-positive infants (IRT/PAP/DNA, protocol 2) from 1 June 2020 until 31 May 2022. We defined an infant as NBS positive if PAP was >1.8 μg/L for IRT value 99th percentile-100 μg/L or >0.6 μg/L for IRT value >100 μg/L. To increase the positive predictive value (PPV) of protocol 2, we retrospectively lowered the upper IRT range value from 100 to 90 μg/L (modified protocol 2). We identified 8 CF and 13 CRMS/CFSPID with protocol 1, 5 CF and 5 CRMS/CFSPID with protocol 2 and 8 CF and 5 CRMS/CFSPID with modified protocol 2. With the PAP-based protocols, we observed a reduction of sweat tests, healthy carrier detection and a significant increase in PPV to 15.38%. Further data are needed in order to evaluate the outcomes of CRMS/CFSPID after a long follow-up.

Identifiants

pubmed: 35997436
pii: ijns8030046
doi: 10.3390/ijns8030046
pmc: PMC9397086
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Tuscany Region
ID : K36

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Auteurs

Chiara Bianchimani (C)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Daniela Dolce (D)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Claudia Centrone (C)

Diagnostic Genetics Unit, Careggi University Hospital, 50139 Florence, Italy.

Silvia Campana (S)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Novella Ravenni (N)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Tommaso Orioli (T)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Erica Camera (E)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Gianfranco Mergni (G)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Cristina Fevola (C)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Paolo Bonomi (P)

Freelance Statistician, 20100 Milan, Italy.

Giovanni Taccetti (G)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Vito Terlizzi (V)

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Classifications MeSH