Evidence map›Paper›PMID 40952600›Full record

ArticleJournal of endocrinological investigation2025

Newborn screening for congenital adrenal hyperplasia due to 21 hydroxylase deficiency: the Italian experience 2006-2019.

Federico Baronio, Enrica Abrigo, Sara Azzolini, Paolo Cavarzere, Cristina Cereda, Luisa De Sanctis, Silvia Laura Carla Meroni, Jessica Munarin, Francesca Righetti, Gianni Russo and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of endocrinological investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Federico BaronioDepartment Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna, Endo-ERN Center for Rare Endocrine Conditions, Bologna, Italy. federico.baronio@aosp.bo.it.ORCID http://orcid.org/0000-0003-3470-6880
Enrica AbrigoPediatric Endocrinology, Department of Public Health and Pediatrics, Regina Margherita Childrens'Hospital, University of Torino, Endo-ERN Center for Rare Endocrine Conditions, Torino, Italy.
Sara AzzoliniPediatric Division, Department of Pediatrics, University Hospital of Verona, Verona, Italy.
Paolo CavarzerePediatric Division, Department of Pediatrics, University Hospital of Verona, Verona, Italy.
Cristina CeredaCenter of Functional Genomics and Rare Diseases, Department of Pediatrics, Buzzi Children's Hospital, Milan, Italy.
Luisa De SanctisPediatric Endocrinology, Department of Public Health and Pediatrics, Regina Margherita Childrens'Hospital, University of Torino, Endo-ERN Center for Rare Endocrine Conditions, Torino, Italy.
Silvia Laura Carla MeroniDepartment of Pediatrics, Endocrine Unit, Scientific Institute San Raffaele, Endo-ERN Center for Rare Endocrine Conditions, Milan, Italy.
Jessica MunarinPediatric Endocrinology, Department of Public Health and Pediatrics, Regina Margherita Childrens'Hospital, University of Torino, Endo-ERN Center for Rare Endocrine Conditions, Torino, Italy.
Francesca RighettiDepartment Hospital of Woman and Child, Regional Laboratory for Neonatal Screening and Endocrine-Metabolic Diseases, IRCCS AOU di Bologna, Bologna, Italy.
Gianni RussoDepartment of Pediatrics, Endocrine Unit, Scientific Institute San Raffaele, Endo-ERN Center for Rare Endocrine Conditions, Milan, Italy.
Francesca TeofoliPediatric Section, Department Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
Antonio BalsamoDepartment Hospital of Woman and Child, Pediatric Unit, IRCCS AOU di Bologna, Endo-ERN Center for Rare Endocrine Conditions, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEarly identification of classic 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia (21OH-CAH) through newborn screening (NBS) is vital to prevent morbidity from salt-wasting crises. The aim of the study is to assess the efficacy of 21OH-CAH NBS from 2006 to 2019 in the five Regions of Italy where 21OH-CAH NBS is performed.

methodsMethods included dried blood spot (DBS) tests for 17OH-progesterone (17OHP) within the first 48-72 h, with variable protocols. Dried blood spots have been screened with a time-resolved fluoroimmunoassay for 17OHP determination (DELFIA) as first tier test in all the Italian Regions. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was implemented in the Veneto region starting October 2017 as second-tier test.

resultsAmong 2,933,074 screened newborns, 161 (86 males, 75 females) had classic 21OH-CAH, with a cumulative incidence of 1 in 17,699. Salt-wasting CAH was the most prevalent form (71.9%). Mean age at blood sampling for true positives was 9 ± 18 days, with 28% suspected before NBS results. In Regions with a second-tier test, the recall rate (RR) was 0.17, and positive predictive value (PPV) was 4.3. No patients had adrenal crisis and 23% of cases were symptomatic before the NBS results were reported.

conclusionsThe study confirms the efficacy of NBS in early detection of classic 21OH-CAH, emphasizing the need for timely reporting and second-tier testing to improve outcomes.

Indexed as

17-alpha-HydroxyprogesteroneAdrenal Hyperplasia, CongenitalNeonatal ScreeningDried Blood Spot TestingFemaleHumansInfant, NewbornItalyMaleTandem Mass Spectrometry17-alpha-Hydroxyprogesterone17-hydroxyprogesterone21 hydroxylase deficiencyCongenital adrenal hyperplasiaNewbornsNewborn screeningSalt wasting

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.