Evidence map›Paper›PMID 37752373›Full record

ArticleJournal of endocrinological investigation2024

The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.

G I Baroncelli, G Carlucci, E Freri, M R Giuca, V Guarnieri, G Navarra, B Toschi, S Mora

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Journal of endocrinological investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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, 8 citations in OpenAlex.

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

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

G I BaroncelliPediatric and Adolescent Endocrinology, Division of Pediatrics, Department of Obstetrics, Gynecology and Pediatrics, University Hospital, Pisa, Italy.ORCID http://orcid.org/0000-0001-8465-5087
G CarlucciOPT S.P.A., Soluzioni Per Il Mondo Healthcare, Milan, Italy.
E FreriDepartment of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID http://orcid.org/0000-0002-2293-8687
M R GiucaUnit of Pediatric Dentistry, Department of Surgical Medical Molecular Pathology and Critical Area, Dental and Oral Surgery Clinic, University of Pisa, Pisa, Italy.ORCID http://orcid.org/0000-0002-4575-9761
V GuarnieriDivision of Medical Genetics, Fondazione IRCCS Casa Sollievo della Sofferenza, Foggia, Italy.ORCID http://orcid.org/0000-0002-5500-8558
G NavarraOPT S.P.A., Soluzioni Per Il Mondo Healthcare, Milan, Italy.
B ToschiSection of Medical Genetics, Department of Medical and Oncological Area, University Hospital, Pisa, Italy.ORCID http://orcid.org/0000-0003-4193-4128
S MoraLaboratory of Pediatric Endocrinology, Department of Pediatrics, IRCCS San Raffaele Hospital, Milan, Italy. mora.stefano@hsr.it.ORCID http://orcid.org/0000-0002-4781-6715
Azienda Ospedaliera Universitaria Pisana · ITCasa Sollievo della Sofferenza · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Pisa · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypophosphatasia (HPP) is a rare genetic disorder in which pathogenic variants of the ALPL gene lead to a marked decrease of tissue non-specific alkaline phosphatase (TNSALP) activity. Although HPP is a systemic disorder, its clinical manifestations are more evident on bones, teeth, muscle and central nervous system. The clinical spectrum ranges from severe forms with extreme skeletal deformities, respiratory impairment, seizures, to very mild forms with onset in late adulthood and few clinical signs. The diagnosis can be suspected by measurement of TNSALP activity, but the insufficient awareness among health professionals and the lack of official guidelines are responsible for delayed diagnosis in children with HPP. The purpose of the current document is to provide an expert opinion directed at optimizing the diagnostic pathway of pediatric HPP. From April to December 2022, a multidisciplinary working group of 6 experts including two pediatric endocrinologists, a pediatric neurologist, a pediatric odontologist, a clinical geneticist, and a molecular biologist gathered in a series of periodic meetings to discuss the main issues related to the diagnosis of HPP in children and formalize an Expert Opinion statement. The experts agreed on a diagnostic trail that begins with the recognition of specific clinical signs, leading to biochemical analyses of TNSALP activity and vitamin B6 serum concentration. Very important are the neurological and dental manifestation of the disease that should be thoroughly investigated. The evaluation of TNSALP activity must consider sex and age variability and low activity must be persistent. Repeated blood measurements are thus necessary. The molecular analysis is then mandatory to confirm the diagnosis and for genetic counseling.

Indexed as

HypophosphatasiaRespiratory InsufficiencyAdultAlkaline PhosphataseCentral Nervous SystemChildHealth PersonnelHumansMutationAlkaline Phosphatase

Identifiers

PMID37752373
PMCPMC10904512
OpenAlexW4387037810

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.