Evidence map›Paper›PMID 40555852›Full record

ArticleEuropean journal of pediatrics2025

Insulin-like growth factor 1 as a diagnostic marker of progressive central precocious puberty: a prospective study.

Ana Luísa Leite, Luís Filipe Azevedo, Rosa Arménia Campos, Maria Adriana Rangel, Clara Torres, Filipa Marques Santos, Sónia Aires, João Firmino-Machado, Catarina Limbert

Abstract read
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Ana Luísa LeiteUnit of Paediatric Endocrinology and Diabetes, Department of Paediatrics, Unidade Local de Saúde Gaia e Espinho, Vila Nova de Gaia, Portugal. ana.leite@ulsge.min-saude.pt.ORCID http://orcid.org/0000-0003-2616-5324
Luís Filipe AzevedoDepartment of Community Medicine, Information and Health Decision Sciences (MEDCIDS), Faculty of Medicine, University of Porto, Porto, Portugal.ORCID http://orcid.org/0000-0002-8421-2937
Rosa Arménia CamposUnit of Paediatric Endocrinology and Diabetes, Department of Paediatrics, Unidade Local de Saúde Gaia e Espinho, Vila Nova de Gaia, Portugal.ORCID http://orcid.org/0000-0002-6654-4460
Maria Adriana RangelUnit of Paediatric Endocrinology and Diabetes, Department of Paediatrics, Unidade Local de Saúde Gaia e Espinho, Vila Nova de Gaia, Portugal.ORCID http://orcid.org/0000-0002-6130-2446
Clara TorresDepartment of Medical Sciences, University of Aveiro, Aveiro, Portugal.ORCID http://orcid.org/0009-0005-7385-8694
Filipa Marques SantosDepartment of Medical Sciences, University of Aveiro, Aveiro, Portugal.ORCID http://orcid.org/0000-0002-5791-719X
Sónia AiresDepartment of Medical Sciences, University of Aveiro, Aveiro, Portugal.ORCID http://orcid.org/0009-0001-2574-3180
João Firmino-MachadoDepartment of Medical Sciences, University of Aveiro, Aveiro, Portugal.ORCID http://orcid.org/0000-0001-9410-633X
Catarina LimbertUnit of Paediatric Endocrinology and Diabetes, Hospital Dona Estefânia, Lisbon, Portugal.ORCID http://orcid.org/0000-0002-7455-4538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Central precocious puberty (CPP) diagnosis often requires invasive GnRH stimulation tests. Our purpose was to determine whether the IGF-1 and IGF-1 SDSs are reliable predictors of progressive CPP. This was a prospective study including 82 girls under 8 years of age. The participants were divided into CPP (n = 39), NP-CPP and IT (n = 26), and control groups (n = 17). Anthropometric measurements, Tanner staging, bone age, pelvic ultrasound, and serum IGF1 and IGF1-SDS level measurements were performed. GnRH stimulation tests confirmed CPP cases. The mean IGF1 and IGF1-SDS levels were significantly greater in CPP patients (270.15 ng/mL; 1.943 SDS) than in NP-CPP patients (174.12 ng/mL; 0.788 SDS) and controls (139.28 ng/mL; 0.208 SDS) (p < 0.001). Multivariate logistic regression analysis confirmed that IGF1 (OR = 1.025, 95% CI 1.010-1.040) and IGF1-SDS (OR = 8.721, 95% CI 2.624-28.986) were significant predictors of CPP. ROC analysis revealed an AUC of 0.837 for IGF1 (95% CI 0.738-0.935) and 0.862 for IGF1-SDS (95% CI 0.771-0.953). The cut-off values of 231 ng/mL for IGF1 (71.8% sensitivity, 97.7% specificity) and 1.44 for IGF1-SDS (79.5% sensitivity, 90.7% specificity) demonstrated good accuracy (82.2% and 77.8%, respectively).

conclusionIGF1-SDS, and absolute IGF1, are promising effective noninvasive diagnostic markers for distinguishing CPP from nonprogressive precocious puberty. Due to its high specificity IGF1 values above 1.44, SDS may significantly increase the post-test probability of CPP, potentially avoiding invasive GnRH stimulation tests. These findings support the integration of IGF1 measurements into the initial diagnostic approach for girls presenting with early pubertal signs. WHAT IS KNOWN: • Central precocious puberty (CPP) often requires invasive GnRH stimulation tests. • IGF1 levels rise during puberty and reflect growth and pubertal progression. WHAT IS NEW: • This prospective study suggests IGF1-SDS >1.44 as accurate cut-off for progressive CPP via the IMMULITE assay. • IGF1-SDS show high specificity and diagnostic accuracy, supporting its use in the initial diagnostic approach for girls presenting with early pubertal signs.

Indexed as

Insulin-Like Growth Factor IPuberty, PrecociousBiomarkersCase-Control StudiesChildChild, PreschoolFemaleHumansInsulin-Like PeptidesProspective StudiesROC CurveSensitivity and SpecificityBiomarkersIGF1 protein, humanInsulin-Like Growth Factor IInsulin-Like PeptidesCentral precocious pubertyIGF1-SDSInsulin-like growth factor 1

Identifiers

PMID40555852
PMCPMC12187815

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Registered trials

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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.