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

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

PMC · DOI: 10.1007/s00431-025-06276-5 · European Journal of Pediatrics · 2025-06-24

## TL;DR

This study shows that IGF1-SDS levels above 1.44 can help diagnose progressive early puberty in girls without needing invasive tests.

## Contribution

IGF1-SDS >1.44 is proposed as a noninvasive diagnostic marker for progressive central precocious puberty.

## Key findings

- IGF1-SDS levels were significantly higher in CPP patients compared to nonprogressive cases and controls.
- IGF1-SDS >1.44 showed high specificity and diagnostic accuracy for CPP.
- Using IGF1-SDS could reduce the need for invasive GnRH stimulation tests.

## 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). Conclusion: IGF1-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.

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.

## Linked entities

- **Proteins:** IGF1 (insulin like growth factor 1)
- **Diseases:** central precocious puberty (MONDO:0019165), CPP (MONDO:0009837)

## Full-text entities

- **Genes:** GNRH1 (gonadotropin releasing hormone 1) [NCBI Gene 2796] {aka GNRH, GRH, LHRH, LNRH}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}
- **Diseases:** CPP (MESH:D011629)
- **Chemicals:** SDS (MESH:D012967)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12187815/full.md

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Source: https://tomesphere.com/paper/PMC12187815