Development, internal and external evaluation of an artificial intelligence algorithm for child growth monitoring in

Pauline Scherdel1, Raphaële Houlbracq1, Emmanuel Lecoeur2,3

  • 1Université Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Paris, France.

PLOS Digital Health
|July 15, 2026
PubMed

Insights

An AI algorithm was developed to detect abnormal growth in children, potentially reducing diagnosis time for conditions like growth hormone deficiency (GHD) and Turner syndrome (TS). This AI tool shows high diagnostic performance, aiding early detection and improving pediatric growth monitoring.

Area of Science:

  • Pediatric Endocrinology
  • Medical Informatics
  • Artificial Intelligence in Healthcare

Background:

  • Accurate growth monitoring is crucial for identifying pediatric endocrine disorders.
  • Early detection of conditions like growth hormone deficiency (GHD) and Turner syndrome (TS) can significantly impact treatment outcomes.
  • Existing methods for growth monitoring may have limitations in early and accurate detection of abnormal growth trajectories.

Purpose of the Study:

  • To develop and evaluate an artificial intelligence (AI) algorithm for detecting abnormal growth patterns in children.
  • To assess the algorithm's diagnostic performance in identifying potential cases of GHD and TS.
  • To determine the potential reduction in time to diagnosis for these conditions using the AI algorithm.

Main Methods:

  • Utilized pre-diagnosis height measurements from children with GHD, TS, and healthy referents.
  • Applied non-linear mixed models to create individual height growth curves.
  • Employed multinomial logistic regression with age-specific models to predict abnormal growth trajectories.
  • Validated the AI algorithm through internal 5-fold cross-validation and external evaluations.

Main Results:

  • Developed five age-specific predictive models with high discrimination (AUROC 0.87-0.99) and good calibration.
  • External evaluation demonstrated a cumulative sensitivity of 84.6% and specificity of 94.3%.
  • The AI algorithm showed a median theoretical reduction in time to diagnosis of 2.0 years (1.6 years for GHD, 3.0 years for TS).

Conclusions:

  • The developed AI algorithm exhibits high diagnostic performance for the early detection of GHD and TS in children.
  • The AI tool has the potential to significantly shorten the time to diagnosis, enabling earlier intervention.
  • Further refinement and broader external validation are recommended before widespread clinical implementation.

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