Evidence map›Paper›PMID 42455871›Full record

ArticlePLOS digital health2026

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

Pauline Scherdel, Raphaële Houlbracq, Emmanuel Lecoeur, Juliane Léger, Raja Brauner, Jérémie F Cohen, EBGM V Study Group, Martin Chalumeau, Barbara Heude

Abstract read
In one paragraph

Article in PLOS digital health, 2026. 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.

Pauline ScherdelUniversité Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Paris, France.ORCID https://orcid.org/0000-0003-4517-9430
Raphaële HoulbracqUniversité Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Paris, France.
Emmanuel LecoeurUniversité Paris Cité, Inserm, UMR1343, Pharmacologie et Évaluations des Thérapeutiques Chez l'enfant et la Femme Enceinte, Paris, France.
Juliane LégerDepartment of Pediatric Endocrinology and Diabetology, Robert-Debré Hospital, AP-HP, Université Paris Cité, Paris, France.
Raja BraunerUnité d'Endocrinologie Pédiatrique, Hôpital Fondation Adolphe de Rothschild, Paris, France.
Jérémie F CohenUniversité Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Paris, France.
EBGM V Study Group
Martin ChalumeauUniversité Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Paris, France.
Barbara HeudeUniversité Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our goal was to improve growth monitoring in children by developing and evaluating an artificial intelligence (AI) algorithm that can detect abnormal growth. We used pre-diagnosis height measurements for children with a diagnosis of growth hormone deficiency (GHD, n = 86) or Turner syndrome (TS, n = 87) in France (1990-2014) and all height measurements of apparently healthy children (referents, n = 923). We modeled the individual height growth curves by applying non-linear mixed models for each new measurement of each child. The resulting growth parameters were used in multinomial logistic regression across five pre-defined age ranges from 1 to 12 years to predict abnormal growth trajectories. For the five age-specific predictive models, we studied the discrimination and calibration curves, and retained the risk thresholds that offered a pre-defined specificity of 98%. Using all the available height measurements for cases and referents, we evaluated the cumulative diagnostic performance of the algorithm for detecting GHD or TS and the theoretical reduction in time to diagnosis. We evaluated these models internally using 5-fold cross-validation and externally from a regional sample of children with GHD (n = 77) or TS (n = 40) and a national sample of apparently healthy children (n = 5,755). The five age-specific predictive models had good discrimination (high AUROC range 0.87-0.99) and good calibration. Internal evaluations showed stable results. External evaluation revealed a cumulative sensitivity and specificity of 84.6% (95% CI 76.8-90.6) and 94.3% (93.6-94.9). The median theoretical reduction in time to diagnosis was 2.0 years (interquartile range 0.6-3.8): 1.6 years (0.5-2.8) for GHD and 3.0 years (1.0-5.4) for TS. To conclude, we developed and internally and externally evaluated an AI algorithm with high diagnostic performance for the early detection of GHD and TS. A refinement of the algorithm to include other target conditions and further external evaluation in other countries is needed before implementation in daily practice.

Identifiers

PMID42455871
PMCPMC13372244

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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.