Evidence map›Paper›PMID 41890183›Full record

ArticleFrontiers in endocrinology2026

digiBONE: an automated tool for segmental Greulich-Pyle bone age assessment of Indian children and adolescents.

Shreya Chakladar, Chirantap Oza, Shruti Mondkar, Tim R J Aeppli, Lars Sävendahl, Anuradha Khadilkar, Vaman Khadilkar, Pranay Goel

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Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Shreya ChakladarDepartment of Biology, Indian Institute of Science Education and Research (IISER) Pune, Pune, India.
Chirantap OzaHirabai Cowasji Jehangir Medical Research Institute (HCJMRI), Pune, India.
Shruti MondkarHirabai Cowasji Jehangir Medical Research Institute (HCJMRI), Pune, India.
Tim R J AeppliDivision of Pediatric Endocrinology, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Lars SävendahlDivision of Pediatric Endocrinology, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Anuradha KhadilkarHirabai Cowasji Jehangir Medical Research Institute (HCJMRI), Pune, India.
Vaman KhadilkarHirabai Cowasji Jehangir Medical Research Institute (HCJMRI), Pune, India.
Pranay GoelDepartment of Biology, Indian Institute of Science Education and Research (IISER) Pune, Pune, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Accurate bone age assessment (BAA) is essential for diagnosing and managing pediatric endocrine and growth disorders, as it reflects biological maturity beyond chronological age. The widely used Greulich-Pyle (GP) method estimates bone age by visually comparing full-hand radiographs with standardised reference images. Although widely used, this technique-and most automated systems based on it-assumes uniform skeletal maturation across the hand. In practice, however, skeletal maturation progresses at different rates in the anatomical segments of the hand under varied hormonal influences. This segmental variability may contribute to inter-observer inconsistency and diagnostic uncertainty. We developed digiBONE, a deep learning framework that models segment-specific skeletal maturation. Methods: Hand radiographs were segmented into anatomically coherent regions-short bones, carpals, and wrist-representing synchronously maturing bones. Separate convolutional neural networks (CNNs) were trained for each segment and for the full hand. Segmental predictions were combined with the full-hand model to generate a composite bone age prediction. Results: Integration of segmental maturity improved performance over full-hand-only models, achieving mean absolute differences (MAD) of 4.75 months for boys and 4.93 months for girls. In addition to improved accuracy, it revealed asynchrony between hand regions providing complementary maturity information beyond global estimates. Discussion: The full-hand model captures how a child's overall maturity aligns with population norms, while, the segmental models explain how individuals of the same GP age differ biologically, improving interpretability and personalisation. digiBONE demonstrates that integrating biologically relevant segmental information into deep learning pipelines offers a scalable, automated bone age assessment solution applicable to Indian populations.

Indexed as

Age Determination by SkeletonDeep LearningHand BonesAdolescentBone DevelopmentChildChild, PreschoolConvolutional Neural NetworksFemaleHumansImage Processing, Computer-AssistedIndiaMalebone age assessmentcarpalsconvolutional neural networksfull-hand radiographsGreulich-Pylesegmental skeletal maturityshort boneswrist bones

Identifiers

PMID41890183
PMCPMC13012973

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