Clinical validation of a deep-learning-based bone age software in healthy Korean children.

IF 2.8 Q3 ENDOCRINOLOGY & METABOLISM Annals of Pediatric Endocrinology & Metabolism Pub Date : 2024-04-01 Epub Date: 2024-01-24 DOI:10.6065/apem.2346050.025
Hyo-Kyoung Nam, Winnah Wu-In Lea, Zepa Yang, Eunjin Noh, Young-Jun Rhie, Kee-Hyoung Lee, Suk-Joo Hong
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Abstract

Purpose: Bone age (BA) is needed to assess developmental status and growth disorders. We evaluated the clinical performance of a deep-learning-based BA software to estimate the chronological age (CA) of healthy Korean children.

Methods: This retrospective study included 371 healthy children (217 boys, 154 girls), aged between 4 and 17 years, who visited the Department of Pediatrics for health check-ups between January 2017 and December 2018. A total of 553 left-hand radiographs from 371 healthy Korean children were evaluated using a commercial deep-learning-based BA software (BoneAge, Vuno, Seoul, Korea). The clinical performance of the deep learning (DL) software was determined using the concordance rate and Bland-Altman analysis via comparison with the CA.

Results: A 2-sample t-test (P<0.001) and Fisher exact test (P=0.011) showed a significant difference between the normal CA and the BA estimated by the DL software. There was good correlation between the 2 variables (r=0.96, P<0.001); however, the root mean square error was 15.4 months. With a 12-month cutoff, the concordance rate was 58.8%. The Bland-Altman plot showed that the DL software tended to underestimate the BA compared with the CA, especially in children under the age of 8.3 years.

Conclusion: The DL-based BA software showed a low concordance rate and a tendency to underestimate the BA in healthy Korean children.

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基于深度学习的骨龄软件在韩国健康儿童身上的临床验证。
目的:评估发育状况和生长障碍需要骨龄。我们的目的是评估基于深度学习的骨龄软件对韩国健康儿童年代年龄的临床表现:这项回顾性研究纳入了2017年1月至2018年12月期间到儿科进行健康检查的371名健康儿童(217名男孩,154名女孩),年龄在4岁至17岁之间。研究人员使用基于深度学习的商用骨龄软件(BoneAge,Vuno,韩国首尔)对 371 名健康韩国儿童的共计 553 张左手X光片进行了评估。深度学习软件的临床性能是通过与年代年龄的比较,使用一致率和布兰德-阿尔特曼分析来确定的:双样本 t 检验(P < 0.001)和费雪精确检验(P = 0.011)显示,正常年代年龄与深度学习软件估计的骨龄之间存在显著差异。这两个变量之间存在良好的相关性(r = 0.96,P < 0.001);然而,均方根误差为 15.4 个月。以 12 个月为分界线,吻合率为 58.8%。布兰-阿尔特曼图显示,与年代年龄相比,深度学习软件倾向于低估骨龄,尤其是8.3岁以下的儿童:基于深度学习的骨龄软件在韩国健康儿童中显示出较低的一致性和低估骨龄的倾向。
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来源期刊
CiteScore
4.00
自引率
18.20%
发文量
59
审稿时长
24 weeks
期刊介绍: The Annals of Pediatric Endocrinology & Metabolism Journal is the official publication of the Korean Society of Pediatric Endocrinology. Its formal abbreviated title is “Ann Pediatr Endocrinol Metab”. It is a peer-reviewed open access journal of medicine published in English. The journal was launched in 1996 under the title of ‘Journal of Korean Society of Pediatric Endocrinology’ until 2011 (pISSN 1226-2242). Since 2012, the title is now changed to ‘Annals of Pediatric Endocrinology & Metabolism’. The Journal is published four times per year on the last day of March, June, September, and December. It is widely distributed for free to members of the Korean Society of Pediatric Endocrinology, medical schools, libraries, and academic institutions. The journal is indexed/tracked/covered by web sites of PubMed Central, PubMed, Emerging Sources Citation Index (ESCI), Scopus, EBSCO, EMBASE, KoreaMed, KoMCI, KCI, Science Central, DOI/CrossRef, Directory of Open Access Journals(DOAJ), and Google Scholar. The aims of Annals of Pediatric Endocrinology & Metabolism are to contribute to the advancements in the fields of pediatric endocrinology & metabolism through the scientific reviews and interchange of all of pediatric endocrinology and metabolism. It aims to reflect the latest clinical, translational, and basic research trends from worldwide valuable achievements. In addition, genome research, epidemiology, public education and clinical practice guidelines in each country are welcomed for publication. The Journal particularly focuses on research conducted with Asian-Pacific children whose genetic and environmental backgrounds are different from those of the Western. Area of specific interest include the following : Growth, puberty, glucose metabolism including diabetes mellitus, obesity, nutrition, disorders of sexual development, pituitary, thyroid, parathyroid, adrenal cortex, bone or other endocrine and metabolic disorders from infancy through adolescence.
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