Deep Learning-Based Automated Measurement of Murine Bone Length in Radiographs

Author:

Rong Ruichen1ORCID,Denton Kristin2,Jin Kevin W.1ORCID,Quan Peiran1,Wen Zhuoyu1ORCID,Kozlitina Julia3ORCID,Lyon Stephen4ORCID,Wang Aileen1,Wise Carol A.2356,Beutler Bruce4,Yang Donghan M.1ORCID,Li Qiwei7ORCID,Rios Jonathan J.23568ORCID,Xiao Guanghua189

Affiliation:

1. Quantitative Biomedical Research Center, Peter O’Donnell Jr. School of Public Health, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

2. Center for Pediatric Bone Biology and Translational Research, Scottish Rite for Children, Dallas, TX 75219, USA

3. McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

4. Center for the Genetics of Host Defense, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

5. Department of Orthopaedic Surgery, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

6. Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

7. Department of Mathematical Sciences, The University of Texas at Dallas, Richardson, TX 75083, USA

8. Simmons Comprehensive Cancer Center, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

9. Department of Bioinformatics, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

Abstract

Genetic mouse models of skeletal abnormalities have demonstrated promise in the identification of phenotypes relevant to human skeletal diseases. Traditionally, phenotypes are assessed by manually examining radiographs, a tedious and potentially error-prone process. In response, this study developed a deep learning-based model that streamlines the measurement of murine bone lengths from radiographs in an accurate and reproducible manner. A bone detection and measurement pipeline utilizing the Keypoint R-CNN algorithm with an EfficientNet-B3 feature extraction backbone was developed to detect murine bone positions and measure their lengths. The pipeline was developed utilizing 94 X-ray images with expert annotations on the start and end position of each murine bone. The accuracy of our pipeline was evaluated on an independent dataset test with 592 images, and further validated on a previously published dataset of 21,300 mouse radiographs. The results showed that our model performed comparably to humans in measuring tibia and femur lengths (R2 > 0.92, p-value = 0) and significantly outperformed humans in measuring pelvic lengths in terms of precision and consistency. Furthermore, the model improved the precision and consistency of genetic association mapping results, identifying significant associations between genetic mutations and skeletal phenotypes with reduced variability. This study demonstrates the feasibility and efficiency of automated murine bone length measurement in the identification of mouse models of abnormal skeletal phenotypes.

Funder

National Institutes of Health

Cancer Prevention and Research Institute of Texas

National Science Foundation

Scottish Rite for Children

Publisher

MDPI AG

Reference41 articles.

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