Persistent homology analysis distinguishes pathological bone microstructure in non-linear microscopy images

• Published in: Scientific reports Vol. 13; no. 1; p. 2522
• Main Authors: Pritchard, Ysanne, Sharma, Aikta, Clarkin, Claire, Ogden, Helen, Mahajan, Sumeet, Sánchez-García, Rubén J
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 13.02.2023; Nature Publishing Group UK; Nature Portfolio
• Subjects: Animal models; Animals; Bone and Bones - diagnostic imaging; Collagen; Female; Fibrillar Collagens; Homology; Male; Mice; Microscopy; Osteocalcin; Photons; Porosity; Statistical analysis; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-28985-3

We present a topological method for the detection and quantification of bone microstructure from non-linear microscopy images. Specifically, we analyse second harmonic generation (SHG) and two photon excited autofluorescence (TPaF) images of bone tissue which capture the distribution of matrix (fibrillar collagen) structure and autofluorescent molecules, respectively. Using persistent homology statistics with a signed Euclidean distance transform filtration on binary patches of images, we are able to quantify the number, size, distribution, and crowding of holes within and across samples imaged at the microscale. We apply our methodology to a previously characterized murine model of skeletal pathology whereby vascular endothelial growth factor expression was deleted in osteocalcin-expressing cells (OcnVEGFKO) presenting increased cortical porosity, compared to wild type (WT) littermate controls. We show significant differences in topological statistics between the OcnVEGFKO and WT groups and, when classifying the males, or females respectively, into OcnVEGFKO or WT groups, we obtain high prediction accuracies of 98.7% (74.2%) and 77.8% (65.8%) respectively for SHG (TPaF) images. The persistence statistics that we use are fully interpretable, can highlight regions of abnormality within an image and identify features at different spatial scales.