C. Hoemann (Manassas, US)

George Mason University Bioengineering
Dr. Hoemann is a full professor of Bioengineering at George Mason University in Virginia; USA. Her research program is developing new tools for the diagnosis and treatment of symptomatic early arthritis. Her training in biochemistry and molecular-cell biology (PhD; Massachusetts Institute of Technology) was followed by bench-to-bedside development of a biomaterial-based medical device for articular cartilage repair; BST-CarGel. This device incorporates chitosan; a naturally-derived polysaccharide polymer; into the patient’s own peripheral blood to create a “tissue engineered blood clot”. Her research is helping build a new paradigm that treats the blood clot as a living tissue whose bioresponses can be tuned by environmental cues. Dr. Hoemann is an honorary member of the International Cartilage Repair Society and fellow of International Orthopaedic Research (FIOR); serves on the editorial boards of Cartilage; OsteoArthritis & Cartilage Open; is a co-founder of Ortho RTi; and internationally recognized for her expertise in orthopaedics; biomaterials; and inflammation. Her particular areas of focus include the cartilage-bone interface; osteogenesis; chondroinduction; and how subchondral bone fracture repair responses are guided by the presence of different types of structural and soluble biomaterials. Through bioengineering and clinical collaborations; she is using high frequency ultrasound to advance a new theory of creeping mineralization of articular cartilage; or tidemark advancement; after post-traumatic knee injury.

Presenter Of 1 Presentation

Poster Cartilage Imaging and Functional Testing

P012 - Development of a Novel Quantitative Ultrasound Parameter to Measure Tidemark Remodeling

Presentation Topic
Cartilage Imaging and Functional Testing
Date
13.04.2022
Lecture Time
09:30 - 09:30
Room
Exhibition Foyer
Session Name
7.3 - Poster Viewing / Coffee Break / Exhibition
Session Type
Poster Session
Disclosure
C.D. Hoemann, Ortho RTi, shareholder, Scientific Advisoary Board. All other authors: No significant relationship.

Abstract

Purpose

Traumatic joint injury can initiate osteoarthritis and launch a slow process of creeping mineralization and tidemark advancement through unclear mechanisms. High-frequency ultrasound is a non-destructive approach that can be used to image the cartilage-bone interface. The purpose of this study was to develop a novel quantitative ultrasound (QUS) parameter that reflects alterations in tidemark structure due to changes in mineralization.

Methods and Materials

Osteochondral explants 3mm in diameter were extracted with 8G Jamshidi needles from an adult bovine shoulder (N=1) or intact human knee cartilage (N=3, de-identified arthroplasty surgical waste). Explants were cultured in vitro, fixed and decalcified in EDTA. Specimens were SAM scanned by raster-scanning a 15 MHz transducer (Olympus) at the optimal focal length of 50.8 in a 6x6mm grid at 100 µm steps. A log-compressed envelope signal (dB per mm) in a 1 mm2 area in the center of each explant was produced (MATLAB). The QUS alpha parameter was defined as the slope (dB/mm) between the maximal subchondral signal and 200 µm prior. Differences were evaluated by matched pair design (JMP-Pro, significance set at p˂0.05).

Results

Osteochondral SAM scans produced two prominent signals along the scanning axis at the articular cartilage surface and the tidemark (Fig. 1A), as previously reported by others. We report the novel finding that decalcification altered the echogenic backscatter at the tidemark, with increased echogenicity in subchondral bone (Fig. 1B). Compared to healthy bovine tissue, human OA articular cartilage was thicker, produced more backscatter inside the articular cartilage, showed higher alpha values, and required longer decalcification times to observe changes in alpha.

fig1(1).jpg

Conclusion

A high alpha indicates a rapid spatial increase in echogenicity that is expected for a well-developed and intact mature tidemark. Tidemark advancement produces a hypomineralized tissue suggesting that QUS could be useful for identifying longitudinal changes in the tidemark, in an explant model.

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Presenter Of 1 Presentation

Cartilage Imaging and Functional Testing

P012 - Development of a Novel Quantitative Ultrasound Parameter to Measure Tidemark Remodeling

Abstract

Purpose

Traumatic joint injury can initiate osteoarthritis and launch a slow process of creeping mineralization and tidemark advancement through unclear mechanisms. High-frequency ultrasound is a non-destructive approach that can be used to image the cartilage-bone interface. The purpose of this study was to develop a novel quantitative ultrasound (QUS) parameter that reflects alterations in tidemark structure due to changes in mineralization.

Methods and Materials

Osteochondral explants 3mm in diameter were extracted with 8G Jamshidi needles from an adult bovine shoulder (N=1) or intact human knee cartilage (N=3, de-identified arthroplasty surgical waste). Explants were cultured in vitro, fixed and decalcified in EDTA. Specimens were SAM scanned by raster-scanning a 15 MHz transducer (Olympus) at the optimal focal length of 50.8 in a 6x6mm grid at 100 µm steps. A log-compressed envelope signal (dB per mm) in a 1 mm2 area in the center of each explant was produced (MATLAB). The QUS alpha parameter was defined as the slope (dB/mm) between the maximal subchondral signal and 200 µm prior. Differences were evaluated by matched pair design (JMP-Pro, significance set at p˂0.05).

Results

Osteochondral SAM scans produced two prominent signals along the scanning axis at the articular cartilage surface and the tidemark (Fig. 1A), as previously reported by others. We report the novel finding that decalcification altered the echogenic backscatter at the tidemark, with increased echogenicity in subchondral bone (Fig. 1B). Compared to healthy bovine tissue, human OA articular cartilage was thicker, produced more backscatter inside the articular cartilage, showed higher alpha values, and required longer decalcification times to observe changes in alpha.

fig1(1).jpg

Conclusion

A high alpha indicates a rapid spatial increase in echogenicity that is expected for a well-developed and intact mature tidemark. Tidemark advancement produces a hypomineralized tissue suggesting that QUS could be useful for identifying longitudinal changes in the tidemark, in an explant model.

Collapse