CARTILAGEPub Date : 2025-03-14DOI: 10.1177/19476035251316715
Mohammadhamed Shahsavari, Shannon Clark, Janet A W Elliott, Nadr M Jomha
{"title":"Successful Vitrification of Human Osteochondral Dowels and Intact Femoral Condyle.","authors":"Mohammadhamed Shahsavari, Shannon Clark, Janet A W Elliott, Nadr M Jomha","doi":"10.1177/19476035251316715","DOIUrl":"10.1177/19476035251316715","url":null,"abstract":"<p><p>ObjectiveCryopreservation via vitrification of articular cartilage (AC) will increase the availability of graft tissue for treating large joint defects. To advance this research area, we compared the effects of 2 cryopreservation protocols in which 10-mm diameter human osteochondral dowels were cooled and stored in liquid nitrogen vapor.DesignDowels collected from healthy human knee joints (<i>n</i> = 3 donors) of deceased donors were randomly assigned to Protocol 8 (430 min) or Protocol 2BWF (410 min). Post-warming chondrocyte viability was assessed and normalized to fresh controls.ResultsBoth protocols resulted in high chondrocyte viability after loading, vitrification, and rewarming (~80% of fresh control). Protocol 2BWF was subsequently used to vitrify and rewarm 3 human intact lateral femoral condyles. After rewarming, metabolic activity, normalized chondrocyte viability, histology, and matrix productivity were experimentally measured. Results documented ~82% of fresh chondrocyte viability post vitrification and rewarming, with similar results to the fresh control group on the other AC quality criteria.ConclusionThese results demonstrate that both Protocol 8 and Protocol 2BWF can preserve the quality of vitrified human AC in osteochondral dowels and human intact femoral condyles.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"19476035251316715"},"PeriodicalIF":2.7,"publicationDate":"2025-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11909651/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143623587","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
CARTILAGEPub Date : 2025-03-12DOI: 10.1177/19476035241301294
Alena Richter, Anna Altemeier, Christoph Becher, Marco Güllmann, Christian Plaass, Sarah Ettinger
{"title":"Influence of the BMI (<30 kg/m<sup>2</sup> vs. ≥30 kg/m<sup>2</sup>) on the Surgical Outcome of Osteochondral Lesions of the Talus: Prospective Data from the German Cartilage Registry (KnorpelRegister DGOU).","authors":"Alena Richter, Anna Altemeier, Christoph Becher, Marco Güllmann, Christian Plaass, Sarah Ettinger","doi":"10.1177/19476035241301294","DOIUrl":"10.1177/19476035241301294","url":null,"abstract":"<p><p>ObjectiveAim of this study was to evaluate the 24 months follow-up data of the German Cartilage Registry (KnorpelRegister DGOU, GCR) regarding the influence of body mass index (BMI) on clinical outcomes after surgical osteochondral lesions of the talus (OCT) treatment.DesignA total of 303 patients met the inclusion criteria. Pre- and post-operative Foot and Ankle Outcome Score (FAOS) total scores, subscores, and ΔFAOS were analyzed for most frequent surgical techniques (bone marrow stimulation [BMS], matrix-augmented BMS, matrix-augmented BMS with additional bone grafting) in normal weight group (NW, BMI <30 kg/m<sup>2</sup>, <i>n</i> = 228) and obese weight group (OW, BMI ≥30 kg/m<sup>2</sup>, <i>n</i> = 75).ResultsBMI was significantly different in NW and OW (24.6 ± 2.97 [16.9-29.9] kg/m<sup>2</sup> vs. 33.7 ± 4.0 [30.0-51.3] kg/m<sup>2</sup>, <i>P</i> < 0.001). Significant improvement from pre- to post-operative FAOS score and subscales was reached in both groups (NW: 64.2 ± 17.5 vs. 77.7 ± 17.8; OW: 52.3 ± 15.5 vs. 73.5 ± 20.2; <i>P</i> < 0.001) with higher pre- and post-operative scores in NW. No significant difference in ΔFAOS score was detected. Treatment technique did not influence the clinical outcome. OW showed an extended use of bone grafting due to greater defect depth. Age was significantly higher in OW compared to NW (35.7 ± 13.2 [18.0-69.0] years vs. 40.7 ± 13.1 [18.0-77.0] years, <i>P</i> = 0.005).ConclusionsPatients benefit from surgical cartilage therapy regardless of their BMI. OW showed significantly lower pre- and post-operative FAOS scores. In OW, additional bone grafting was required more frequently due to significantly deeper defects.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"19476035241301294"},"PeriodicalIF":2.7,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11907501/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143603990","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
CARTILAGEPub Date : 2025-03-01Epub Date: 2023-09-15DOI: 10.1177/19476035231196224
Fei Xiong, Yan Chevalier, Roland M Klar
{"title":"Parallel Chondrogenesis and Osteogenesis Tissue Morphogenesis in Muscle Tissue via Combinations of TGF-β Supergene Family Members.","authors":"Fei Xiong, Yan Chevalier, Roland M Klar","doi":"10.1177/19476035231196224","DOIUrl":"10.1177/19476035231196224","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to decipher the temporal and spatial signaling code for clinical cartilage and bone regeneration. We investigated the effects of continuous equal dosages of a single, dual, or triplicate growth factor combination of bone morphogenetic protein (BMP)-2, transforming growth factor (TGF)-β3, and/or BMP-7 on muscle tissue over a culturing period. The hypothesis was that specific growth factor combinations at specific time points direct tissue transformation toward endochondral bone or cartilage formation.</p><p><strong>Design: </strong>The harvested muscle tissues from F-344 adult male rats were cultured in 96-well plates maintained in a specific medium and cultured at specific conditions. And the multidimensional and multi-time point analyses were performed at both the genetic and protein levels.</p><p><strong>Results: </strong>The results insinuate that the application of growth factor stimulates a chaotic tissue response that does not follow a chronological signaling cascade. Both osteogenic and chondrogenic genes showed upregulation after induction, a similar result was also observed in the semiquantitative analysis after immunohistochemical staining against different antigens.</p><p><strong>Conclusions: </strong>The study showed that multiple TGF-β superfamily proteins applied to tissue stimulate developmental tissue processes that do not follow current tissue formation rules. The findings contribute to the understanding of the chronological order of signals and expression patterns needed to achieve chondrogenesis, articular chondrogenesis, or osteogenesis, which is crucial for the development of treatments that can regrow bone and articular cartilage clinically.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"71-88"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11744598/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10264117","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Ultra-Short Echo Time-MRI T2* Mapping of Articular Cartilage Layers Is Associated with Histological Early Degeneration.","authors":"Rui Imamura, Atsushi Teramoto, Yasutaka Murahashi, Yohei Okada, Shinichiro Okimura, Yoshihiro Akatsuka, Kota Watanabe, Toshihiko Yamashita","doi":"10.1177/19476035231205685","DOIUrl":"10.1177/19476035231205685","url":null,"abstract":"<p><strong>Objective: </strong>Ultra-short TE (UTE) sequences on MRI are a technique that improves the visualization of tissues with short T2 relaxation time, such as deep cartilage layers. In addition, T2* relaxation time calculated from the UTE has the potential to evaluate water molecules bound to the cartilage matrix. This study was performed to determine if there is an association between UTE-T2* relaxation time by cartilage layer and histological degeneration in knee osteoarthritis (OA).</p><p><strong>Design: </strong>Seven knees that had undergone total knee arthroplasty (TKA) were included in the study, and the lateral tibial cartilage, which had the least degeneration of the resected bones, was used as the sample. The T2* relaxation time of 4 patients with no abnormal findings on MRI was the reference relaxation time. Histological degeneration of TKA samples was assessed by the Mankin score and graded as the early OA group (≤3 points) and the advanced OA group (≥4 points). The association between T2* relaxation time and Mankin grade in each cartilage layer was compared. The effect of angiogenesis to the tidemark on T2* relaxation time was also compared.</p><p><strong>Results: </strong>T2* relaxation time of the cartilage layer was significantly longer in early OA than that in the control group. In the deep cartilage layer, the mean T2* relaxation time for angiogenesis (-) was 15.7 ms, whereas it was significantly shorter for angiogenesis (+) at 8.2 ms.</p><p><strong>Conclusions: </strong>The UTE-T2* relaxation time was associated with histological cartilage degeneration, suggesting a potential application in monitoring early cartilage degeneration.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"118-124"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11744601/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41232508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Development of a Novel Rat Knee Osteoarthritis Model Induced by Medial Meniscus Extrusion.","authors":"Daisuke Fukui, Daisuke Nishiyama, Manabu Yamanaka, Hidenobu Tamai, Naoko Nishio, Mamoru Kawakami, Hiroshi Yamada","doi":"10.1177/19476035231205680","DOIUrl":"10.1177/19476035231205680","url":null,"abstract":"<p><strong>Objective: </strong>The medial meniscus extrusion (MME) is associated with increased stress on the knee joint, which leads to cartilage degeneration. To evaluate the etiology of knee osteoarthritis, it is extremely important to create animal models of the disease that more closely resemble actual clinical conditions in terms of symptomatology, molecular biology, and histology. This study aimed to create a clinically relevant model of MME in rats.</p><p><strong>Design: </strong>Behavioral, molecular biological, and histological changes in the newly developed rat MME model were compared with those in sham and medial meniscus transection and medial collateral ligament transection (MMT) models to examine the characteristics of this model.</p><p><strong>Results: </strong>In the MME rat model, behavioral evaluation shows abnormalities in gait compared with the other 2 groups, and molecular biological evaluation of the infrapatellar synovia of rats shows that gene expression of inflammatory cytokines, matrix-degrading enzymes, and pain-related nerve growth factor was increased compared with the sham group. Furthermore, histological evaluation reveals that cartilage degeneration was the most severe in the MME group.</p><p><strong>Conclusions: </strong>The newly developed MME model reproduced the characteristic pathology of MME in clinical practice, such as severe pain, inflammation, and rapid progression of osteoarthritis. The MME model, which might more closely mimic human knee osteoarthritis (OA), could be a useful model for elucidating the pathophysiology and considering therapeutic management for knee OA.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"108-117"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11744626/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41192225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Arthroscopic Implantation of a Cell-Free Bilayer Scaffold for the Treatment of Knee Chondral Lesions: A 2-Year Prospective Study.","authors":"Rimtautas Gudas, Mantas Staškūnas, Justinas Mačiulaitis, Emilė Gudaitė, Ieva Aleknaite-Dambrauskiene","doi":"10.1177/19476035241232061","DOIUrl":"10.1177/19476035241232061","url":null,"abstract":"<p><strong>Objective: </strong>The main objective of this study is to assess the safety and clinical efficacy of a cell-free bilayer scaffold (MaioRegen Chondro+ by Fin-Ceramica) in patients affected by chondral knee lesions of different origin and localization.</p><p><strong>Design: </strong>Thirty-one patients with focal chondral lesions of the knee were arthroscopically treated with MaioRegen Chondro+. All patients were prospectively evaluated for a minimum of 2 years using the International Knee Documentation Committee (IKDC) Questionnaire and the Tegner Activity Scale. Cartilage repair was assessed based on the Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) 2.0 score at 12 months. Follow-up at 36 months was available for 25 out of 31 patients.</p><p><strong>Results: </strong>From baseline to 6-, 12-, and 24-month follow-up, IKDC score significantly improved by 19.5 ± 7.27 (95% confidence interval [CI]: 16.9-22.2, <i>P</i> < 0.001), 30.8 ± 7.63 (95% CI: 28.0-33.6, <i>P</i> < 0.001), and 36.2 ± 8.00 points (95% CI: 33.3-39.2, <i>P</i> < 0.001), respectively. Tegner scores documented a substantial clinical improvement as early as 12 months after surgery (change of -0.6 ± 0.62; 95% CI: -0.8 to -0.4, <i>P</i> < 0.001), reaching the preinjury values. There was a statistically significant increase in the MOCART scores (<i>P</i> < 0.001). Comparable results were observed regardless of preintervention demographic characteristics, lesion site or etiology, or the number of treated sites. Notably, the significant clinical benefit was maintained in a subset of patients who reached 3-year follow-up. No adverse events were reported in the entire analyzed population.</p><p><strong>Conclusion: </strong>MaioRegen Chondro+ is a safe and effective device for the treatment of knee chondral lesions, enabling a significant clinical improvement for at least 2 years.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"5-16"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11569651/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140157585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
CARTILAGEPub Date : 2025-03-01Epub Date: 2023-09-19DOI: 10.1177/19476035231200336
Xiaochuan Xiong, Hao Xiong, Jun Peng, Yingjie Liu, Yang Zong
{"title":"METTL3 Regulates the m<sup>6</sup>A Modification of NEK7 to Inhibit the Formation of Osteoarthritis.","authors":"Xiaochuan Xiong, Hao Xiong, Jun Peng, Yingjie Liu, Yang Zong","doi":"10.1177/19476035231200336","DOIUrl":"10.1177/19476035231200336","url":null,"abstract":"<p><strong>Objective: </strong>Osteoarthritis (OA) is a common degenerative joint disease. The occurrence of OA slowly destroys the soft tissue structure of the patient's joint. Severe cases could lead to disability. Current studies had shown that inhibition of chondrocytes pyroptosis could slow down the progression of OA. Our work aimed to explore the specific mechanisms and ways of regulating this process.</p><p><strong>Design: </strong>In this work, the level of N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) in clinical tissues was detected by ribonucleic acid (RNA) m<sup>6</sup>A dot blot. qRT-PCR (quantitative real-time polymerase chain reaction) was used to detect the messenger RNA (mRNA) expression level of m<sup>6</sup>A modified enzyme in clinical tissues. MTT (3-(4,5)-dimethylthiahiazo(-z-y1)-3,5-di-phenytetrazoliumromid) and flow cytometry were used to detect the effect of sh-METTL3 (methyltransferase like 3) and NIMA-related kinase 7 (NEK7) transfection on chondrocytes pyroptosis in OA. Western blot was used to detect the protein expression levels of pyroptosis-related proteins. ELISA (enzyme-linked immunosorbent assay) was used to measure the protein concentration of inflammatory cytokines. The SRAMP online database was used to predict the m<sup>6</sup>A site of NEK7. HE staining was used to assess the progression of OA in mice.</p><p><strong>Results: </strong>The level of m<sup>6</sup>A in clinical samples of OA patients was higher, and METTL3 was significantly higher expressed in clinical samples of OA patients. We provided evidence that low expression of METTL3 inhibited chondrocytes pyroptosis. In addition, Rescue experiments and <i>in vivo</i> experiments had shown that METTL3 in combination with NEK7 inhibited the progression of OA by promoting chondrocytes pyroptosis.</p><p><strong>Conclusions: </strong>METTL3 regulates m<sup>6</sup>A modification of NEK7 and inhibits OA progression.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"89-99"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11744591/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41100820","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
CARTILAGEPub Date : 2025-03-01Epub Date: 2023-10-16DOI: 10.1177/19476035231205690
Wei Xiang, Tongyi Zhang, Song Li, Yunquan Gong, Xiaoqing Luo, Jing Yuan, Yaran Wu, Xiaojing Yan, Yan Xiong, Jiqin Lian, Guangyu Zhao, Changyue Gao, Liang Kuang, Zhenhong Ni
{"title":"Cir-DNA Sequencing Revealed the Landscape of Extrachromosomal Circular DNA in Articular Cartilage and the Potential Roles in Osteoarthritis.","authors":"Wei Xiang, Tongyi Zhang, Song Li, Yunquan Gong, Xiaoqing Luo, Jing Yuan, Yaran Wu, Xiaojing Yan, Yan Xiong, Jiqin Lian, Guangyu Zhao, Changyue Gao, Liang Kuang, Zhenhong Ni","doi":"10.1177/19476035231205690","DOIUrl":"10.1177/19476035231205690","url":null,"abstract":"<p><strong>Objective: </strong>Extrachromosomal circular DNA (eccDNA) has been shown to be involved in several physiological and pathological processes including immunity, inflammation, aging, and tumor. However, the expression of eccDNA in cartilage has not been reported until now. In this study, we aimed to investigate the landscape of eccDNA in articular cartilage and analyze the potential roles in osteoarthritis (OA).</p><p><strong>Methods: </strong>The samples of articular cartilage were obtained from total knee arthroplasty (TKA) donors with OA. The mitochondrial DNA (mtDNAs) and the linear DNAs from chondrocytes of articular cartilage were removed. Then the eccDNAs were enriched for cir-DNA sequencing. After quality control evaluation, we systematically revealed the identified eccDNA data including size distribution, the size range, and sequence pattern. Moreover, we explored and discussed the potential roles of eccDNA in OA via motif analysis and Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis.</p><p><strong>Results: </strong>The chondrocytes from OA cartilage contained an abundance of eccDNAs, which was termed as OC-eccDNAs (OA cartilage-derived eccDNA). The characteristics of OC-eccDNAs were tissue-specific, including the distribution, the size range, and sequence pattern. Moreover, the functional analysis indicated that eccDNA may be involved in the homeostasis maintenance of chondrocytes and participated in the process of OA.</p><p><strong>Conclusions: </strong>Our data first showed the landscape of eccDNA in articular cartilage and preliminarily indicated the potential roles of eccDNA in OA.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"100-107"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11744593/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41232506","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
CARTILAGEPub Date : 2025-03-01Epub Date: 2023-09-12DOI: 10.1177/19476035231199442
Dong Woo Shim, Kyoung-Mi Lee, Donghyun Lee, Jun Sik Kim, Yeon Seop Jung, Sung Suk Oh, Si Wook Lee, Jin Woo Lee, Bom Soo Kim
{"title":"Osteochondral Repair with Autologous Cartilage Transplantation with or without Bone Grafting: A Short Pilot Study in Mini-Pigs.","authors":"Dong Woo Shim, Kyoung-Mi Lee, Donghyun Lee, Jun Sik Kim, Yeon Seop Jung, Sung Suk Oh, Si Wook Lee, Jin Woo Lee, Bom Soo Kim","doi":"10.1177/19476035231199442","DOIUrl":"10.1177/19476035231199442","url":null,"abstract":"<p><strong>Objective: </strong>Treatment strategies for osteochondral defects, for which particulated autologous cartilage transplantation (PACT) is an emerging treatment strategy, aim to restore the structure and function of the hyaline cartilage. Herein, we compared the efficacy of PACT with control or human transforming growth factor-β (rhTGF-β), and clarified the necessity of bone graft (BG) with PACT to treat shallow osteochondral defects in a porcine model.</p><p><strong>Design: </strong>Two skeletally mature male micropigs received 4 osteochondral defects in each knee. The 16 defects were randomized to (1) empty control, (2) PACT, (3) PACT with BG, or (4) rhTGF-β. Animals were euthanized after 2 months and histomorphometry, immunofluorescence analysis, semiquantitative evaluation (O'Driscoll score), and magnetic resonance observation of cartilage repair tissue (MOCART) score were performed.</p><p><strong>Results: </strong>Hyaline cartilages, glycosaminoglycan synthesis, and collagen type II staining were more abundant in the PACT than in the control and rhTGF-β groups. The O'Driscoll score was significantly different between groups (<i>P</i> < 0.001), with both PACT groups showing superiority (<i>P</i> = 0.002). PACT had the highest score (<i>P</i> = 0.002), with improved restoration of subchondral bone compared with PACT with BG. The MOCART score showed significant differences between groups (<i>P</i> = 0.021); MOCART and O'Driscoll scores showed high correlation (r = 0.847, <i>P</i> < 0.001).</p><p><strong>Conclusion: </strong>Treatment of osteochondral defects with PACT improved tissue quality compared with that with control or rhTGF-β in a porcine model. BG, in addition to PACT, may be unnecessary for shallow osteochondral defects. <i>Clinical Relevance.</i> BG may not be necessary while performing PACT.</p>","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"61-70"},"PeriodicalIF":2.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11744595/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10204733","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
CARTILAGEPub Date : 2025-02-21DOI: 10.1177/19476035251320747
Ju Zeng, Decui Liang, Guangyan Tang
{"title":"Grading of Cartilage Damage in Degenerative Knee Osteoarthritis Based on Quantitative Parameters of the Infrapatellar Fat Pad: A Cross-Sectional Study.","authors":"Ju Zeng, Decui Liang, Guangyan Tang","doi":"10.1177/19476035251320747","DOIUrl":"10.1177/19476035251320747","url":null,"abstract":"<p><strong>Purpose: </strong>The aim of this research was to investigate the relationship between quantitative texture parameters and degenerative cartilage damage in knee osteoarthritis (KOA) by conducting a full-volume texture analysis of infrapatellar fat pad (IFP). In addition, this study also explored if the quantitative texture parameter models outperform semi-quantitative model in cartilage damage classification tasks.</p><p><strong>Materials and methods: </strong>This retrospective study involved 202 patients who were diagnosed with KOA using imaging and clinical examinations. Texture parameters of the IFP were extracted from sagittal FSE PDWI fat-suppressed sequence images, and least absolute shrinkage and selection operator regression was used for feature selection. Spearman correlation analysis was conducted to assess the relationship between semi-quantitative parameter (Hoffa-synovitis score), quantitative parameters, and cartilage damage. Five multi-classification logistic regression models were developed to predict cartilage damage grade by using Hoffa-synovitis score, texture parameters, and clinical characteristics as independent variables. Subsequently, the performance of these models was compared.</p><p><strong>Results: </strong>Eight texture features were screened out in this study. Correlation analysis showed that Hoffa synovitis score, texture parameters, and cartilage damage grade were significantly correlated (all <i>P</i> < 0.05). The strongest correlation was found between Hoffa-synovitis score and cartilage damage, demonstrating a moderate positive relationship (<i>r</i> = 0.62). In terms of texture features, the Correlation parameter exhibited a moderate positive correlation with cartilage damage (<i>r</i> = 0.49), while other texture parameters had a slight positive correlation degree of positive or negative correlation. In the task of classifying cartilage damage, the model's macro-average area under the curve (AUC) only using the Hoffa-synovitis score was 0.73 (95% confidence interval (CI): 0.64, 0.83), while the model using only selected texture parameters achieved a macro-average AUC of 0.84 (95% CI: 0.68, 0.94). Furthermore, the model that combined texture parameters and clinical features also achieved a macro-average AUC of 0.84 (95% CI: 0.72, 0.94). By integrating the Hoffa-synovitis score, texture parameters, and clinical features, the model's macro-average AUC experienced a slight improvement to 0.85 (95% CI: 0.74, 0.93). Notably, the model combining only Hoffa-synovitis score and texture parameters had the best classification performance, with a macro-average AUC of 0.88 (95% CI: 77, 0.97). The performance of the 4 models incorporating texture parameters outperformed that of the Hoffa-synovitis score alone (all <i>P</i> < 0.05), however with no significant statistical difference observed among the 4 models (all <i>P</i> > 0.05).</p><p><strong>Conclusions: </strong>There existed a correlation between the textu","PeriodicalId":9626,"journal":{"name":"CARTILAGE","volume":" ","pages":"19476035251320747"},"PeriodicalIF":2.7,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11846089/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143466958","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}