Transplantation of autologous bone marrow-derived mesenchymal stem cells under arthroscopic surgery with microfracture versus microfracture alone for articular cartilage lesions in the knee: A multicenter prospective randomized control clinical trial
To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone. Eleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They...
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Published in | Regenerative therapy Vol. 11; pp. 106 - 113 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.12.2019
Japanese Society for Regenerative Medicine Elsevier |
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Abstract | To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone.
Eleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They were randomized to receive BMSCs with MFX (cell-T group, n=7) or MFX alone (control group, n=4). Clinical results were evaluated using International Knee Documentation committee (IKDC) knee evaluation questionnaires and the Knee Injury and Osteoarthritis Outcome Score (KOOS) before and 48 weeks after surgery. Quantitative and qualitative assessments of repair tissue were carried out at 48 weeks by T2 mapping of magnetic resonance images (MRIs) and the magnetic resonance observation of cartilage repair tissue (MOCART) scoring system with follow-up MRI.
No significant differences between preoperative and postoperative IKDC and KOOS were observed in the cell-T or control group. However, forty-eight weeks after surgery, the cell-T group showed a trend for a greater KOOS QOL score compared with the control group (79.4 vs. 39.1, respectively; P=0.07). The T2 value did not differ significantly between the two groups, but the mean MOCART score was significantly higher in the cell-T group than in the control group (P=0.02).
Compared with MFX alone, BMSC transplantation with MFX resulted in better postoperative healing of the cartilage and subchondral bone as determined by the MOCART score. Clinically, BMSC transplantation with MFX gave a higher KOOS QOL score after 48 weeks.
•This is the first prospective randomized clinical trial between BMSCs with MFX and MFX alone.•BMSCs with MFX showed a trend for a greater KOOS QOL score compared with MFX alone.•BMSCs with MFX resulted in better healing of the cartilage by the MOCART score. |
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AbstractList | To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone.
Eleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They were randomized to receive BMSCs with MFX (cell-T group, n=7) or MFX alone (control group, n=4). Clinical results were evaluated using International Knee Documentation committee (IKDC) knee evaluation questionnaires and the Knee Injury and Osteoarthritis Outcome Score (KOOS) before and 48 weeks after surgery. Quantitative and qualitative assessments of repair tissue were carried out at 48 weeks by T2 mapping of magnetic resonance images (MRIs) and the magnetic resonance observation of cartilage repair tissue (MOCART) scoring system with follow-up MRI.
No significant differences between preoperative and postoperative IKDC and KOOS were observed in the cell-T or control group. However, forty-eight weeks after surgery, the cell-T group showed a trend for a greater KOOS QOL score compared with the control group (79.4 vs. 39.1, respectively; P=0.07). The T2 value did not differ significantly between the two groups, but the mean MOCART score was significantly higher in the cell-T group than in the control group (P=0.02).
Compared with MFX alone, BMSC transplantation with MFX resulted in better postoperative healing of the cartilage and subchondral bone as determined by the MOCART score. Clinically, BMSC transplantation with MFX gave a higher KOOS QOL score after 48 weeks.
•This is the first prospective randomized clinical trial between BMSCs with MFX and MFX alone.•BMSCs with MFX showed a trend for a greater KOOS QOL score compared with MFX alone.•BMSCs with MFX resulted in better healing of the cartilage by the MOCART score. Introduction: To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone. Methods: Eleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They were randomized to receive BMSCs with MFX (cell-T group, n=7) or MFX alone (control group, n=4). Clinical results were evaluated using International Knee Documentation committee (IKDC) knee evaluation questionnaires and the Knee Injury and Osteoarthritis Outcome Score (KOOS) before and 48 weeks after surgery. Quantitative and qualitative assessments of repair tissue were carried out at 48 weeks by T2 mapping of magnetic resonance images (MRIs) and the magnetic resonance observation of cartilage repair tissue (MOCART) scoring system with follow-up MRI. Results: No significant differences between preoperative and postoperative IKDC and KOOS were observed in the cell-T or control group. However, forty-eight weeks after surgery, the cell-T group showed a trend for a greater KOOS QOL score compared with the control group (79.4 vs. 39.1, respectively; P=0.07). The T2 value did not differ significantly between the two groups, but the mean MOCART score was significantly higher in the cell-T group than in the control group (P=0.02). Conclusions: Compared with MFX alone, BMSC transplantation with MFX resulted in better postoperative healing of the cartilage and subchondral bone as determined by the MOCART score. Clinically, BMSC transplantation with MFX gave a higher KOOS QOL score after 48 weeks. Keywords: Bone marrow-derived mesenchymal stem cells, Microfracture, Prospective randomized control clinical trial To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone. Eleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They were randomized to receive BMSCs with MFX (cell-T group, n=7) or MFX alone (control group, n=4). Clinical results were evaluated using International Knee Documentation committee (IKDC) knee evaluation questionnaires and the Knee Injury and Osteoarthritis Outcome Score (KOOS) before and 48 weeks after surgery. Quantitative and qualitative assessments of repair tissue were carried out at 48 weeks by T2 mapping of magnetic resonance images (MRIs) and the magnetic resonance observation of cartilage repair tissue (MOCART) scoring system with follow-up MRI. No significant differences between preoperative and postoperative IKDC and KOOS were observed in the cell-T or control group. However, forty-eight weeks after surgery, the cell-T group showed a trend for a greater KOOS QOL score compared with the control group (79.4 vs. 39.1, respectively; P=0.07). The T2 value did not differ significantly between the two groups, but the mean MOCART score was significantly higher in the cell-T group than in the control group (P=0.02). Compared with MFX alone, BMSC transplantation with MFX resulted in better postoperative healing of the cartilage and subchondral bone as determined by the MOCART score. Clinically, BMSC transplantation with MFX gave a higher KOOS QOL score after 48 weeks. To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone.INTRODUCTIONTo investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX) compared with microfracture alone.Eleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They were randomized to receive BMSCs with MFX (cell-T group, n=7) or MFX alone (control group, n=4). Clinical results were evaluated using International Knee Documentation committee (IKDC) knee evaluation questionnaires and the Knee Injury and Osteoarthritis Outcome Score (KOOS) before and 48 weeks after surgery. Quantitative and qualitative assessments of repair tissue were carried out at 48 weeks by T2 mapping of magnetic resonance images (MRIs) and the magnetic resonance observation of cartilage repair tissue (MOCART) scoring system with follow-up MRI.METHODSEleven patients with a symptomatic articular cartilage defect of the knee were included in the study. They were randomized to receive BMSCs with MFX (cell-T group, n=7) or MFX alone (control group, n=4). Clinical results were evaluated using International Knee Documentation committee (IKDC) knee evaluation questionnaires and the Knee Injury and Osteoarthritis Outcome Score (KOOS) before and 48 weeks after surgery. Quantitative and qualitative assessments of repair tissue were carried out at 48 weeks by T2 mapping of magnetic resonance images (MRIs) and the magnetic resonance observation of cartilage repair tissue (MOCART) scoring system with follow-up MRI.No significant differences between preoperative and postoperative IKDC and KOOS were observed in the cell-T or control group. However, forty-eight weeks after surgery, the cell-T group showed a trend for a greater KOOS QOL score compared with the control group (79.4 vs. 39.1, respectively; P=0.07). The T2 value did not differ significantly between the two groups, but the mean MOCART score was significantly higher in the cell-T group than in the control group (P=0.02).RESULTSNo significant differences between preoperative and postoperative IKDC and KOOS were observed in the cell-T or control group. However, forty-eight weeks after surgery, the cell-T group showed a trend for a greater KOOS QOL score compared with the control group (79.4 vs. 39.1, respectively; P=0.07). The T2 value did not differ significantly between the two groups, but the mean MOCART score was significantly higher in the cell-T group than in the control group (P=0.02).Compared with MFX alone, BMSC transplantation with MFX resulted in better postoperative healing of the cartilage and subchondral bone as determined by the MOCART score. Clinically, BMSC transplantation with MFX gave a higher KOOS QOL score after 48 weeks.CONCLUSIONSCompared with MFX alone, BMSC transplantation with MFX resulted in better postoperative healing of the cartilage and subchondral bone as determined by the MOCART score. Clinically, BMSC transplantation with MFX gave a higher KOOS QOL score after 48 weeks. • This is the first prospective randomized clinical trial between BMSCs with MFX and MFX alone. • BMSCs with MFX showed a trend for a greater KOOS QOL score compared with MFX alone. • BMSCs with MFX resulted in better healing of the cartilage by the MOCART score. |
Author | Akagi, Masao Kashiwa, Kaori Mera, Hisashi Inagaki, Yusuke Wakitani, Shigeyuki Kamei, Naosuke Adachi, Nobuo Hashimoto, Yusuke Takahashi, Shinji Asada, Shigeki Ishikawa, Masakazu Nakamura, Hiroaki Hosokawa, Yoshiya Nishida, Yohei Myoui, Akira Ochi, Mitsuo Yoshiya, Shinichi Fukuda, Kanji Tanaka, Yasuhito Uematsu, Kota |
AuthorAffiliation | h Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences. Hiroshima University, Hiroshima, Japan d Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan g Medical Center for Translational Research, Osaka University Hospital, Osaka, Japan e Department of Orthopaedic Surgery, Kindai University Faculty Medicine, Osaka, Japan f Institute of Advanced Clinical Medicine, Division of Cell Biology for Regenerative Medicine, Faculty of Medicine, Kindai University, Osaka, Japan b Department of Orthopaedic Surgery, Uonuma Kikan Hospital, Minamiuonuma, Japan i Department of Orthopaedic Surgery, Koryokai Hospital, Osaka, Japan c Department of Orthopaedic Surgery, Hyogo College of Medicine, Hyogo, Japan a Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan |
AuthorAffiliation_xml | – name: b Department of Orthopaedic Surgery, Uonuma Kikan Hospital, Minamiuonuma, Japan – name: c Department of Orthopaedic Surgery, Hyogo College of Medicine, Hyogo, Japan – name: h Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences. Hiroshima University, Hiroshima, Japan – name: a Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan – name: g Medical Center for Translational Research, Osaka University Hospital, Osaka, Japan – name: e Department of Orthopaedic Surgery, Kindai University Faculty Medicine, Osaka, Japan – name: d Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan – name: i Department of Orthopaedic Surgery, Koryokai Hospital, Osaka, Japan – name: f Institute of Advanced Clinical Medicine, Division of Cell Biology for Regenerative Medicine, Faculty of Medicine, Kindai University, Osaka, Japan |
Author_xml | – sequence: 1 givenname: Yusuke surname: Hashimoto fullname: Hashimoto, Yusuke email: hussy@med.osaka-cu.ac.jp organization: Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan – sequence: 2 givenname: Yohei surname: Nishida fullname: Nishida, Yohei email: haru_the_49ers@yahoo.co.jp organization: Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan – sequence: 3 givenname: Shinji surname: Takahashi fullname: Takahashi, Shinji email: a99m042@yahoo.co.jp organization: Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan – sequence: 4 givenname: Hiroaki surname: Nakamura fullname: Nakamura, Hiroaki email: hnakamura@med.osaka-cu.ac.jp organization: Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan – sequence: 5 givenname: Hisashi surname: Mera fullname: Mera, Hisashi email: hisme0214@gmail.com organization: Department of Orthopaedic Surgery, Uonuma Kikan Hospital, Minamiuonuma, Japan – sequence: 6 givenname: Kaori surname: Kashiwa fullname: Kashiwa, Kaori email: kaok48@yahoo.co.jp organization: Department of Orthopaedic Surgery, Hyogo College of Medicine, Hyogo, Japan – sequence: 7 givenname: Shinichi surname: Yoshiya fullname: Yoshiya, Shinichi email: yoshiya0307@gmail.com organization: Department of Orthopaedic Surgery, Hyogo College of Medicine, Hyogo, Japan – sequence: 8 givenname: Yusuke surname: Inagaki fullname: Inagaki, Yusuke email: yinagaki@naramed-u.ac.jp organization: Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan – sequence: 9 givenname: Kota surname: Uematsu fullname: Uematsu, Kota email: k-uematsu@nara-jadecom.jp organization: Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan – sequence: 10 givenname: Yasuhito surname: Tanaka fullname: Tanaka, Yasuhito email: yatanaka@naramed-u.ac.jp organization: Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan – sequence: 11 givenname: Shigeki surname: Asada fullname: Asada, Shigeki email: asada@med.kindai.ac.jp organization: Department of Orthopaedic Surgery, Kindai University Faculty Medicine, Osaka, Japan – sequence: 12 givenname: Masao surname: Akagi fullname: Akagi, Masao email: makagi@med.kindai.ac.jp organization: Department of Orthopaedic Surgery, Kindai University Faculty Medicine, Osaka, Japan – sequence: 13 givenname: Kanji surname: Fukuda fullname: Fukuda, Kanji email: fukuda@med.kindai.ac.jp organization: Institute of Advanced Clinical Medicine, Division of Cell Biology for Regenerative Medicine, Faculty of Medicine, Kindai University, Osaka, Japan – sequence: 14 givenname: Yoshiya surname: Hosokawa fullname: Hosokawa, Yoshiya email: yoshiyahosokawa@endmet.med.osaka-u.ac.jp organization: Medical Center for Translational Research, Osaka University Hospital, Osaka, Japan – sequence: 15 givenname: Akira surname: Myoui fullname: Myoui, Akira email: myoi@hp-mctr.med.osaka-u.ac.jp organization: Medical Center for Translational Research, Osaka University Hospital, Osaka, Japan – sequence: 16 givenname: Naosuke surname: Kamei fullname: Kamei, Naosuke email: nahkamei@hiroshima-u.ac.jp organization: Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences. Hiroshima University, Hiroshima, Japan – sequence: 17 givenname: Masakazu surname: Ishikawa fullname: Ishikawa, Masakazu email: mishikawa@hiroshima-u.ac.jp organization: Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences. Hiroshima University, Hiroshima, Japan – sequence: 18 givenname: Nobuo surname: Adachi fullname: Adachi, Nobuo email: nadachi@hiroshima-u.ac.jp organization: Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences. Hiroshima University, Hiroshima, Japan – sequence: 19 givenname: Mitsuo surname: Ochi fullname: Ochi, Mitsuo email: ochim@hiroshima-u.ac.jp organization: Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences. Hiroshima University, Hiroshima, Japan – sequence: 20 givenname: Shigeyuki surname: Wakitani fullname: Wakitani, Shigeyuki email: swakitani44@gmail.com organization: Department of Orthopaedic Surgery, Koryokai Hospital, Osaka, Japan |
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Keywords | KL RCT Microfracture IKDC Prospective randomized control clinical trial KOOS MRIs QOL GFP CPC HA Bone marrow-derived mesenchymal stem cells BMSCs MFX MOCART GFP, green fluorescent protein MOCART, magnetic resonance observation of cartilage repair tissue CPC, cell processing centers KL, Kellgren–Lawrence KOOS, Knee Injury and Osteoarthritis Outcome Score MRIs, magnetic resonance images HA, hyaluronic acid BMSCs, bone marrow-derived mesenchymal stem cells RCT, randomized controlled trial QOL, quality of life MFX, microfracture IKDC, International Knee Documentation committee |
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Snippet | To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with microfracture (MFX)... • This is the first prospective randomized clinical trial between BMSCs with MFX and MFX alone. • BMSCs with MFX showed a trend for a greater KOOS QOL score... Introduction: To investigate the efficacy of the transplantation of autologous bone marrow-derived mesenchymal stem cells (BMSCs) under arthroscopy with... |
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SubjectTerms | Bone marrow-derived mesenchymal stem cells Microfracture Original Prospective randomized control clinical trial |
Title | Transplantation of autologous bone marrow-derived mesenchymal stem cells under arthroscopic surgery with microfracture versus microfracture alone for articular cartilage lesions in the knee: A multicenter prospective randomized control clinical trial |
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