Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 May 9;58(7):894-904.
doi: 10.1007/s43465-024-01168-6. eCollection 2024 Jul.

Bone Marrow Aspirate Concentrate for Treatment of Primary Knee Osteoarthritis: A Prospective, Single-Center, Non-randomized Study with 2-Year Follow-Up

Affiliations

Bone Marrow Aspirate Concentrate for Treatment of Primary Knee Osteoarthritis: A Prospective, Single-Center, Non-randomized Study with 2-Year Follow-Up

Madhan Jeyaraman et al. Indian J Orthop. .

Abstract

Introduction: Knee osteoarthritis (OA) is a widespread, disabling condition with no intervention to fully restore cartilage or halt progression. Bone marrow aspirate concentrate (BMAC), an autologous product from bone marrow aspiration, has shown promise as a regenerative therapy due to its cell composition and chondrogenic effects. Our study aims to assess the functional outcomes, including pain, function, satisfaction, and complications post-BMAC injection in knee OA patients.

Materials and methods: In this prospective, single-center study, 63 patients with grade II-III knee OA (Kellgren-Lawrence (K-L) scale) unresponsive to conservative management underwent BMAC injection. The procedure involved bone marrow aspiration from the anterior iliac crest, processing to obtain a concentrate, followed by intra-articular injection. Patients were followed for 24 months, assessing outcomes using the Visual Analog Scale (VAS), International Knee Documentation Committee (IKDC) score, and MOCART 2.0 score.

Results: The cohort, with a slight female predominance and predominantly aged 41-50 years, majorly comprised K-L grade III OA patients. BMAC treatment resulted in significant improvements in VAS pain scores, IKDC functional scores, and MOCART 2.0 scores over the 24-month follow-up.

Conclusion: BMAC injection provides significant improvement in both pain and functional outcomes at mid-term follow-up in patients with mild-to-moderate OA of the knee. Further high-quality, adequately powered, multi-center, prospective, double-blinded, randomized controlled trials with longer follow-up are necessary to justify the routine clinical use of BMAC for treatment of patients suffering with knee OA.

Keywords: BMAC; Bone marrow aspirate; Bone marrow aspirate concentrate; Knee; Knee osteoarthritis; Regenerative medicine.

PubMed Disclaimer

Conflict of interest statement

Conflicts of InterestThe authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Aspiration of bone marrow from the right iliac crest
Fig. 2
Fig. 2
Intra-articular injection of BMAC via antero-superolateral portal into left knee joint
Fig. 3
Fig. 3
Schematic representation of BMAC isolation (created with Biorender.com)
Fig. 4
Fig. 4
VAS score at various follow-up time points compared to the baseline. *Represents p < 0.05 compared to baseline
Fig. 5
Fig. 5
IKDC score at various follow-up time points compared to the baseline. *Represents p < 0.05 compared to baseline
Fig. 6
Fig. 6
A Pre-procedural radiograph of bilateral knees (AP view on standing position) showing decreased medial joint line in bilateral knees suggestive of KL grade II knee OA and B 2-year follow-up radiograph of bilateral knees (AP view on standing position) showing the maintenance of medial joint line in bilateral knees indicating response to BMAC therapy
Fig. 7
Fig. 7
A Pre-procedural T2W MRI (coronal section) showing hyperintensity with thinned out cartilage along the medial femoral condyle suggestive of OA knee and B 2-year follow-up T2W MRI (coronal image) showing increased cartilaginous thickness with a relatively maintained cartilaginous signal indicating response to BMAC therapy

References

    1. He Y, Li Z, Alexander PG, Ocasio-Nieves BD, Yocum L, Lin H, et al. Pathogenesis of osteoarthritis: Risk factors, regulatory pathways in chondrocytes, and experimental models. Biology. 2020;9(8):194. doi: 10.3390/biology9080194. - DOI - PMC - PubMed
    1. Yunus MHM, Nordin A, Kamal H. Pathophysiological perspective of osteoarthritis. Medicina (Kaunas, Lithuania) 2020;56(11):614. doi: 10.3390/medicina56110614. - DOI - PMC - PubMed
    1. Tong L, Yu H, Huang X, Shen J, Xiao G, Chen L, et al. Current understanding of osteoarthritis pathogenesis and relevant new approaches. Bone Research. 2022;10(1):1–17. doi: 10.1038/s41413-022-00226-9. - DOI - PMC - PubMed
    1. Zhang L, Hu J, Athanasiou KA. The role of tissue engineering in articular cartilage repair and regeneration. Critical Reviews in Biomedical Engineering. 2009;37(1–2):1–57. doi: 10.1615/CritRevBiomedEng.v37.i1-2.10. - DOI - PMC - PubMed
    1. Fox AJS, Bedi A, Rodeo SA. The basic science of articular cartilage. Sports Health. 2009;1(6):461–468. doi: 10.1177/1941738109350438. - DOI - PMC - PubMed

LinkOut - more resources