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Bone Microdamage in Acute Knee Injury
Logeswaran Selvarajah1, Annie M Curtis2, Oran D Kennedy3
1Department of Anatomy, Royal College of Surgeons in Ireland, 123 St Stephens Green, Dublin 2, Ireland. logesselva@rcsi.ie.
Purpose Of Review:
This review summarizes what is known about how bone tissue responds to microdamage, and how this applies to the subchondral region. This has significant relevance to acute joint injury, and is related to the occurrence of bone marrow lesions (BMLs) which are seen by MRI in 80% of acute knee joint injuries. Here, we review what is known about these phenomena (microcracks and BMLs) in the literature and discuss potential mechanisms by which they may be linked.
Recent Findings:
The recent findings in this field have shown that microcracks in bone initiate targeted remodeling via RANKL expression in osteocytes. Other work has shown that subchondral microcracks co-localize with BMLs as viewed by MRI. Finally, BMLs are associated with pain and structural joint degeneration. This paper demonstrates that subchondral microcracks likely occur during acute joint injury, and are closely linked to BML that are seem by clinical MRI and thus are potentially involved in the subsequent joint degeneration that occurs after injury.
Insights
Bone microdamage, particularly in the subchondral bone, is closely linked to bone marrow lesions (BMLs) after acute joint injury. This connection may explain subsequent joint degeneration and pain.
Area of Science:
- Orthopedics
- Bone Biology
- Radiology
Background:
- Bone tissue responds to microdamage through targeted remodeling.
- Subchondral bone is susceptible to microdamage, especially after acute joint injury.
- Bone marrow lesions (BMLs) are frequently observed via MRI following acute knee injuries.
Purpose of the Study:
- To review the current understanding of bone tissue's response to microdamage.
- To explore the relationship between subchondral microdamage and BMLs.
- To discuss the implications for acute joint injury and subsequent joint degeneration.
Main Methods:
- Literature review of studies on bone microdamage and BMLs.
- Analysis of MRI findings in acute joint injuries.
- Discussion of potential pathomechanisms linking microcracks and BMLs.
Main Results:
- Microcracks in bone initiate osteocyte-mediated remodeling via RANKL expression.
- Subchondral microcracks observed via MRI correlate spatially with BMLs.
- BMLs are associated with joint pain and progressive structural joint degeneration.
Conclusions:
- Subchondral microcracks are likely initiated during acute joint injury.
- These microcracks are closely associated with clinically observed BMLs.
- The link between microcracks and BMLs suggests a role in post-injury joint degeneration.
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