The Journal of Bone and Joint Surgery (American). 2006;88:2201-2209.
doi:10.2106/JBJS.E.00812
© 2006 The Journal of Bone and Joint Surgery, Inc.
Effect of Early Full Weight-Bearing After Joint Injury on Inflammation and Cartilage Degradation
D.M. Green, MD1,
P.C. Noble, PhD2,
J.R. Bocell, Jr., MD2,
J.S. Ahuero, MD2,
B.A. Poteet, DVM3 and
H.H. Birdsall, MD, PhD1
1 Research Office, MS 151, Michael E. DeBakey Veterans Affairs Medical Center,
2002 Holcombe Boulevard, Houston, TX 77030. E-mail address for D.M. Green:
dgreen{at}bcm.tmc.edu
2 Department of Orthopedic Surgery, Baylor College of Medicine, Houston, TX
77030
3 Gulf Coast Veterinary Specialists, 1111 West Loop South, Houston, TX
77027
Investigation performed at Baylor College of Medicine and Michael E.
DeBakey Veterans Affairs Medical Center, Houston, Texas
In support of their research for or preparation of this manuscript, one or
more of the authors received grants or outside funding from the Institute of
Orthopaedic Research and Education and the Baylor Orthopedic Research Fund.
None of the authors received payments or other benefits or a commitment or
agreement to provide such benefits from a commercial entity. No commercial
entity paid or directed, or agreed to pay or direct, any benefits to any
research fund, foundation, educational institution, or other charitable or
nonprofit organization with which the authors are affiliated or associated.
The Department of Veterans Affairs, Houston, Texas, provided laboratory space
for the work.
Background: Early full weight-bearing after an acute osteochondral
injury avoids problems associated with immobility but may also be harmful by
amplifying the inflammatory response. To investigate these effects, we
developed an in vivo model of subchondral trauma.
Methods: After an impact injury to the femoral condyle, fourteen
dogs were randomized to immediate full weight-bearing or to four weeks of
minimal weight-bearing before full weight-bearing. Synovial fluid was sampled
by aspiration at one, two, four, eight, twelve, sixteen, twenty, and
twenty-four weeks. Neutrophils, monocytes, and lymphocytes were enumerated,
and the concentrations of tumor necrosis factor-alpha, interleukin-10, nitric
oxide, matrix metalloproteinases, and glycosaminoglycans were measured.
Results: Compared with the findings for uninjured joints, the
synovial fluid from the impacted joints of full-weight-bearing dogs had
significantly higher peak concentrations of neutrophils (p = 0.0006 at one
week), mononuclear leukocytes (p = 0.001 at four weeks), tumor necrosis
factor-alpha (p = 0.001 at one week), nitric oxide (p = 0.001 at one week),
matrix metalloproteinases (p = 0.008 at one week), and glycosaminoglycans (p =
0.002 at four weeks and p = 0.001 at six months). The size of the bone bruise
correlated with the peak concentrations of tumor necrosis factor-alpha
(r2 = 0.89, p = 0.007; Spearman rank test), matrix
metalloproteinases (r2 = 0.96, p = 0.0004), and glycosaminoglycans
(r2 = 0.96, p = 0.0004). However, restriction to minimal
weight-bearing for four weeks after the injury led to a significant reduction
in the synovial fluid concentrations of neutrophils (p = 0.007 at one week and
p = 0.01 at two weeks), tumor necrosis factor-alpha (p = 0.0006 to 0.02 during
the first four weeks), nitric oxide (p = 0.001 to 0.04 during the first four
weeks), and matrix metalloproteinases (p = 0.007 to 0.01 from the second week
to the eighth week). In contrast, interleukin-10 concentrations were
significantly higher (p = 0.002 at one week) and glycosaminoglycan levels
remained at normal levels in animals that were restricted from immediate full
weight-bearing after the injury.
Conclusions: The magnitude of the inflammatory response is
proportional to the size of the bone bruise. Restriction to minimal
weight-bearing for four weeks reduces the magnitude of the inflammatory
response and the cartilage degradation following articular cartilage impact
injury.
Clinical Relevance: Strategies to minimize mechanical stress during
the early postinjury period may help to preserve cartilage integrity and
forestall the development of osteoarthritis.

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