Jp. Mansell et Aj. Bailey, ABNORMAL CANCELLOUS BONE-COLLAGEN METABOLISM IN OSTEOARTHRITIS, The Journal of clinical investigation, 101(8), 1998, pp. 1596-1603
Biochemical investigations into the pathogenesis of osteoarthritis hav
e, for the last two decades, concentrated on the mechanisms involved i
n the destruction of the articular cartilage. Although bone changes ar
e known to occur, the biochemistry of the collagenous matrix within os
teoarthritic bone has received scant attention. We report that bone co
llagen metabolism is increased within osteoarthritic femoral heads, wi
th the greatest changes occurring within the subchondral zone. Collage
n synthesis and its potential to mineralize were determined by the car
boxy-terminal propeptide content and alkaline phosphatase activity, re
spectively. These data supported elevated new matrix formation. Our fi
nding of a three- to fourfold increase in TGF-beta in osteoarthritic b
one indicates that this might represent a stimulus for the increased c
ollagen synthesis observed. Of additional significance is the hypomine
ralization of deposited collagen in the subchondral zone of osteoarthr
itic femoral heads, supporting a greater proportion of osteoid in the
diseased tissue. The cross-linking of collagen was similar to that obs
erved for controls. In addition, the degradative potential of osteoart
hritic bone was considerably higher as demonstrated by increased matri
x metalloproteinase 2 activity, and again the greater activity was ass
ociated with the subchondral bone tissue. The polarization exhibited i
n the metabolism of bone collagen from osteoarthritic hips might exace
rbate the processes involved in joint deterioration by altering joint
morphology. This in turn may alter the distribution of mechanical forc
es to the various tissues, to which bone is a sensitive responder. Bon
e collagen metabolism is clearly an important factor in the pathogenes
is of osteoarthritis and certainly warrants further biochemical study.