J. Kumagai et al., THE COLLAGEN TYPES IN THE ATTACHMENT ZONE OF ROTATOR CUFF TENDONS IN THE ELDERLY - AN IMMUNOHISTOCHEMICAL STUDY, Journal of rheumatology, 21(11), 1994, pp. 2096-2100
Objective. The attachment zone of the rotator cuff tendons in the elde
rly was studied immunohistochemically in order to determine how degene
rative changes affected the pattern of collagen fiber distribution. Me
thods. Twenty-seven cuffs with their bony insertion were obtained from
22 postmortem cases of both sexes ranging in age from 52 to 90 years
and without a history of shoulder ailments. In addition, 3 cuff specim
ens from cadavers in the 3rd and 4th decades were examined for compari
son. Sections of formalin fixed tissues were stained by peroxidase ant
iperoxidase (PAP) technique using monoclonal antibodies against types
I, II and III collagen. Results. Degenerative changes affecting the fi
brocartilage primarily were characterized by calcification, fibrovascu
lar proliferation and microtears. In addition, they were found in all
the cuff tendons of elderly individuals but not in those from younger
subjects. Immunohistochemically, the attachment zone in areas without
degenerative lesions showed collagen type I labelling strongly in bone
but only moderately in the fibrocartilage. The predominant labelling
in the fibrocartilage was for collagen type II, and collagen type III
labelled principally in perichondrocytic areas. The tidemark showed in
consistent labelling for any of the collagen types. In the presence of
degenerative lesions, the disposition of fiber types was interrupted
by calcification and microtears. Collagen type II composition of the f
ibrocartilage was markedly altered by the presence of fibrovascular ti
ssue which labelled only for collagen type III. Conclusion. We conclud
e that severe degenerative changes in the cuff tendons of elderly indi
viduals, alter the collagen characteristic of the rotator cuff and tha
t the changes could be associated with impairment of biomechanical pro
perties of the attachment zone, and may give rise to the clinical synd
rome of enthesopathy.