Iliac and sacral articular cartilage of 25 human sacroiliac joints (1-
93 years) are examined by light microscopy and immunohistochemistry in
order to gain further insight into the nature and progress of degener
ative changes appearing during aging. These changes can already be see
n in younger adults as compared to cartilage degeneration known in oth
er diarthrodial joints. Structural differences between sacral and ilia
c cartilage can already be observed in the infant: the sacral auricula
r facet is covered with a hyaline articular cartilage, reaching 4 mm i
n thickness in the adult and staining intensely blue with alcian blue
at pH1. Iliac cartilage of the newborn is composed of a dense fibrilla
r network of thick collagen bundles, crossing each other at approximat
ely right angles. A faint staining with alcian blue suggests a low con
tent of acidic glycosaminoglycans. In the adult, iliac cartilage becom
es hyaline and its maximal thickness reaches 1-2 mm. Both articular fa
cets exhibit morphological changes during aging that are more pronounc
ed in the iliac cartilage and resemble osteoarthritic degeneration; th
e staining pattern of the extracellular matrix becomes inhomogenous, c
hondrocytes are arranged in clusters and the articular surface develop
s superficial irregularities and fissures. Sometimes fibrous tissue fi
lls up these defects. Nevertheless, large areas of iliac cartilage rem
ain hyaline in nature. Sacral articular cartilage often remains largel
y unaltered until old age. The sacral subchondral bone plate is usuall
y thin and shows spongiosa trabeculae inserted at right angles, sugges
ting a perpendicular load on the articular facet. Iliac subchondral sp
ongiosa shows no definite alignment and joins the thickened subchondra
l bone plate in an oblique direction. The iliac cartilage therefore se
ems to be stressed predominantly by shearing forces, arising from the
changing monopodal support of the pelvis during locomotion. The subcho
ndral bone plate on both the iliac and sacral auricular facet is penet
rated by blood vessels that come into close contact with the overlying
articular cartilage. These vessels may contribute to the high inciden
ce of rheumatoid and inflammatory diseases in the human sacroiliac joi
nt. Immunolabelling with an antibody against type Il collagen reveals
a diminished immunoreactivity in the upper half of adult sacral cartil
age and only a faint and irregular labelling in the iliac cartilage. T
ype I collagen can be detected in a superficial layer on the sacral ar
ticular surface and around chondrocyte clusters in iliac cartilage, as
in dedifferentiating chondrocytes during the development of osteoarth
ritis.