Hk. Gahunia et al., OSTEOARTHRITIS IN RHESUS MACAQUE KNEE-JOINT - QUANTITATIVE MAGNETIC-RESONANCE-IMAGING TISSUE CHARACTERIZATION OF ARTICULAR-CARTILAGE, Journal of rheumatology, 22(9), 1995, pp. 1747-1756
Objective. To assess cartilage matrix quality variation by anatomical
location and extent of osteoarthritis (OA) using quantitative magnetic
resonance imaging (MRI) and to compare the anatomic MR morphologic fe
atures with corresponding histological findings. Methods. We studied 1
8 fully encapsulated right knee joints from a population of rhesus mon
keys with a high incidence of degenerative arthritis resembling human
OA. Relaxation times (T1 and T2), spin density, and cartilage thicknes
s were determined along 8 contiguous anteroposterior segments of artic
ular cartilage. Histological slides, prepared in the same plane as the
MR image, were assessed for OA severity. Using a modification of Mank
in's OA classification, each quadrant was grouped into normal (0), mil
d (1), moderate (2), or severe OA (3). Histopathological scores served
as the standard and corresponding MR quadrants were classified accord
ingly. Results. Cumulative results revealed a significant decrease in
T1 relaxation time (p = 0.04) and an increase in T2 relaxation time (p
= 0.03) in the mild and severe OA groups, respectively. Statistically
significant changes in spin density and cartilage thickness measureme
nts were not observed. MR signal intensity abnormalities in selected r
egions of interest were demarcated and studied histologically. Regions
with histological proliferating chondrocytes or fibrillated cartilage
showed bright signal intensity on MR images (TR = 3000 ms; TE = 10 ms
) and corresponded with elevated T1 and T2 values. Histological region
s of collagen condensation showed low signal intensity on MR images (T
R = 3000 ms; TE = 10 ms) and corresponded with decreased T1 and T2 rel
axation times. Conclusion. Topological quantitative MRI relaxation tim
e assessment demonstrates increasing cartilage matrix quality variatio
n with OA progression.