MICROSCOPIC MEASUREMENT OF SYNOVIAL-MEMBRANE INFLAMMATION IN RHEUMATOID-ARTHRITIS - PROPOSALS FOR THE EVALUATION OF TISSUE SAMPLES BY QUANTITATIVE-ANALYSIS
B. Bresnihan et al., MICROSCOPIC MEASUREMENT OF SYNOVIAL-MEMBRANE INFLAMMATION IN RHEUMATOID-ARTHRITIS - PROPOSALS FOR THE EVALUATION OF TISSUE SAMPLES BY QUANTITATIVE-ANALYSIS, British journal of rheumatology, 37(6), 1998, pp. 636-642
Previous studies have used various techniques for microscopic analysis
of rheumatoid synovium, ranging from rapid analysis of limited areas
of tissue to detailed quantification of extensive areas. The sensitivi
ty and reproducibility of these methods have not been tested. This stu
dy sought to determine the minimum area of rheumatoid synovium needed
to allow accurate microscopic analysis of synovial inflammation. Multi
ple synovial tissue samples were obtained from patients with rheumatoi
d arthritis at knee arthroplasty (n = 10), knee arthroscopy (n = 10) a
nd by blind needle biopsy (n = 23). Lining layer thickness, sublining
T-cell infiltration and vascularity were measured in all high-power fi
elds (hpf) throughout every sample obtained from each patient. These c
omplete measured results were compared with estimated results from lim
ited numbers of hpf from each patient. It was observed that lining lay
er thickness estimated from as few as five readings from 3 samples/pat
ient correlated significantly with the measured results obtained from
as many as 85 readings/patient [Tau (T) = 0.70-0.94 for the three grou
ps, all P < 0.005). Estimated measures of T-cell infiltration and vasc
ularity derived from only 17 randomly selected hpf from 3 samples/pati
ent (equivalent to 1 mm(2)) correlated significantly with the measured
results obtained from up to 150 hpf/patient (T = 0.65-0.94, all P les
s than or equal to 0.002). Quantitative analysis of inflammation in sy
novial tissue samples is both accurate and practical when restricted t
o an evaluation of a limited number of microscopic fields. It is propo
sed that lining layer thickness may be confidently quantified from fiv
e randomly selected readings from three tissue samples, and that subli
ning T-cell infiltration and vascularity may be quantified from 17 ran
domly selected hpf from the same samples.