G. Spencergreen et al., TEST-PERFORMANCE IN SYSTEMIC-SCLEROSIS - ANTICENTROMERE AND ANTI-SCL-70 ANTIBODIES, The American journal of medicine, 103(3), 1997, pp. 242-248
PURPOSE: TO determine the sensitivity and specificity of anti-centrome
re (ACA) and anti-Scl-70 antibodies in systemic sclerosis (SSc). METHO
DS: Four-hundred ninety-seven English language articles published from
1966 to 1994 were identified by structured MEDLINE search. Articles i
n which either ACA or anti-Scl-70 antibodies were measured in both SSc
patients and a non-SSc control group were reviewed and rated using a
previously published diagnostic testing scale. Reported sensitivity an
d specificity from each study was converted into a 2 x 2 table, and co
mbined across studies to calculate summary rates for each antibody. Au
thor's clinical classification criteria for SSc served as the gold sta
ndard for disease diagnosis. RESULTS: In 30 articles that fulfilled in
clusion criteria, ACA were found in 441 of 1,379 SSc patients (sensiti
vity 32%, range 17% to 56%). This increased to 57% (332 of 585) in pat
ients with the limited cutaneous, or CREST, subset of SSc (lcSSc). Ant
i-Scl-70 antibodies were found in 366 of 1,074 SSc patients (sensitivi
ty 34%, range 3% to 75%), and this increased slightly to 40% in patien
ts with the diffuse cutaneous form of SSc (dcSSc). Both antibodies wer
e measured in 670 patients, and either test was positive in 58% (range
29% to 86%), but in only 3 patients were both antibodies present. The
specificity of each antibody was high, but varied by control group. A
CA were present in 5% and anti-Scl-70 antibodies were present in 2% of
patients with other connective tissue diseases, but fewer than 1% of
disease free controls had either antibody present. CONCLUSIONS: As ind
ividual diagnostic tests in SSc, both ACA and anti-Scl-70 antibodies a
re highly specific. Each performs somewhat better as discriminators of
clinical subsets for patients in whom a diagnosis of SSc has already
been established. Clinicians can rely on a positive test result as bei
ng specific in the detection of disease, but 40% of SSc patients are l
ikely to have neither antibody present, and a negative result does not
exclude the diagnosis. Measurement of these antibodies should be cons
idered secondary to the clinical features when making a diagnosis of S
Sc. (C) 1997 by Excerpta Medica, Inc.