Optimization and diagnostic performance of a single multiparameter lineblot in the serological workup of systemic sclerosis

被引:36
作者
Bonroy, C. [1 ]
Van Praet, J. [2 ]
Smith, V. [2 ]
Van Steendam, K. [3 ]
Mimori, T. [4 ]
Deschepper, E. [5 ]
Deforce, D. [3 ]
Devreese, K. [1 ]
De Keyser, F. [2 ]
机构
[1] Ghent Univ Hosp 2P8, Lab Clin Biol, Dept Clin Chem Microbiol & Immunol, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp 0K12, Dept Rheumatol, B-9000 Ghent, Belgium
[3] Univ Ghent, Lab Pharmaceut Biotechnol, B-9000 Ghent, Belgium
[4] Kyoto Univ, Grad Sch Med, Dept Rheumatol & Clin Immunol, Sakyo Ku, Kyoto 6068507, Japan
[5] Univ Ghent, Biostat Unit, B-9000 Ghent, Belgium
关键词
Anti-extractable nuclear antigen antibodies; Systemic sclerosis; Anti-RNA-polymerase-III antibodies; Anti-PM/Scl antibodies; Lineblot; Diagnostic accuracy; RNA-POLYMERASE-III; LINKED-IMMUNOSORBENT-ASSAY; CONNECTIVE-TISSUE DISORDERS; ANTINUCLEAR ANTIBODIES; CLINICAL ASSOCIATIONS; RHEUMATOID-ARTHRITIS; IMMUNOGENETIC ASSOCIATIONS; MULTICENTER VALIDATION; LUPUS-ERYTHEMATOSUS; REVISED CRITERIA;
D O I
10.1016/j.jim.2012.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Detection of systemic sclerosis-associated antibodies (SSc-Ab) in routine clinical practice is mostly restricted to anti-centromere and anti-topoisomerase-I antibodies. However, also other SSc-Ab (e.g. anti-RNA-polymerase-III, anti-PM/Scl, anti-fibrillarin and anti-Th/To) have been shown to be valuable diagnostic and prognostic markers for the disease, but testing methodologies for their detection are laborious and time-consuming. This study aimed to optimize interpretational criteria of a multiparameter lineblot (LB) for the parallel detection of SSc-Ab. We also assessed its global diagnostic value as an alternative for combined conventional techniques (CCT) in the serological workup of systemic sclerosis (SSc) patients. Methods: The presence of SSc-Ab (anti-centromere, anti-topoisomerase-I, anti-RNA-polymerase-III, anti-PM/Scl, anti-fibrillarin and anti-Th/To) was identified by LB on 145 consecutive SSc patients and on 277 disease controls. Diagnostic sensitivity and specificity were calculated for both individual reactivities and the global LB. Cohen's kappa coefficient was used to examine agreement between LB and CCT and guided the definition of final interpretational criteria for LB. Results: Applying the optimal cut-off values and interpretational criteria. LB identified SSc-Ab in 110 SSc patients (sensitivity = 76%) and in 19 disease controls (specificity = 93%). Globally, there was a substantial agreement between CCT and LB (kappa = 0.787, concordance 92.4%). LB and CD' showed a very good correlation (kappa > 0.800) for most SSc-Ab (anti-centromere, anti-topoisomerase-I, anti-RNA-polymerase-III and anti-PM/Scl). The best agreement for anti-RNApolymerase-III and anti-PM/Scl was achieved when positivity for both components was taken as a criterion. Conclusions: LB is a reliable alternative for the laborious and time-consuming conventional techniques in the diagnostic workup of SSc, especially for the detection of anti-centromere, anti-topoisomerase-I, anti-RNA-polymerase-III and anti-PM/Scl. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 60
页数:8
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