Prediction of disease progression in early rheumatoid arthritis by ICTP, RF land CRP.: A comparative 3-year follow-up study

被引:35
作者
Åman, S
Paimela, L
Leirisalo-Repo, M
Risteli, J
Kautiainen, H
Helve, T
Hakala, M [1 ]
机构
[1] Univ Oulu, Dept Internal Med, Div Rheumatol, FIN-90220 Oulu, Finland
[2] Invalid Fdn, Orton Rehabil Ctr, Helsinki, Finland
[3] Univ Helsinki, Cent Hosp, Dept Med, Div Rheumatol, Helsinki, Finland
[4] Univ Oulu, Dept Clin Chem, Oulu, Finland
[5] Rheumatism Fdn Hosp, SF-18120 Heinola, Finland
[6] Helsinki City Hosp, Helsinki, Finland
基金
芬兰科学院;
关键词
prognosis; joint destruction; collagen degradation; ICTP; C-reactive protein; rheumatoid factor; rheumatoid arthritis;
D O I
10.1093/rheumatology/39.9.1009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To test the predictive value of the cross-linked carboxyterminal telopeptide of type I collagen (ICTP; a marker of type I collagen degradation), rheumatoid factor (RF) and C-reactive protein (CRP) for disease progression in patients with early rheumatoid arthritis (RA) Method. We tested the value of baseline values of RF, CRP and ICTP for the prediction of radiological joint progression over 3 yr in 63 consecutive patients with early RA who were treated with the 'saw-tooth strategy'. Results. Age- and sex-adjusted risks as odds ratios (95% confidence intervals) of elevated serum ICTP, RF positivity and increased CRP for progressive joint disease (defined as an increase of >20 in Larsen's index on radiographs of the hands and feet) were 3.9 (1.3, 11.9), 3.9 (1.0, 15.5) and 2.6 (0.9, 7.5), respectively. Better prediction was achieved when the tests were used in combination, and where there was both elevated ICTP and positive RF the odds ratio was 9.1 (2.5, 32.9). This test combination showed good sensitivity and specificity (71 and 77%, respectively), with a positive predictive value of 65% and a likelihood ratio of 3.1. Conclusion. This kind of risk profile, in which the tests used reflect different aspects of the disease process, may be useful in early disease assessment to find patients who will need the most active drug therapy.
引用
收藏
页码:1009 / 1013
页数:5
相关论文
共 29 条
  • [21] THE PROGNOSTIC VALUE OF HLA-DR4 AND HLA-B27 ANTIGENS IN EARLY RHEUMATOID-ARTHRITIS
    PAIMELA, L
    LEIRISALOREPO, M
    HELVE, T
    KOSKIMIES, S
    [J]. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 1993, 22 (05) : 220 - 224
  • [22] MARKERS OF BONE AND COLLAGEN BREAKDOWN IN EARLY INFLAMMATORY ARTHRITIS
    PEEL, N
    EASTELL, R
    RUSSELL, G
    [J]. BAILLIERES CLINICAL RHEUMATOLOGY, 1992, 6 (02): : 351 - 372
  • [23] RISTELI J, 1993, CLIN CHEM, V39, P635
  • [24] RITCHIE DM, 1968, Q J MED, V37, P393
  • [25] Immunochemical characterization of assay for carboxyterminal telopeptide of human type I collagen: Loss of antigenicity by treatment with cathepsin K
    Sassi, ML
    Eriksen, H
    Risteli, L
    Niemi, S
    Mansell, J
    Gowen, M
    Risteli, J
    [J]. BONE, 2000, 26 (04) : 367 - 373
  • [26] SCOTT DL, 1995, BRIT J RHEUMATOL, V34, P56
  • [27] St Clair EW, 1998, J RHEUMATOL, V25, P1472
  • [28] RADIOGRAPHIC ASSESSMENT IN RELATION TO CLINICAL AND BIOCHEMICAL VARIABLES IN RHEUMATOID-ARTHRITIS
    WOLLHEIM, FA
    PETTERSSON, H
    SAXNE, T
    SJOBLOM, KG
    [J]. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 1988, 17 (06) : 445 - 453
  • [29] Can we predict aggressive disease?
    Young, A
    vanderHeijde, DMFM
    [J]. BAILLIERES CLINICAL RHEUMATOLOGY, 1997, 11 (01): : 27 - 48