CORRELATION OF SEROLOGIC INDICATORS OF INFLAMMATION WITH EFFECTIVENESS OF NONSTEROIDAL ANTIINFLAMMATORY DRUG-THERAPY IN RHEUMATOID-ARTHRITIS

被引:55
作者
CUSH, JJ
LIPSKY, PE
POSTLETHWAITE, AE
SCHROHENLOHER, RE
SAWAY, A
KOOPMAN, WJ
机构
[1] UNIV ALABAMA,MED CTR,BIRMINGHAM,AL 35294
[2] UNIV TENNESSEE,CTR HLTH SCI,COLL MED,MEMPHIS,TN 38163
[3] UNIV TEXAS,SW MED CTR,HAROLD C SIMMONS ARTHRITIS RES CTR,DALLAS,TX 75235
[4] VET ADM MED CTR,BIRMINGHAM,AL
来源
ARTHRITIS AND RHEUMATISM | 1990年 / 33卷 / 01期
关键词
D O I
10.1002/art.1780330103
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Forty‐seven patients with rheumatoid arthritis (mean duration 5.7 years) who were receiving neither disease‐modifying drugs nor corticosteroids were enrolled in a 12‐week, multicenter study of the relationship between clinical and serologic measures of disease activity in patients taking nonsteroidal antiinflammatory drugs. After a 2‐week drug washout period, patients received flurbiprofen (200 mg/day) or sustained‐release ibuprofen (2,400 mg/day) for a 10‐week trial. Clinical response was assessed biweekly using standard clinical parameters, including 50‐foot walk time, tender joint score, duration of morning stiffness, and global assessment of disease activity and pain (by both the patient and the physician). Patients were classified as responders if there was ⩾30% improvement in at least 3 of the 4 clinical measures of disease activity. Thirty patients completed at least 8 weeks of therapy; there were 12 responders and 18 nonresponders. Of the laboratory parameters examined, the responders, but not the nonresponders, demonstrated significant reductions (from postwashout values) in levels of IgM rheumatoid factor and C‐reactive protein (CRP), along with significant increases in the number of circulating lymphocytes and decreases in the number of circulating granulocytes (P ⩽ 0.05). In contrast, the nonresponders demonstrated either no change or worsening of the laboratory correlates of disease activity. The responders also appeared to have more aggressive disease at baseline, with significantly more painful joints, greater 50‐foot walk times, elevated CRP values, and elevated erythrocyte sedimentation rates (P ⩽ 0.05). These data suggest that there is a subset of rheumatoid arthritis patients in whom clinical improvement with nonsteroidal antiinflammatory drug therapy is associated with significant reductions in IgM rheumatoid factor and CRP levels. Copyright © 1990 American College of Rheumatology
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页码:19 / 28
页数:10
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共 33 条
  • [1] THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS
    ARNETT, FC
    EDWORTHY, SM
    BLOCH, DA
    MCSHANE, DJ
    FRIES, JF
    COOPER, NS
    HEALEY, LA
    KAPLAN, SR
    LIANG, MH
    LUTHRA, HS
    MEDSGER, TA
    MITCHELL, DM
    NEUSTADT, DH
    PINALS, RS
    SCHALLER, JG
    SHARP, JT
    WILDER, RL
    HUNDER, GG
    [J]. ARTHRITIS AND RHEUMATISM, 1988, 31 (03): : 315 - 324
  • [2] Aylward M, 1975, Rheumatol Rehabil, V14, P101, DOI 10.1093/rheumatology/14.2.101
  • [3] BEUTLER B, 1987, NEW ENGL J MED, V316, P379
  • [4] IBUPROFEN OR ASPIRIN IN RHEUMATOID-ARTHRITIS THERAPY
    BLECHMAN, WJ
    SCHMID, FR
    APRIL, PA
    WILSON, CH
    BROOKS, CD
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1975, 233 (04): : 336 - 340
  • [5] IMMUNOMODULATORY EFFECTS OF TREATMENT WITH NAPROXEN IN PATIENTS WITH RHEUMATIC DISEASE
    CEUPPENS, JL
    ROBAEYS, G
    VERDICKT, W
    VERTESSEN, S
    DECKMYN, H
    DEQUEKER, J
    [J]. ARTHRITIS AND RHEUMATISM, 1986, 29 (03): : 305 - 311
  • [6] CEUPPENS JL, 1982, LANCET, V1, P528
  • [7] PHENOTYPIC ANALYSIS OF SYNOVIAL TISSUE AND PERIPHERAL-BLOOD LYMPHOCYTES ISOLATED FROM PATIENTS WITH RHEUMATOID-ARTHRITIS
    CUSH, JJ
    LIPSKY, PE
    [J]. ARTHRITIS AND RHEUMATISM, 1988, 31 (10): : 1230 - 1238
  • [8] DAWES PT, 1986, BRIT J RHEUMATOL, V25, P44
  • [9] DEVRIES E, 1986, RHEUMATOL INT, V4, P91
  • [10] AN UPDATE ON HUMAN INTERLEUKIN-1 - FROM MOLECULAR-BIOLOGY TO CLINICAL RELEVANCE
    DINARELLO, CA
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 1985, 5 (05) : 287 - 297