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The prevalence and clinical associations of anticardiolipin antibodies in a large inception cohort of patients with connective tissue diseases - 11/09/11

Doi : 10.1016/S0002-9343(96)00335-X 
Peter A. Merkel, MD, MPH a, , YuChiao Chang, PhD b, Sylvia S. Pierangeli, PhD c, Karen Convery, MPH b, E. Nigel Harris, MD c, Richard P. Polisson, MD, MHS a
a From the Arthritis Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA 
b From the Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA 
c From the Division of Rheumatology, Department of Medicine, University of Louisville, Louisville, Kentucky, USA 

*Requests for reprints should be addressed to Peter A. Merkel, MD, MPH, Arthritis Unit, Bulfinch 165, Massachusetts General Hospital, Boston, Massachusetts 02114.

Abstract

Purpose

To determine the prevalence and clinical associations of anticardiolipin antibodies (aCL) in a blinded, controlled study of patients with a variety of connective tissue diseases (CTD) using a standardized aCL testing system.

Patients and methods

Anticardiolipin antibodies (IgG, IgM, and IgA) were measured by direct enzyme-linked immunosorbent assay (ELISA) in the baseline serum samples of patients enrolled in a Cooperative Study of Systematic Rheumatic Diseases (CSSRD), National Institutes of Health (NIH) supported, 5-year inception-cohort, prospective study of early rheumatic diseases: rheumatoid arthritis (RA, n = 70), systemic lupus erythematosus (SLE, n = 70), scleroderma (PSS, n = 45), myositis (PM/DM, n = 36), and early undifferentiated connective tissue disease (EUCTD, n == 165). Diagnosis was based on standardized criteria and determined at the last study visit. A nested group of patients with Sjögren's syndrome (SJ, n = 44) was also defined. Serum from 200 blood donors (BB) served as controls. Additional patients with known antiphospholipid syndrome (APS, n = 33) and ANCA-related renal vasculitis (ANCA, n = 52) were also studied. Laboratory personnel were blinded to sample diagnostic group.

Results

The prevalence of either IgG or IgM aCL among each diagnostic group was RA 15.7%, SLE 15.76%, PSS 6.7%, PM/DM 8.3%, EUCTD 9.1%, SJ 6.8%, ANCA 3.8%, and BB controls 4.0%. Prevalence of aCL was significantly different for both the RA and SLE groups versus BB controls (P <0.01) but not among other diagnostic groups. Only 2 study patients had positive tests for IgA aCL (1 with PM/DM and 1 with EUCTD) versus 15% of APS with positive IgA aCL. Study patients positive for IgG or IgM aCL were significantly more likely to have hemolytic anemia or a positive serologic test for syphilis and less likely to have Raynaud's phenomenon. However, no associations were found between aCL positivity and thrombocytopenia, seizures, renal insufficiency, presence of a positive antinuclear antibody or rheumatoid factor, subcutaneous nodules or digital ulcers.

Conclusions

Based on results from this large CSSRD inception cohort, anticardiolipin antibodies are present in approximately 16% of patients with RA or SLE but are less common in patients with PSS, PM/DM, EUCTD, SJ, and ANCA vasculitis, where their prevalence approaches that in the normal population. Few consistent clinical associations can be found among patients with CTD who are aCL positive. The complete diagnostic and prognostic importance and specificity of these antibodies remains to be fully determined.

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** Dr. Merkel was supported by a Clinical Associate Physician Award from the General Clinical Research Centers Program of the National Center for Research Resources of the National Institutes of Health; Grant No. M01 RR01066.


© 1996  Publié par Elsevier Masson SAS.
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Vol 101 - N° 6

P. 576-583 - décembre 1996 Retour au numéro
Article précédent Article précédent
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