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Easy and Accurate Diagnosis of Rheumatoid Arthritis Using Anti-Cyclic Citrullinated Peptide 2 Antibody, Swollen Joint Count, and C-Reactive Protein/Rheumatoid Factor

TAKASHI YAMANE, AKIRA HASHIRAMOTO, YASUSHI TANAKA, KEN TSUMIYAMA, YASUSHI MIURA, KAZUKO SHIOZAWA, KAZUO CHIHARA, and SHUNICHI SHIOZAWA

ABSTRACT

Objective.
To determine an easy-to-use diagnostic criterion for early rheumatoid arthritis (RA) that may be useful for general physicians, using anti-cyclic citrullinated peptide (CCP) antibody.

Methods. We prospectively studied 435 patients who first visited the hospital with arthritic symptoms within 24 months, including 264 visitors within 6 months. The diagnosis was made on their first visit by examination and laboratory tests including anti-CCP antibodies, rheumatoid factor (RF) and C-reactive protein (CRP), and radiograph.

Results. The diagnostic specificity and positive predictive value (PPV) of anti-CCP2 assay were 94.9% and 87.8%, respectively, and those of anti-CCP2 plus RF were 96.9% and 90.9% for the patients who first visited having morning stiffness, arthralgia, and/or joint swelling within 3 months from onset (n = 165). For the patients who first visited later, but within 24 months from onset (n = 260), the diagnostic specificity and PPV were extremely high, 98.7% and 95.5%, when anti-CCP2 assay was coevaluated with RF, CRP, and more than 3 swollen joints. Respective combinations of anti-CCP2 assay plus either 2 of 3 measures were also highly specific.

Conclusion. A diagnostic criterion including anti-CCP2 assay in combination with RF, CRP, and/or swollen joints is less sensitive but highly specific, and accurately predicts future development of RA among those with arthritic symptoms who first consulted doctors within 2 years after onset. It should be highly useful for the general physician without special techniques or devices. (First Release Jan 15 2008; J Rheumatol 2008;35:414-20)

Key Indexing Terms:

RHEUMATOID ARTHRITIS
EARLY DIAGNOSTIC CRITERIA
ANTI-CCP ANTIBODY


From the Department of Rheumatology, Kobe University Graduate School of Medicine; Rheumatic Diseases Division, Kobe University Hospital; Division of Endocrinology/Metabolism, Neurology, and Hematology/Oncology, Department of Clinical Molecular Medicine, Kobe University Graduate School of Medicine, Kobe; and Rheumatic Disease Centre, Konan Kakogawa Hospital, Kakogawa, Japan.

T. Yamane, MD; A. Hashiramoto, MD, PhD; Y. Miura, MD, PhD; S. Shiozawa, MD, PhD, Investigator of the 21st Century Center of Excellence (COE), Japan, Department of Rheumatology, Kobe University Graduate School of Medicine and Rheumatic Diseases Division, Kobe University Hospital; K. Tsumiyama, MSc, Department of Rheumatology, Kobe University Graduate School of Medicine; Y. Tanaka, MD, PhD; K. Shiozawa, MD, PhD, Rheumatic Disease Centre, Konan Kakogawa Hospital; K. Chihara, MD, PhD, Division of Endocrinology/Metabolism, Neurology, and Hematology/Oncology, Department of Clinical Molecular Medicine, Kobe University Graduate School of Medicine.

Address reprint requests to Dr. S. Shiozawa, Department of Rheumatology, Kobe University Graduate School of Medicine, 7-10-2 Tomogaoka, Sumaku, Kobe 654-0142, Japan. E-mail: shioz@kobe-u.ac.jp

Accepted for publication October 9, 2007.




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