Korendowych E, Owen P, Ravindran J, Carmichael C, McHugh N
Royal National Hospital for Rheumatic Diseases, Upper Borough Walls, Bath BA1 1RL, UK.
Rheumatology (Oxford). 2005 Aug;44(8):1056-60. doi: 10.1093/rheumatology/keh686. Epub 2005 May 18.
Antibodies recognizing a cyclic citrullinated peptide (anti-CCP) are highly specific for rheumatoid arthritis (RA) but their role in psoriatic arthritis (PsA) remains unclear. The aim of this study was therefore to investigate the prevalence of anti-CCP antibodies in PsA and assess their clinical and genetic associations.
One hundred and twenty-six patients with PsA, 40 patients with seropositive RA and 40 controls were tested for the presence of anti-CCP antibodies, rheumatoid factor (RF) and the HLA-DRB1 shared epitope. Clinical and radiological data were collected prospectively on all patients and compared between anti-CCP-positive and -negative patients.
Seven (5.6%) patients with PsA were positive for anti-CCP antibodies compared with 0% of controls and 97% of patients with seropositive RA. The presence of anti-CCP antibodies in PsA was significantly associated with the HLA-DRB1 shared epitope (P<0.005), erosive disease (P<0.05), number of swollen joints (P<0.02) and DMARD use (P<0.05).
Overall, the increased prevalence of anti-CCP antibodies in this PsA population failed to reach statistical significance. However, when present, they were a marker of disease severity and had RA-linked MHC class II associations. Further studies are needed in a larger population of patients with PsA and appropriate controls to confirm any true association that may be present.
识别环瓜氨酸肽的抗体(抗CCP抗体)对类风湿关节炎(RA)具有高度特异性,但其在银屑病关节炎(PsA)中的作用仍不明确。因此,本研究旨在调查PsA患者中抗CCP抗体的患病率,并评估其临床和遗传相关性。
对126例PsA患者、40例血清阳性RA患者和40例对照者检测抗CCP抗体、类风湿因子(RF)和HLA - DRB1共享表位的存在情况。前瞻性收集所有患者的临床和放射学数据,并在抗CCP抗体阳性和阴性患者之间进行比较。
7例(5.6%)PsA患者抗CCP抗体呈阳性,而对照者为0%,血清阳性RA患者为97%。PsA患者中抗CCP抗体的存在与HLA - DRB1共享表位(P<0.005)、侵蚀性疾病(P<0.05)、肿胀关节数量(P<0.02)和使用改善病情抗风湿药(DMARD)(P<0.05)显著相关。
总体而言,该PsA人群中抗CCP抗体患病率的增加未达到统计学意义。然而,当抗CCP抗体存在时,它们是疾病严重程度的标志物,并与RA相关的MHC II类存在关联。需要在更大规模的PsA患者群体和适当对照中进行进一步研究,以确认可能存在的任何真正关联。