Schellekens G A, Visser H, de Jong B A, van den Hoogen F H, Hazes J M, Breedveld F C, van Venrooij W J
University of Nijmegen, The Netherlands.
Arthritis Rheum. 2000 Jan;43(1):155-63. doi: 10.1002/1529-0131(200001)43:1<155::AID-ANR20>3.0.CO;2-3.
Since modern treatment of rheumatoid arthritis (RA) is shifting toward aggressive antirheumatic therapy in an early phase of the disease, diagnostic tests with high specificity are desirable. A new serologic test (anti-cyclic citrullinated peptide [anti-CCP] enzyme-linked immunosorbent assay [ELISA]) was developed to determine the presence of antibodies directed toward citrullinated peptides, using a synthetic peptide designed for this purpose.
A cyclic peptide variant that contains deiminated arginine (citrulline) was designed and used as antigenic substrate in ELISA. Test parameters and diagnostic characteristics of the test were studied in patients with and without RA, in patients with various infectious diseases, and in a group of patients from an early arthritis clinic (EAC).
Using prevalent RA and non-RA sera, the anti-CCP ELISA proved to be extremely specific (98%), with a reasonable sensitivity (68%). Also, in the EAC study group, the anti-CCP ELISA appeared to be highly specific for RA (96%). In comparison with the IgM rheumatoid factor (IgM-RF) ELISA, the anti-CCP ELISA had a significantly higher specificity (96% for CCP versus 91% for IgM-RF; P = 0.016) at optimal cut-off values. The sensitivity of both tests for RA was moderate: 48% and 54% for the anti-CCP ELISA and the IgM-RF ELISA, respectively (P = 0.36). Combination of the anti-CCP and the IgM-RF ELISAs resulted in a significantly higher positive predictive value of 91% (P = 0.013) and a slightly lower negative predictive value of 78% (P = 0.35) as compared with the use of the IgM-RF ELISA alone. The ability of the 2 tests performed at the first visit to predict erosive disease at 2 years of followup in RA patients was comparable (positive predictive value 91%).
The anti-CCP ELISA might be very useful for diagnostic and therapeutic strategies in RA of recent onset.
由于类风湿关节炎(RA)的现代治疗正朝着在疾病早期进行积极的抗风湿治疗转变,因此需要高特异性的诊断测试。开发了一种新的血清学检测方法(抗环瓜氨酸肽[抗CCP]酶联免疫吸附测定[ELISA]),使用为此目的设计的合成肽来确定针对瓜氨酸化肽的抗体的存在。
设计了一种含有脱氨精氨酸(瓜氨酸)的环肽变体,并将其用作ELISA中的抗原底物。在患有和未患有RA的患者、患有各种传染病的患者以及一组来自早期关节炎诊所(EAC)的患者中研究了该检测的测试参数和诊断特征。
使用常见的RA和非RA血清,抗CCP ELISA被证明具有极高的特异性(98%),敏感性合理(68%)。此外,在EAC研究组中,抗CCP ELISA对RA似乎具有高度特异性(96%)。与IgM类风湿因子(IgM-RF)ELISA相比,在最佳临界值时,抗CCP ELISA具有显著更高的特异性(CCP为96%,IgM-RF为91%;P = 0.016)。两种检测对RA的敏感性中等:抗CCP ELISA和IgM-RF ELISA分别为48%和54%(P = 0.36)。与单独使用IgM-RF ELISA相比,抗CCP和IgM-RF ELISA联合使用可使阳性预测值显著提高至91%(P = 0.013),阴性预测值略低至78%(P = 0.35)。在首次就诊时进行的这两种检测预测RA患者2年随访时侵蚀性疾病的能力相当(阳性预测值91%)。
抗CCP ELISA可能对近期发病的RA的诊断和治疗策略非常有用。