Anti-carbamylated protein antibodies: are they useful for the diagnosis of rheumatoid arthritis?

被引:0
|
作者
Ponchel, Frederique [1 ]
van Delft, Myrthe A. M. [2 ]
Xie, Xuanxiao [1 ]
Burska, Agata N. [1 ]
Duquenne, Laurence [1 ]
Trouw, Leendert A. [2 ,3 ]
Emery, Paul [1 ,4 ]
机构
[1] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Clin Sci Bldg L5,St James Univ Hosp Campus, Leeds LS9 7TF, W Yorkshire, England
[2] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, Leiden, Netherlands
[4] Leeds Trust Teaching Hosp, NIHR Leeds Musculoskeletal Biomed Res Ctr, Leeds, W Yorkshire, England
关键词
rheumatoid arthritis; diagnosis; autoantibodies; anti-CarP level; POSTTRANSLATIONAL MODIFICATION; POTENTIAL BIOMARKERS; CARP ANTIBODIES; RENAL-FAILURE; II COLLAGEN; AUTOANTIBODIES; IDENTIFICATION; GENERATION; PRODUCTS; SMOKING;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective ACRIEULAR-2010 classification criteria for rheumatoid arthritis (RA) rely heavily on the presence of anti-citrullinated peptide antibody (ACPA). The role of anti-carbamylated protein antibodies (anti-CarP) in this context is uncertain. We aimed to investigate the value of anti-CarP for RA classification in patients with early inflammatory arthritis. Methods Patients (n=402) were recruited from an early arthritis clinic and followed for 24 months. Healthy controls (n=95) were included. An anti-CarP ELISA was performed (aU/mL). Statistical analysis used regression and AUC analysis. Results The criteria for RA were met by 195/402 patients at inclusion; 28 developed RA during follow-up and 179 had other diagnosis (non-RA). 97/195 (49%) RA patients were anti-CarP+ (median 250 uA/mL [IQR 25-762]). In the group that progressed to RA, 7/28 (25%) were positive (82 uA/mL [13-2351) compared to non-RA (p=0.001) with 13/179 (7%) positive (26 uA/mL 15-801). Being anti-CarP+ alone was observed in 17 patients of whom 7 (41%) were RA. Levels/positivity were not associated with other parameters. Anti-CarP+ had an odds ratio (OR) 6.5 for predicting RA (OR=17.1 for ACPA+ and OR=2.5 for RF+). In ACPA- patients, anti-CarP+ was also predictive of RA (OR=2.39). Being ACPA+/anti-CarP+IRF+ had a high predictive value for RA (OR=29.9 sensitivity/specificity (sen/spe) 33%/99%, positive/negative predictive values (ppv/npv) 97%/54%), however, being ACPA+/anti-CarP+ was superior (OR=36.1 sen/spe=41%199%, ppv/npv=98%/57%) while being ACPA+IRF+ was inferior (OR= 11 .9, sen/spe=54%195%, ppv/npv=94%162%). Conclusion For RA classification, anti-CarP+ was less sensitive than ACPA, but more specific than RF. Anti-CarP+ may prove useful, classifying early arthritis patients, notably ACPA- patients.
引用
收藏
页码:146 / 150
页数:5
相关论文
共 50 条
  • [21] CHARACTERIZATION OF ANTI-CARBAMYLATED SYNOVIAL PROTEIN ANTIBODIES (ANTI-CARPS) IN RHEUMATOID ARTHRITIS PATIENTS
    Regueiro, C.
    Montes, A.
    Boveda, M. D.
    Amhaz-Escanlar, S.
    Perez-Pampin, E.
    Mera-Varela, A.
    Gonzalez, A.
    ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 : 494 - 494
  • [22] ANTI-CARBAMYLATED PROTEIN ANTIBODIES IN SYSTEMIC LUPUS ERYTHEMATOSUS: ARE THEY USEFUL?
    Kumar, Rajesh
    Cavazzana, Ilaria
    Fredi, Micaela
    Ottaviani, Roberta
    Tincani, Angela
    Franceschini, Franco
    ANNALS OF THE RHEUMATIC DISEASES, 2019, 78 : 1719 - 1719
  • [23] The isotype and IgG subclass distribution of anti-carbamylated protein antibodies in rheumatoid arthritis patients
    Myrthe A. M. van Delft
    Marije K. Verheul
    Leonie E. Burgers
    Veerle F. A. M. Derksen
    Annette H. M. van der Helm-van Mil
    Diane van der Woude
    Tom W. J. Huizinga
    René E. M. Toes
    Leendert A. Trouw
    Arthritis Research & Therapy, 19
  • [24] The isotype and IgG subclass distribution of anti-carbamylated protein antibodies in rheumatoid arthritis patients
    van Delft, Myrthe A. M.
    Verheul, Marije K.
    Burgers, Leonie E.
    Derksen, Veerle F. A. M.
    van der Helm-van Mil, Annette H. M.
    van der Woude, Diane
    Huizinga, Tom W. J.
    Toes, Rene E. M.
    Trouw, Leendert A.
    ARTHRITIS RESEARCH & THERAPY, 2017, 19
  • [25] Reply to: Anti-carbamylated protein antibodies are associated with early abatacept response in rheumatoid arthritis
    Piantoni, S.
    Bazzani, C.
    Garrafa, E.
    Fredi, M.
    Cavazzana, I.
    Franceschini, F.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2021, 39 (05) : 1144 - 1144
  • [26] ANTI-CARBAMYLATED ANTIBODIES ARE ASSOCIATED WITH TOBACCO AND POOR OUTCOMES IN RHEUMATOID ARTHRITIS
    Castellanos-Moreira, Raul
    Rodriguez-Garcia, Sebastian C.
    Ruiz, Virginia
    Camacho, Oscar
    Ramirez, Julio
    Cuervo, Andrea
    Garcia-Moreno, Cristina
    Morla, Rosa
    Gomez Puerta, Jose
    Canete, Juan D.
    Haro, Isabel
    Sanmarti, Raimon
    ANNALS OF THE RHEUMATIC DISEASES, 2019, 78 : 302 - 303
  • [27] Anti-carbamylated Protein Antibodies Positivity in Rheumatoid Arthritis and Its Association With Rheumatoid Factor and Anti-cyclic Citrullinated Protein Antibodies
    Balaji, Dhanush
    Mohanasundaram, Kavitha
    Gopalakrishnan, Karpaka Vinayakam
    Suthakaran, Prasanna Karthik
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (07)
  • [28] Association of serum anti-carbamylated protein antibodies with disease activity and bone loss in rheumatoid arthritis
    Wang, Liuqing
    Hua, Li
    Hong, Xuelian
    Chen, Fang
    Du, Hongwei
    CLINICA CHIMICA ACTA, 2023, 546
  • [29] ANTI-CARBAMYLATED PROTEIN ANTIBODIES AS A CLINICAL RESPONSE PREDICTOR IN RHEUMATOID ARTHRITIS PATIENTS TREATED WITH ABATACEPT
    Fredi, M.
    Boldini, M.
    Kumar, R.
    Piantoni, S.
    Cavazzana, I.
    Garrafa, E.
    Bazzani, C.
    Tincani, A.
    Franceschini, F.
    ANNALS OF THE RHEUMATIC DISEASES, 2019, 78 : A6 - A7
  • [30] Anti-carbamylated protein antibodies as a clinical response predictor in rheumatoid arthritis patients treated with abatacept
    Kumar, R.
    Piantoni, S.
    Boldini, M.
    Garrafa, E.
    Bazzani, C.
    Fredi, M.
    Ottaviani, R.
    Cavazzana, I
    Tincani, A.
    Franceschini, E.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2021, 39 (01) : 91 - 97