Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients
Background: The diagnosis of early rheumatoid arthritis (RA) is challenging. B-cell chemokine (CXCL13) plays a critical role in the disease pathogenesis. Aim of the work: To assess the diagnostic value of serum CXCL13 in early RA and compare it with rheumatoid factor (RF) and anti-cyclic citrullinat...
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doaj-5d50085beb6e47098db09aec93fc521a2020-11-25T02:16:39ZengElsevierEgyptian Rheumatologist1110-11642019-01-014111114Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patientsShadia I. Allam0Rehab A. Sallam1Doaa M. Elghannam2Atif I. El-Ghaweet3Rheumatology and Rehabilitation Department, Faculty of Medicine, Mansoura University, Al-Dakahlya, EgyptRheumatology and Rehabilitation Department, Faculty of Medicine, Mansoura University, Al-Dakahlya, Egypt; Corresponding author.Clinical Pathology Department, Faculty of Medicine, Mansoura University, Al-Dakahlya, EgyptRheumatology and Rehabilitation Department, Faculty of Medicine, Mansoura University, Al-Dakahlya, EgyptBackground: The diagnosis of early rheumatoid arthritis (RA) is challenging. B-cell chemokine (CXCL13) plays a critical role in the disease pathogenesis. Aim of the work: To assess the diagnostic value of serum CXCL13 in early RA and compare it with rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibodies. Patients and methods: The study included 60 RA patients; 30 early, 30 established RA and 30 healthy controls. The modified health assessment questionnaire (MHAQ), modified Sharp-van der Heijde score (MSS) and disease activity score (DAS28) were assessed in RA patients. RF, anti-CCP and serum level of CXCL13 were measured. Results: Patients had a mean age of 39 ± 7.4 years and disease duration of 4.4 ± 5.7 years; they were 46 females and 12 males (F:M 3.8:1). Serum CXCL13 was significantly higher in early (191.7 ± 74.4 pg/ml) compared to established (136.4 ± 79 pg/ml) RA (p = 0.007) which were not observed with RF and anti-CCP; both were higher than in control (30.4 ± 13.5 pg/ml) (p < 0.001). In early RA, the frequencies of CXCL13, RF and anti-CCP positivity were 90%, 73.3% and 56.7% while in the established cases the frequencies were 36.7%, 66.7% and 63.3% respectively. CXCL13 significantly correlated with DAS28 (early: 0.49, p = 0.006; established: r = 0.38, p = 0.04) but not with MHAQ or MSS. The CXCL13 significantly correlated with both the RF and anti-CCP in both early and established cases (p < 0.001). Conclusion: CXCL13 is an important for the diagnosis of early RA with a superior diagnostic performance compared to RF and anti-CCP. It may also be considered a potential biomarker of disease activity. Keywords: Rheumatoid arthritis, Diagnosis, CXCL13, Anti-CCP, Rheumatoid factorhttp://www.sciencedirect.com/science/article/pii/S1110116418300590 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shadia I. Allam Rehab A. Sallam Doaa M. Elghannam Atif I. El-Ghaweet |
spellingShingle |
Shadia I. Allam Rehab A. Sallam Doaa M. Elghannam Atif I. El-Ghaweet Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients Egyptian Rheumatologist |
author_facet |
Shadia I. Allam Rehab A. Sallam Doaa M. Elghannam Atif I. El-Ghaweet |
author_sort |
Shadia I. Allam |
title |
Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients |
title_short |
Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients |
title_full |
Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients |
title_fullStr |
Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients |
title_full_unstemmed |
Clinical significance of serum B cell chemokine (CXCL13) in early rheumatoid arthritis patients |
title_sort |
clinical significance of serum b cell chemokine (cxcl13) in early rheumatoid arthritis patients |
publisher |
Elsevier |
series |
Egyptian Rheumatologist |
issn |
1110-1164 |
publishDate |
2019-01-01 |
description |
Background: The diagnosis of early rheumatoid arthritis (RA) is challenging. B-cell chemokine (CXCL13) plays a critical role in the disease pathogenesis. Aim of the work: To assess the diagnostic value of serum CXCL13 in early RA and compare it with rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibodies. Patients and methods: The study included 60 RA patients; 30 early, 30 established RA and 30 healthy controls. The modified health assessment questionnaire (MHAQ), modified Sharp-van der Heijde score (MSS) and disease activity score (DAS28) were assessed in RA patients. RF, anti-CCP and serum level of CXCL13 were measured. Results: Patients had a mean age of 39 ± 7.4 years and disease duration of 4.4 ± 5.7 years; they were 46 females and 12 males (F:M 3.8:1). Serum CXCL13 was significantly higher in early (191.7 ± 74.4 pg/ml) compared to established (136.4 ± 79 pg/ml) RA (p = 0.007) which were not observed with RF and anti-CCP; both were higher than in control (30.4 ± 13.5 pg/ml) (p < 0.001). In early RA, the frequencies of CXCL13, RF and anti-CCP positivity were 90%, 73.3% and 56.7% while in the established cases the frequencies were 36.7%, 66.7% and 63.3% respectively. CXCL13 significantly correlated with DAS28 (early: 0.49, p = 0.006; established: r = 0.38, p = 0.04) but not with MHAQ or MSS. The CXCL13 significantly correlated with both the RF and anti-CCP in both early and established cases (p < 0.001). Conclusion: CXCL13 is an important for the diagnosis of early RA with a superior diagnostic performance compared to RF and anti-CCP. It may also be considered a potential biomarker of disease activity. Keywords: Rheumatoid arthritis, Diagnosis, CXCL13, Anti-CCP, Rheumatoid factor |
url |
http://www.sciencedirect.com/science/article/pii/S1110116418300590 |
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