Interleukin‐6 positively correlates with cardiovascular disease predictor algorithms and biomarker in rheumatoid arthritis patients

Author:

Roghani Seyed Askar123,Shamsi Afsaneh1,Jalili Cyrus3,Jalili Farnaz4,Lotfi Ramin56ORCID,Garman Nima7,Rostampour Rezvan2,Taghadosi Mahdi8ORCID

Affiliation:

1. Immunology Department, Faculty of Medicine Kermanshah University of Medical Sciences Kermanshah Iran

2. Clinical Research Development Center, Imam Reza Hospital Kermanshah University of Medical Sciences Kermanshah Iran

3. Medical Biology Research Center, Health Technology Institute Kermanshah University of Medical Sciences Kermanshah Iran

4. University of Adelaide Adelaide South Australia Australia

5. Blood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran Iran

6. Clinical Research Development Center, Tohid Hospital Kurdistan University of Medical Sciences Sanandaj Iran

7. Department of Biology, Faculty of Basic Sciences University of Guilan Rasht Iran

8. Cardiovascular Research Center, Health Technology Institute Kermanshah University of Medical Sciences Kermanshah Iran

Abstract

AbstractChronic inflammation is believed as the main culprit of the link between cardiovascular disease (CVD) and rheumatoid arthritis (RA). Interleukin‐6 (IL‐6) is a pro‐inflammatory cytokine with a key role in RA pathophysiology and also correlates with joint destruction and disease activity. This study evaluates the association between IL‐6 plasma level and cardiac biomarker NT‐proBNP, HS‐CRP, CVD predictor algorithms, Framingham Risk Score (FRS) and Systematic Coronary Risk Evaluation (SCORE), as well as with CXCL9 and its receptor, CXCR3 in RA patients compared to the controls. Sixty RA patients (30 early and 30 late) and 30 healthy persons were included in this study. IL‐6 and NT‐proBNP plasma levels were measured by the ELISA. Also, HS‐CRP plasma levels were quantified using the immunoturbidimetric assay. The CVD risk was assessed by the FRS and SCORE. IL‐6 plasma levels were significantly higher in the early and late RA patients compared to the controls (p < 0.001). There was a positive correlation between IL‐6 with DAS‐28 (p = 0.007, r = 0.346), BPS (p = 0.002, r = 0.396), BPD (p = 0.046, r = 0.259), SCORE (p < 0.001, r = 0.472), and FRS (p < 0.001, r = 0.553), and a negative association with HDL (p = 0.037, r = −0.270), in the patients. Also, IL‐6 plasma level positively correlated with HS‐CRP (p = 0.021, r = 0.297) and NT‐proBNP (p = 0.045, r = 0.260) in the patients. Furthermore, a positive association was found between IL‐6 plasma levels and CXCL9 (p = 0.002, r = 0.386), and CXCR3 (p = 0.018, r = 0.304) in the patients. Given the interesting association between IL‐6 with various variables of CVD, IL‐6 may be considered a biomarker for assessing the risk for future cardiovascular events in RA patients.

Funder

Deputy for Research and Technology, Kermanshah University of Medical Sciences

Publisher

Wiley

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