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Table 2 Clinical characteristics and treatments of the RA-CAD and pure RA groups

From: Reduction of peripheral regulatory T cells in active rheumatoid arthritis patients with coronary artery disease

 

RA-CAD (n = 54)

RA (n = 43)

p value

Morning stiffness > 1 h

32 (59.3%)

21 (48.8%)

NS

Dry mouth (%)

25 (46.3%)

19 (44.2%)

NS

Dry eye (%)

12 (22.2%)

11 (25.6%)

NS

Back pain (%)

8 (14.8%)

5 (11.6%)

NS

Treated/untreated

33/21

28/15

NS

GCs (prednisone 2.5–10mgday) (%)

19/54 (35.2%)

18/43 (41.9%)

NS

DMARDs (MTX/LEF/HCQ) (%)

23/54 (42.6%)

18/43 (41.9%)

NS

NSAIDs (%)

16/54 (29.6%)

15/43 (34.9%)

NS

Biologics (rhTNFR-Fc) (%)

5/54 (9.3%)

1/43 (2.3%)

NS

Statins (%)

32/54 (59.3%)

–

–

Anti-platelet drug (%)

25/54 (46.3%)

–

–

Beta-blockers (%)

9/54 (16.7%)

–

–

ACEI/ARBs (%)

4/54 (7.4%)

–

–

Coronary-expansion drugs (%)

10/54 (18.5%)

–

–

  1. Data are number (n)/percentage (%) and were measured using the chi-square test
  2. NS; Not significant; GCs: glucocorticoids; DMARDs: disease-modifying antirheumatic drugs; NSAIDs: nonsteroidal anti-inflammatory drugs; MTX: methotrexate; LEF: leflunomide; HCQ: Hydroxychloroquine; rhTNFR-Fc: recombinant human tumor necrosis factor-α receptor II: IgG Fc fusion protein for injection