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Table 1 Participant characteristics

From: A cross-sectional study of pain sensitivity, disease-activity assessment, mental health, and fibromyalgia status in rheumatoid arthritis

  

Whole study group

Fibromyalgia classification

  

Median (IQR) or %

Yes

No

N

 

50

24

26

Female

 

76%

75%

77%

Age

 

60 (54–69)

58 (54–66)

63 (54–70)

Current smoker

 

21%

26%

17%

Analgesia

Any

69%

71%

65%

 

Paracetamol

63%

71%

54%

 

NSAID

16%

17%

15%

 

Opiate

37%

38%

35%

DMARD

Methotrexate

59%

50%

65%

 

Sulfasalazine

22%

15%

25%

 

Other nonbiologic DMARD

36%

40%

30%

 

Combination nonbiologic DMARD

24%

29%

15%

Biologic therapy

 

12%

8%

16%

Combination therapy

31%

33%

27%

Glucocorticosteroid

 

20%

15%

21%

Pressure pain threshold

   
 

Knee

173 (119–287)

133 (58–181)**

239 (169–470)

 

Tibia

140 (98–246)

108 (61–167)**

187 (122–337)

 

Sternum

155 (85–211)

111 (70–175)**

179 (149–256)

  1. Demographics of the entire study group and a comparison between participants that did or did not satisfy fibromyalgia-classification criteria. Other nonbiologic DMARDs were azathioprine (n = 2), leflunomide (n = 4), gold (n = 3), hydroxychloroquine (n = 6), and cyclosporin (n = 3). Biologic therapies were antitumor-necrosis factor agents (n=4), rituximab (n=1), or abatacept (n=1). Combination DMARDs; two or more biologic or nonbiologic DMARDs. **P < 0.01 (compared with participants who did not satisfy criteria for fibromyalgia).