Table 1

Description of features of patients with polymyalgia rheumatica (PMR) with and without characteristic extracapsular pattern of inflammation

Extracapsular pattern (n=14)Non-extracapsular pattern (n=8)p Value
Demographics
 Age, median (range)75 (55, 85)78 (70, 84)0.22
 Male, n (%)8 (57%)0 (0%)0.02
Acute-phase markers
 ESR, median (range), mm/h46 (9, 119)38 (4, 81)0.63
 CRP, median (range), mg/L36 (5, 118)5.25 (5, 76)0.03
 PV, median (range), mPa s1.93 (1.78, 2.12)1.81 (1.57, 2.04)0.36
 IL-6, median (range), pg/mL25.8 (0.3, 87.6)6.0 (0.2, 131.5)*0.04
Composite disease activity scores
 PMR-AS (median, IQR)78.6 (53.8, 103.0)70.2 (34.4, 106.1)0.73
Pretreatment patient-reported outcomes
 Pain VAS (median, IQR)7.7 (5.0, 8.1)7.9 (4.3, 8.7)0.63
 Stiffness VAS (median, IQR)6.3 (4.5, 8.0)8.2 (5.2, 8.9)0.29
 Fatigue VAS (median, IQR)7.1 (5.2, 7.6)8.4 (7.0, 9.7)0.03
 HAQ-DI (median, IQR)1.25 (1.09, 1.50)1.56 (1.28, 2.09)0.07
Assessment of glucocorticoid responsiveness at first follow-up
 ‘I feel back to normal since taking steroids’. n (%)11/13 (85%)1/6 (17%)0.01
 ‘I feel [or felt] back to normal since taking steroids’. n (%)12/14 (86%)1/8 (13%)0.001
 Fatigue VAS at follow-up (median, IQR)1.3 (0.2, 3.8)7.1 (3.6, 9.8)0.02
 HAQ-DI at follow-up (median, IQR)0 (0, 0.625)1.0 (0.76, 2.07)0.003
Prognosis
 Stopped glucocorticoids permanently after <1 year†1/144/70.03
 Relapse-free†7/142/81.00
 Relapsed when on 5 mg or more†3/143/70.35
 Required initial dose increase >15 mg2/141/81.00
  • The PMR-AS is the PMR Activity Score as described by Bird and Leeb. Either Mann–Whitney U test or Fisher's exact test was used for non-normally distributed values; unpaired t test for normally distributed variables. All tests were two-tailed. Apart from glucocorticoid responsiveness (the a priori hypothesis), p values should be interpreted in the light of multiple testing. Bonferroni correction for all the variables reported here (likely over-stringent because of strong correlation between ESR/CRP/PV/IL-6 and between patient-reported VAS scores) would require a threshold of 0.05/19, or p<0.0026.

  • *Excludes one patient who did not have IL-6 measured.

  • †Excludes one patient who was lost to follow-up at 4 months.

  • CRP, C-reactive protein; IL-6, interleukin-6; PV, plasma viscosity; VAS, visual analogue score.