Table 3

Studies reporting on age, sex, AIM subsets, disease activity/course and pain

StudyDisease duration (years)Disease activityPain severity*Findings
SF-36 BP (additive 0–100, norm-based mean 50, SD 10); lower score, more pain
Sultan et al26N/AActive disease 21%Mean
55
Significantly higher pain in chronic progressive illness compared with relapsing–remitting course (p<0.05), no difference between active and inactive disease
Ponyi et al28Median (range)
8.9 (3.0–22.8)
Active disease 13%Mean±SD
DM: 54±18
PM: 58±20
OM: 66±18
No significant differences in pain between AIM subsets or disease course. No correlation with disease activity. Predictors of more pain: female (β=−15.5, p=0.00), disease duration <5 years (β=−14.2, p=0.001), arthralgias (β=−11.6, p=0.005) and compression fracture/AVN (β−23.9, p=0.002)
Sadjadi et al29Mean±SD
4.4±3
N/AMean±SD
69±27
No significant correlation of pain with age or disease duration, moderate correlation with Beck Depression Inventory scores (values not reported)
Goreshi et al23N/ACDASI (0–100): 20±11Norm-based
Mean: 50
No significant correlation between pain and PtGA (r=0.296, p=0.67)
Regardt et al32Mean±SD
6.8±5.5
N/AMean±SD
All: 58
DM:55
PM: 58
No significant differences in pain between sex or AIM subsets
Xu et al43Median (IQR)
5 (2.5–7.4)
VAS score (0–100)
Median (IQR)
PhGA: 17 (5–31)
PtGA: 29 (11–49)
Mean±SD
63±26
No significant differences in pain with age, sex, disease duration or AIM subsets; pain correlated weakly with MMT-8 (r=0.30, p=0.03) and moderately with PtGA (r=−0.62, p<0.001); no significant correlation with PhGA
van de Vlekkert et al35Median*
baseline: 0.3
Early active diseaseMean
42
No difference in pain between AIM subsets
Landon-Cardinal et al40Mean±SD
DM: 3±2
IMNM: 9±8
OM: 3±4
VAS score (0–10), mean±SDMean±SD
All: 65±26
DM: 55±24
IMNM: 71±24
OM: 63±28
No significant difference in pain at baseline between AIM subsets
DMPhGA: 3±2
IMNMPhGA: 2±2
OMPhGA: 3±3
HAQ-Pain Index (0–3); higher score, more pain
Christopher-Stine et al18Mean±SD
8±7
In year prior, no flare 22%, 1–3 flares 47%, >4 flares 26%Mean±SD
1.04±0.87
Higher mean±SD HAQ-Pain Index scores with increased flare frequency (no flare 0.69±0.83, 1–3 flares 1.02±0.84, >4 flares 1.52±0.78 (p<0.001))
INQOL score; higher score, more pain
Rose et al33N/AN/AMean±SD
PM/DM: 70±19
IBM: 46±29
All NMD: 42±27
Pain in NMD significantly correlated (p<0.01) with anxiety (r=0.33), depression (r=0.41) and many IPQ-R domains: identity (r=0.43), consequences (r=0.3), illness coherence (r=0.23), timeline cyclical (r=0.32) and emotional (r=0.35)
NHP score (0–100); higher score, more pain
Chung et al19Mean (range)
DM: 7 (1–26)
PM: 7 (1–27)
Acute cases excludedMean±SD
All: 30±32
DM: 30±31
PM: 31±33
Worse energy scores were associated with worse pain (β=0.2, p=0.03)
VAS score (0–100); higher score, more pain
Mahler et al31Median (IQR)
4 (2.5–6.5)
VAS score (0–100)
Mean±SD
PhGA: 55±8
Mean±SD
21±21
After rituximab treatment, pain not significantly reduced while disease activity improved.
Opinc et al38<1 year: 13%
1–5 years: 40%
>5 years: 47%
N/AMean±SD
DM: 37±28
PM: 39±29
OM: 38±33
IBM: 22±27
Pain in IBM significantly lower than other AIM subsets (p<0.05). Mean myalgia value (VAS, 0–10) significantly lower in IBM (3±2) compared with DM (4±2), PM (4±2) and OM (4±2) (p<0.001).
  • *If not shown, measure of dispersion not provided.

  • AIM, autoimmune inflammatory myopathy; DM, dermatomyositis; HAQ, Health Assessment Questionnaire; IBM, inclusion body myositis; IMNM, immune-mediated necrotising myopathy; INQOL, Individualised Neuromuscular Quality of Life Questionnaire; IPQ-R, Illness Perceptions Questionnaire-Revised; MMT-8, Manual Muscle Testing-8; N/A, not available; NHP, Nottingham Health Profile; NMD, neuromuscular disease; OM, overlap myositis; PhGA, Physician Global Assessment; PM, polymyositis; PtGA, Patient Global Assessment; SF-36 BP, 36-Item Short Form Bodily Pain; VAS, visual analogue scale.