Vh. Morris et al., CHARACTERIZATION OF CAPSAICIN-INDUCED MECHANICAL HYPERALGESIA AS A MARKER FOR ALTERED NOCICEPTIVE PROCESSING IN PATIENTS WITH RHEUMATOID-ARTHRITIS, Pain, 71(2), 1997, pp. 179-186
Rheumatoid arthritis (RA) is characterised by pain and tenderness not
only over inflamed or damaged joints, but also over apparently normal
tissues. Experimental models suggest that these features result from c
hanges of sensitivity within both peripheral and central neurones, but
direct evidence from human disease is lacking. At present, most clini
cal studies have evaluated overall pain experience rather than activit
y within components of the nociceptive pathway. Therefore, the aim of
this study was to assess the use of a capsaicin-based technique to qua
ntify changes of neuronal sensitivity in patients with RA. First 20 mu
l of capsaicin in solution (0.03 mg/ml) was applied topically for 30
min to apparently normal skin on the forearm of control subjects and p
atients with RA. The subsequent development of mechanical hyperalgesia
to pinprick stimuli was then measured at various time points using a
74.4-mN von Frey hair. The relationship between the area of hyperalges
ia and a number of clinical measures was determined. Capsaicin-induced
mechanical hyperalgesia was found to decline with age in normal subje
cts (r = 0.47, P < 0.01). The development of hyperalgesia had a simila
r time course in normal subjects and patients with RA. The maximum are
a of hyperalgesia, however, was substantially larger in 35 RA patients
; 254.3 +/- 20.7 cm(2), compared with 35 normal controls; 109 +/- 7.5
cm(2) (P < 0.001). An association was apparent between hyperalgesic ar
ea and a composite score of joint tenderness (r = 0.47, P < 0.01), but
not with overall pain score ora systemic marker of inflammation. Thes
e results provide evidence for enhanced sensitisation of a population
of sensory fibres in RA. Peripheral sensory activity over the forearms
of rheumatoid patients has previously been shown to be normal and the
results suggest the presence of enhanced central mechanisms in this d
isorder. The correlation between capsaicin-induced hyperalgesia and jo
int tenderness in the RA patients implies that joint symptoms arise pa
rtially as a result of central, and not exclusively peripheral, factor
s. The study supports the use of capsaicin-based techniques to explore
nociceptive mechanisms in clinical disorders characterised by chronic
pain. (C) 1997 International Association for the Study of Pain.