Key result
Erythromelalgia is linked to ~47% weaker sympathetic vasoconstrictor responses to cold challenge at the toe.
Why the study?
Patients with erythromelalgia have enhanced cutaneous vascular tone at rest and during stimulation, suggesting increased sympathetic neural activity, but their skin vasoconstrictor responses to sympathetic stimuli were not well characterized.
Do patients with erythromelalgia have altered skin vasoconstrictor responses to cold challenge and inspiratory gasp compared to controls?
Case-Control
Do patients with erythromelalgia have altered skin vasoconstrictor responses to cold challenge and inspiratory gasp compared to controls?
Absolute Event Rate: 0.37% vs 0.7%
p-value: p=<0.001
Patients with erythromelalgia have diminished sympathetic vasoconstrictor responses to cold challenge and inspiratory gasp, suggesting an interplay between neural and vasoactive agents in its pathophysiology.
Suggests sympathetic involvement in erythromelalgia; hypothesis-generating and should not yet change practice.
Erythromelalgia (EM) is a chronic disorder characterized by intermittent burning pain, warmth and erythema of the extremities. Increasing the local temperature and dependency of the affected limb(s) precipitates the symptoms, whereas direct cooling and elevation of the limb(s) can provide partial relief. Our previous findings showed that patients with EM have enhanced cutaneous vascular tone at rest and during stimulation, which may be due to an increase in sympathetic neural activity. To test this, we measured skin vasoconstrictor responses to contralateral arm cold challenge (CC) and inspiratory gasp (IG) using laser Doppler flowmetry at the toe pulp and fingertip. These areas were chosen because of their dense sympathetic innervation. An index of the vasoconstrictor response (between 0 and 1) was calculated from the change in skin perfusion from baseline following CC and IG. In control subjects, vasoconstrictor responses to CC at the toe and fingertip were both 0. 70+/-0.02 (mean+/-S.E.M.), which were significantly greater (P<0. 001) than corresponding values in patients with EM (0.37+/-0.04 and 0.45+/-0.04 respectively). Similarly, vasoconstrictor responses to IG were significantly greater (P<0.001) at the toe and fingertip in control subjects (0.70+/-0.03 and 0.70+/-0.02 respectively) compared with values in EM patients (0.27+/-0.03 and 0.45+/-0.15 respectively). These data show that, in contrast with control subjects, patients with EM have diminished sympathetic vasoconstrictor responses to both CC and IG. Denervation supersensitivity may play a part by increasing vasoconstrictor responses to circulating catecholamines, leading to a reduction in skin blood flow. Therefore an interplay between neural and vasoactive agents may be involved in the pathophysiology of EM.
No takes yet. Share an insight, caveat, or question.
Littleford et al. (1999) conducted a case-control in Erythromelalgia. Erythromelalgia vs. Control subjects was evaluated on Vasoconstrictor response to contralateral arm cold challenge (CC) at the toe (p=<0.001). Patients with erythromelalgia had significantly diminished sympathetic vasoconstrictor responses to cold challenge at the toe compared with control subjects (0.37 vs 0.70; P<0.001).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: