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Rheumatology Advance Access originally published online on May 16, 2006
Rheumatology 2006 45(12):1490-1496; doi:10.1093/rheumatology/kel116
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© The Author 2006. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Digital thermal hyperaemia impairment does not relate to skin fibrosis or macrovascular disease in systemic sclerosis

M. Salvat-Melis1,2, P. H. Carpentier3, C. T. Minson4, A. Boignard1, G. R. McCord4, A. Paris1,2, A. Moreau-Gaudry2 and J.-L. Cracowski1,2

1Inserm ESPRI HP2 Laboratory, EA 3745, Grenoble Medical School, 2Inserm Clinical Research Center 03, 3Vascular Medicine Department, Grenoble University Hospital, Grenoble, France and 4Department of Human Physiology, University of Oregon, Eugene, OR, USA.

Correspondence to: Jean-Luc Cracowski, M.D. Ph.D., Inserm CIC 03, Centre d'Investigation Clinique de Grenoble, CHU de Grenoble, 38043 Grenoble Cedex 09, France. E-mail: Jean-Luc.Cracowski{at}ujf-grenoble.fr

Objectives. Thermal hyperaemia is impaired in patients with systemic sclerosis (SSc). The objective of these studies was to determine whether this was consecutive to skin fibrosis, microangiopathy or macroangiopathy.

Methods. Using laser Doppler flowmetry, we first compared the thermal hyperaemia on the third left finger pad and on the left forearm in 21 patients with non-diffuse systemic sclerosis (SSc), in comparison with primary Raynaud's phenomenon and healthy volunteers. Second, we tested whether the altered thermal hyperaemia correlated to the digital pressure index at baseline, and following the thermal challenge.

Results. In the first study, thermal hyperaemia of the finger pad was impaired in terms of both amplitude and kinetics, but not on the forearm in patients with SSc. In the seven SSc patients without cutaneous fibrosis, the response was similarly altered in terms of amplitude and kinetics. In the second study, we observed a weak correlation between the digital systolic blood pressure index. However, in the 15 SSc patients tested at 44°C, the median digital systolic blood pressure index was 1.04 (0.84–1.24) at baseline vs 1.08 (0.87–1.29) at 44°C (NS), while seven of them had an abnormal response in terms of kinetic. Furthermore, only one patient showed a clear-cut decrease in digital systolic blood pressure at 44°C.

Conclusion. In patients with SSc, digital thermal hyperaemia is impaired, but does not relate to the skin fibrosis or to an associated macroangiopathy in most cases. Further studies are required to determine whether its impairment reflects a functional or structural microvascular damage.

KEY WORDS: Vasodilatation, Microcirculation, Raynaud's phenomenon, Systemic sclerosis.


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