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Rheumatology Advance Access originally published online on August 10, 2007
Rheumatology 2007 46(10):1566-1569; doi:10.1093/rheumatology/kem190
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© The Author 2007. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Scleroderma patients nailfold videocapillaroscopic patterns are associated with disease subset and disease severity

P. Caramaschi, S. Canestrini, N. Martinelli, A. Volpe, S. Pieropan, M. Ferrari1, L. M. Bambara, A. Carletto and D. Biasi

Dipartimento di Medicina Clinica e Sperimentale and 1Dipartimento di Scienze Biomediche e Chirurgiche - Universitá di Verona, Italy.

Correspondence to: Paola Caramaschi, Dipartimento di Medicina Clinica e Sperimentale, Policlinico G.B. Rossi, P.le Scuro, 37134 Verona, Italy. E-mail: paola.caramaschi{at}azosp.vr.it


   Abstract

Objective. To evaluate in a large group of scleroderma patients, the association of nailfold videocapillaroscopic patterns with both demographic and clinical features.

Methods. One hundred and three Italian patients (91 women and 12 men, mean age 54.3 years, median disease duration 7 yrs, 68 with limited and 35 with diffuse subset of disease), consecutively enrolled for the study, underwent nailfold videocapillaroscopy; the microvascular alterations were classified into three different patterns, early, active and late. The nailfold videocapillaroscopic patterns were correlated with such numerous clinical features as sex, age, disease duration, disease subset, disease activity, haematochemical data, involvement of skin, heart, lung and peripheral vessels.

Results. Nailfold videocapillaroscopic patterns were significantly associated with disease subsets (P = 0.018). Severity of skin, lung, heart and peripheral vascular involvement progressively increased across nailfold videocapillaroscopic patterns, from early to late pattern (P < 0.001 for cutaneous and peripheral vascular involvement; P = 0.003 and 0.002 for lung and heart involvement, respectively) as well as homocysteine plasma levels (P = 0.02). Patients with late pattern showed an increased risk to have an active disease [OR (odds ratio) 3.50; 95% CI (confidence interval) 1.31–9.39], to present digital ulcers (OR 5.74; 95% CI 2.08–15.89) and moderate to severe skin (OR 5.28; 95% CI 1.93–14.19), heart (OR 5.75; 95% CI 2.04–16.21) and lung involvement (OR 4.41; 95% CI 1.63–11.92).

Conclusions. Our study showed that scleroderma microangiopathy correlates with disease subset and severity of peripheral vascular, skin, heart and lung involvement; patients with late pattern showed an increased risk to have an active disease and to show a moderate/severe skin or visceral involvement compared to patients with early and active patterns. Therefore nailfold videocapillaroscopy, a simple, non-invasive and non-expensive investigation, is useful in staging scleroderma patients and also provides prognostic information.

KEY WORDS: Systemic sclerosis, nailfold videocapillaroscopy

Submitted 27 February 2007; revised version accepted 20 June 2007.
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