Non-invasive imaging and clinical skin scores in juvenile localized scleroderma

Author:

Pain Clare E12ORCID,Murray Andrea34ORCID,Dinsdale Graham4ORCID,Marsden Antonia5,Manning Joanne4,Riley Phil6,Leone Valentina7,Amin Tania8,Zulian Francesco9ORCID,Herrick Ariane L34ORCID

Affiliation:

1. Department of Rheumatology, Alder Hey Children’s NHS Foundation Trust , Liverpool, UK

2. Department of Women’s and Children’s Health, Institute of Life Course and Medical Sciences, University of Liverpool , Liverpool, UK

3. Division of Musculoskeletal and Dermatological Sciences, University of Manchester , Manchester, UK

4. Department of Rheumatology, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre , Manchester, UK

5. Division of Population Health, Health Services Research and Primary Care, University of Manchester , Manchester, UK

6. Department of Paediatric Rheumatology, Central Manchester University Hospitals NHS Foundation Trust , Manchester, UK

7. Department of Pediatrics, Istituto Mediterraneo per i Trapianti Ismett IRCCS , Palermo, Sicily, Italy

8. Department of Paediatric Rheumatology, Leeds Teaching Hospital NHS Trust , Leeds, UK

9. Department of Women’s and Child’s Health, University Hospital of Padua , Padua, Italy

Abstract

Abstract Objectives To evaluate whether in juvenile localized scleroderma (JLS), non-invasive imaging can differentiate affected from non-affected skin and whether imaging correlates with a validated skin score [Localised Scleroderma Cutaneous Assessment Tool (LoSCAT)]. Methods A total of 25 children with JLS were recruited into a prospective study and a single ‘target’ lesion was selected. High-frequency ultrasound (HFUS, measuring skin thickness), infrared thermography (IRT, skin temperature), laser Doppler imaging (LDI, skin blood flow) and multispectral imaging (MSI, oxygenation) were performed at four sites: two of affected skin (centre and inner edge of lesion) and two of non-affected skin (1 cm from the edge of the lesion ‘outer’ and contralateral non-affected side) at four visits at 3 month intervals. Results Differences between affected and non-affected skin were detected with all four techniques. Compared with non-affected skin, affected skin was thinner (P < 0.001), with higher temperature (P < 0.001–0.006), perfusion (P < 0.001–0.039) and oxygenation (P < 0.001–0.028). Lesion skin activity (LoSCAT) was positively correlated with centre HFUS [r = 0.32 (95% CI 0.02, 0.61), P = 0.036] and negatively correlated with centre LDI [r = −0.26 (95% CI −0.49, −0.04), P = 0.022]. Lesion skin damage was positively correlated with centre and inner IRT [r = 0.43 (95% CI 0.19, 0.67), P < 0.001 and r = 0.36 (95% CI 0.12, 0.59), P = 0.003, respectively] and with centre and inner LDI [r = 0.37 (95% CI 0.05, 0.69), P = 0.024 and r = 0.41 (95% CI 0.08, 0.74), P = 0.015, respectively]. Conclusion Non-invasive imaging can detect differences between affected and non-affected skin in JLS and may help to differentiate between activity (thicker, less well-perfused skin) and damage (thinner, highly perfused skin).

Funder

Scleroderma & Raynaud’s UK

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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