학술논문

Non-invasive imaging and clinical skin scores in juvenile localized scleroderma.
Document Type
Article
Source
Rheumatology. May2024, Vol. 63 Issue 5, p1332-1340. 9p.
Subject
*SKIN temperature
*RESEARCH funding
*SKIN
*SCLERODERMA (Disease)
*LONGITUDINAL method
*REACTIVE oxygen species
*OXYGEN in the body
Language
ISSN
1462-0324
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). [ABSTRACT FROM AUTHOR]