The Localized Scleroderma Cutaneous Assessment Tool: responsiveness to change in a pediatric clinical population
- PMID: 23562760
- PMCID: PMC3720681
- DOI: 10.1016/j.jaad.2013.02.007
The Localized Scleroderma Cutaneous Assessment Tool: responsiveness to change in a pediatric clinical population
Abstract
Background: Lack of agreement on how to accurately capture disease outcomes in localized scleroderma (LS) has hindered the development of efficacious treatment protocols. The LS Cutaneous Assessment Tool (LoSCAT), consisting of the modified LS Skin Severity Index (mLoSSI) and the LS Damage Index, has potential for use in clinical trials.
Objective: The goal of this article is to further evaluate the clinical responsiveness of the LoSCAT. Based on the modifiable nature of disease activity versus damage, we expected the mLoSSI to be responsive to change.
Methods: At 2 study visits, a physician completed the LoSCAT and Physician Global Assessment (PGA) of Disease Activity and of Disease Damage for 29 patients with LS. Spearman correlations were used to examine the relationships between the change in the LoSCAT and the PGA scores. To evaluate contrasted group validity, patients were grouped according to disease activity classification and change scores of groups were compared. Minimal clinically important differences were calculated and compared with the standard error of measurement.
Results: Change in the mLoSSI score correlated strongly with change in the PGA of Disease Activity score, whereas change in the LS Damage Index score correlated weakly with change in the PGA of Disease Damage score. The mLoSSI and PGA of Disease Activity exhibited contrasted group validity. Minimal clinically important differences for the activity measures were greater than the respective standard errors of measurement.
Limitations: Only 2 study visits were included in analysis.
Conclusion: This study gives further evidence that the LoSCAT, specifically the mLoSSI, is a responsive, valid measure of activity in LS and should be used in future treatment studies.
Keywords: CARRA; CDLQI; Childhood Arthritis and Research Alliance; Children's Dermatology Life Quality Index; ECM; LS; LoSCAT; LoSDI; Localized Scleroderma Cutaneous Assessment Tool; Localized Scleroderma Damage Index; MCID; PGA; PGA-A; PGA-D; Physician Global Assessment; Physician Global Assessment of Disease Activity; Physician Global Assessment of Disease Damage; extracutaneous manifestations; localized scleroderma; mLoSSI; measurement; minimal clinically important difference; modified Localized Scleroderma Skin Severity Index; outcomes; responsiveness to change; validity.
Copyright © 2013 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.
Conflict of interest statement
The authors have no conflict of interest to declare.
Similar articles
-
Development and initial validation of the localized scleroderma skin damage index and physician global assessment of disease damage: a proof-of-concept study.Rheumatology (Oxford). 2010 Feb;49(2):373-81. doi: 10.1093/rheumatology/kep361. Epub 2009 Dec 14. Rheumatology (Oxford). 2010. PMID: 20008472 Free PMC article.
-
Using the Localized Scleroderma Cutaneous Assessment Tool (LoSCAT) to classify morphoea by severity and identify clinically significant change.Br J Dermatol. 2020 Feb;182(2):398-404. doi: 10.1111/bjd.18097. Epub 2019 Aug 14. Br J Dermatol. 2020. PMID: 31049928
-
Reliability of LoSCAT score for activity and tissue damage assessment in a large cohort of patients with Juvenile Localized Scleroderma.Pediatr Rheumatol Online J. 2018 Jun 18;16(1):37. doi: 10.1186/s12969-018-0254-9. Pediatr Rheumatol Online J. 2018. PMID: 29914516 Free PMC article.
-
Endpoints and outcomes for localized scleroderma/morphea: a scoping literature review.Pediatr Rheumatol Online J. 2024 Aug 21;22(1):77. doi: 10.1186/s12969-024-01014-x. Pediatr Rheumatol Online J. 2024. PMID: 39169409 Free PMC article.
-
Disease course and long-term outcome of juvenile localized scleroderma: Experience from a single pediatric rheumatology Centre and literature review.Autoimmun Rev. 2018 Jul;17(7):727-734. doi: 10.1016/j.autrev.2018.02.004. Epub 2018 May 3. Autoimmun Rev. 2018. PMID: 29729451 Review.
Cited by
-
The Serological Evidence of Positive Rheumatoid Factor in Morphea Patients and Its Relation to Disease Severity.Cureus. 2024 May 26;16(5):e61105. doi: 10.7759/cureus.61105. eCollection 2024 May. Cureus. 2024. PMID: 38919251 Free PMC article.
-
Radiation-induced morphea of the breast - characterization and treatment of fibroblast dysfunction with repurposed mesalazine.Sci Rep. 2024 Oct 30;14(1):26132. doi: 10.1038/s41598-024-74206-w. Sci Rep. 2024. PMID: 39477958 Free PMC article.
-
Damage evaluation of craniofacial localized scleroderma using magnetic resonance imaging.Quant Imaging Med Surg. 2024 Feb 1;14(2):1891-1903. doi: 10.21037/qims-23-980. Epub 2024 Jan 19. Quant Imaging Med Surg. 2024. PMID: 38415131 Free PMC article.
-
Consensus-based recommendations for the management of juvenile localised scleroderma.Ann Rheum Dis. 2019 Aug;78(8):1019-1024. doi: 10.1136/annrheumdis-2018-214697. Epub 2019 Mar 2. Ann Rheum Dis. 2019. PMID: 30826775 Free PMC article.
-
Interferon-Gamma-Inducible Protein-10 (IP-10) and Tumor Necrosis Factor-α (TNF-α) as Serological Predictors of Active Disease Status in Localized Scleroderma.Int J Mol Sci. 2024 Sep 21;25(18):10134. doi: 10.3390/ijms251810134. Int J Mol Sci. 2024. PMID: 39337619 Free PMC article.
References
-
- Peterson LS, Nelson AM, Su WP, Mason T, O'Fallon WM, Gabriel SE. The epidemiology of morphea (localized scleroderma) in Olmsted County 1960–1993. J Rheumatol. 1997;24:73–80. PubMed PMID: 9002014. - PubMed
-
- Fett N, Werth VP. Update on morphea: part I. Epidemiology, clinical presentation, and pathogenesis. J Am Acad Dermatol. 2011;64:217–228. quiz 29-30. PubMed PMID: 21238823. - PubMed
-
- Zulian F, Vallongo C, Woo P, Russo R, Ruperto N, Harper J, et al. Localized scleroderma in childhood is not just a skin disease. Arthritis Rheum. 2005;52:2873–2881. PubMed PMID: 16142730. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical