Measuring Skin Fibrosis in Systemic Sclerosis - EMJ

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A Non-Invasive Way to Measure Skin Fibrosis in Systemic Sclerosis

Key Summary:

  • This prospective cohort study evaluated SFDI in 49 patients with systemic sclerosis and 25 controls.
  • Each one-point mRSS rise was linked to lower Rd (β: −0.0028; p=0.014).
  • The authors supported SFDI as a quantitative skin fibrosis outcome measure in systemic sclerosis.

SPATIAL frequency domain imaging (SFDI), a non-contact optical method, has emerged as a potential objective measure of skin fibrosis in systemic sclerosis, according to a new prospective cohort study.

Skin Fibrosis and Measurement Gaps

Systemic sclerosis is an autoimmune disease with no approved skin-directed therapies, and the modified Rodnan skin score (mRSS), the standard measure of skin involvement, has limitations. A non-invasive, objective and scalable measure of skin fibrosis in systemic sclerosis suitable for multicentre trials was lacking.

Prospective Single-Centre Cohort Design

This single-centre, prospective cohort study was conducted at Boston Medical Center (Boston, MA, USA). Between October 2019 and June 2025, 54 patients with systemic sclerosis and 30 controls without autoimmune disease were enrolled; 49 and 25 respectively were analysed, with biopsies from 34 and 16.

Among those analysed, 78% of patients and 80% of controls were female, and mean age was 50 and 49 years respectively. Assessments included SFDI, mRSS and optional forearm biopsy, with follow-up every 3 months in year one and every 6 months thereafter for 3 years in the expanded phase.

Main analyses assessed baseline associations of diffuse reflectance (Rd) and reduced scattering coefficient (μs′) with mRSS, and correlations with histological dermal fibrosis.

SFDI Parameters and Histological Fibrosis

Rd and μs′ were significantly lower in patients with systemic sclerosis than in controls across all mRSS strata, including sites where mRSS was 0.

Each one-point increase in local mRSS was associated with decreases in Rd (β: −0.0028; 95% confidence interval [CI]: −0.0050 to −0.0006; p=0.014) and μs′ (β: −0.0158; 95% CI: −0.0314 to −0.0003; p=0.047).

SFDI correlations were weak to moderate with mRSS (r: −0.48 to −0.38) and moderate with histological fibrosis (r: −0.52 to −0.34).

Quantitative Outcome Measure Potential

These findings have suggested that SFDI provides an objective, non-invasive measure of skin involvement that aligns with established assessments, supporting its potential as a quantitative outcome measure for evaluating skin disease, consistent with Outcome Measures in Rheumatology principles.

Reference

Vo H et al. Spatial frequency domain imaging for assessment of skin fibrosis in systemic sclerosis: a prospective cohort study. Lancet Rheumatol. 2026;DOI:10.1016/S2665-9913(26)00229-8

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