Observations of dystrophic epidermolysis bullosa patients with collagen VII NC2 truncation provide new insights into anchoring fibril assembly
3 March 2026Characterisation of the wound microbiome and antimicrobial resistance profiles in clinical isolates from epidermolysis bullosa patients
7 March 2026Br J Dermatol. 2026 Mar 5:ljag082. doi: 10.1093/bjd/ljag082. Epub ahead of print. PMID: 41787717
Systemic inflammation in recessive dystrophic epidermolysis bullosa: a five-year longitudinal study
Authors: Karakioulaki M, Yang H, Hess M, Binder H, Eyerich K, Has C.
Affiliation:
- Department of Dermatology and Venereology, Faculty of Medicine and Medical Center, University Hospital Freiburg, Germany.
- Institute of Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, Germany.
Abstract:
Background: Recessive dystrophic epidermolysis bullosa (RDEB) is characterized by skin fragility, extensive wounding, and systemic complications. While inflammation contributes to disease severity, its pattern, longitudinal dynamics and clinical correlates remain poorly defined.
Objective: To characterize the course of systemic inflammatory markers over time in patients with RDEB and explore their associations with clinical, microbiological, and laboratory parameters.
Methods: This retrospective longitudinal study analyzed clinical and laboratory data of 120 visits within 5 years from 44 patients with intermediate (N=22) and severe (N=22) RDEB. Acute-phase proteins (CRP, IL-6, SAA), neutrophil to lymphocyte ratio (NLR), leukocytes, thrombocytes and ferritin were examined in relation to wound body surface area, mucosal involvement, collagen VII (C7) protein expression levels, squamous cell carcinoma (SCC) presence, nutritional status, anemia markers, wound microbiology and immunoglobulins.
Results: Severe RDEB showed an early and sustained systemic inflammatory profile, with CRP, IL-6, and SAA elevated >3.5-fold from early childhood, plateauing in mid-adulthood. Intermediate RDEB maintained low inflammatory activity throughout life. Acute phase proteins and NLR were significantly elevated in the presence of SCC (CRP: p<0.001; IL-6: p=0.002; SAA: p=0.011; NLR: p=0.004), collagen VII absence (CRP: p=0.002), and colonization by Pseudomonas (CRP, IL-6: p<0.001) or fungi (CRP: p=0.006). CRP and age were the most robust independent predictors of SCC risk. Streptococcus, Pseudomonas, fungi, or polymicrobial colonization were associated with a broader systemic inflammatory response, when compared to infections with Staphylococcus. Hypoalbuminemia and elevated immunoglobulins correlated with inflammatory markers and anemia of chronic disease was reflected by declining iron and increased ferritin levels. In multivariable models, reduced C7 expression, wound burden and SCC were the strongest independent predictors of acute phase inflammation.
Conclusions: This study reveals that severe RDEB involves early-onset, progressive systemic inflammation that peaks in mid-adulthood and then plateaus, suggesting a critical window for therapeutic intervention. In contrast, intermediate RDEB shows minimal systemic inflammation. The findings support a three-tiered treatment approach-wound burden reduction through curative/corrective interventions, antimicrobial strategies and anti-inflammatory therapy -aligned with standard of care and nutritional supplementation.