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Characterization of clinical photosensitivity in cutaneous lupus erythematosus
Background Photosensitivity (PS) in lupus erythematosus (LE) is frequently determined by patient report. Objective We sought to characterize self-reported PS in cutaneous LE (CLE). Methods The PS survey was used to classify subject responses into 5 phenotypes: direct sun-induced CLE flare (directCLE...
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Published in: | Journal of the American Academy of Dermatology 2013-08, Vol.69 (2), p.205-213 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background Photosensitivity (PS) in lupus erythematosus (LE) is frequently determined by patient report. Objective We sought to characterize self-reported PS in cutaneous LE (CLE). Methods The PS survey was used to classify subject responses into 5 phenotypes: direct sun-induced CLE flare (directCLE); general exacerbation of CLE (genCLE); polymorphic light eruption–like reactions (genSkin); general pruritus/paresthesias (genRxn); and sun-induced systemic symptoms (genSys). In all, 91 subjects with CLE alone or with CLE and systemic LE were interviewed. Results In all, 81% ascribed to 1 or more PS phenotypes. CLE-specific reactions (direct sun-induced CLE flare or general exacerbation of CLE) were reported by 86% of photosensitive subjects. Higher CLE disease activity (measured by CLE Disease Area and Severity Index activity scores) was suggestive of direct sun-induced CLE flare reactions ( P = .09). In all, 60% of photosensitive subjects described CLE-nonspecific reactions: polymorphic light eruption–like rash and general pruritus/paresthesias. These phenotypes often co-occurred with CLE-specific reactions and were predicted by more systemic disease activity as measured by Physicians Global Assessment (PGA) scores in regression analyses (genSkin, P = .02) and (genRxn, P = .05). In all, 36% of subjects reported systemic reactions and higher PGA scores were predictive of the sun-induced systemic symptoms phenotype ( P = .02); a diagnosis of systemic LE was not ( P = .14). Limitations PS was inferred from patient report and not directly observed. Conclusions Characterization of self-reported PS in LE reveals that patients experience combinations of CLE-specific, CLE-nonspecific, and systemic reactions to sunlight. Sun-induced CLE flares are associated with more active CLE disease. Polymorphic light eruption–like, generalized pruritus/paresthesias, and systemic reactions are associated with more active systemic disease. Recognition of PS phenotypes will permit improved definitions of clinical PS and allow for more precise investigation into its pathophysiology. |
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ISSN: | 0190-9622 1097-6787 |
DOI: | 10.1016/j.jaad.2013.03.015 |