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Ultrastructural changes induced in cutaneous collagen by ultraviolet‐A1 and psoralen plus ultraviolet A therapy in systemic sclerosis
Author(s) -
SAKAKIBARA Noriyuki,
SUGANO Shigeru,
MORITA Akimichi
Publication year - 2008
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/j.1346-8138.2008.00417.x
Subject(s) - psoralen , fibril , puva therapy , dermis , collagen fibril , reticular connective tissue , ultrastructure , pathology , chemistry , ultraviolet a , type i collagen , biophysics , anatomy , medicine , dermatology , psoriasis , biology , biochemistry , dna
In the present study, we examined the ultrastructural alterations in collagen fibrils clinically softened by ultraviolet‐A1 (UVA1, 340–400 nm) therapy and psoralen plus long‐wave ultraviolet (PUVA) therapy and compared collagen fibril diameters in four patients with systemic sclerosis (SSc). In skin sclerosis, the dermis is compacted from the epidermal layer to the sweat glands, and the collagen bundles are thicker with decreased space between them. We obtained skin specimens before and after UVA1 or PUVA therapy, and compared cutaneous alterations in one diffuse‐type patient and one limited‐type patient following UVA1 therapy, and in two diffuse‐type patients following PUVA treatment. Ultramicroscopic analysis revealed that UVA1 treatment decreased the diameter of the broad collagen fibrils, mainly in the upper reticular layer. PUVA induced similar alterations in the collagen fibrils, extending to the upper and middle reticular layers. PUVA therapy induced alterations in collagen fibril diameter in deeper layers than did UVA1 therapy, which might be related to the direct action of UV light and the depth of the light penetration. In three of four patients, collagen fibril diameter decreased, collagen fibril thickness equalized, and new, thin fibrils developed among the collagen fibrils, suggesting that collagen degradation and synthesis underlie the alterations induced by UVA1 and PUVA phototherapies.