Correlating Optical Coherence Tomography and Other Noninvasive Imaging Features With Atrophic and Hypertrophic Skin Photoaging
ABSTRACT Background According to morphological and clinical differences, atrophic (AP) and hypertrophic (HP) skin photoaging types have been reported. The current study examines the correlation between optical coherence tomography (OCT) and dynamic‐OCT (D‐OCT) features in subjects with skin photoagi...
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Published in | International journal of dermatology Vol. 64; no. 8; pp. 1441 - 1445 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.08.2025
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | ABSTRACT
Background
According to morphological and clinical differences, atrophic (AP) and hypertrophic (HP) skin photoaging types have been reported. The current study examines the correlation between optical coherence tomography (OCT) and dynamic‐OCT (D‐OCT) features in subjects with skin photoaging types classified as AP, HP, or controls. Furthermore, we aim to define the correlations between OCT/D‐OCT and other noninvasive skin imaging features (standardized clinical photography and reflectance confocal microscopy [RCM]).
Methods
We explored the correlations between skin photoaging types, OCT/D‐OCT, and noninvasive skin imaging features. A total of 58 patients were clinically classified as AP (n = 17), HP (n = 24), or controls (n = 17).
Results
AP subjects showed higher D‐OCT vessel assets and vessel densities (p < 0.05) compared to HP and control subjects. A significant correlation was established between standardized clinical evidence of wrinkles and RCM collagen scores. Dermal variations in HP subjects represent the underlying substrate of wrinkles.
Conclusions
Despite the limited cohort, these results contribute to the current knowledge of morphologic differences between AP and HP subjects. Treatment should consider morphologic changes according to skin photoaging phenotypes for optimal personalized medicine. |
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Bibliography: | The authors received no specific funding for this work. Funding ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Funding: The authors received no specific funding for this work. |
ISSN: | 0011-9059 1365-4632 1365-4632 |
DOI: | 10.1111/ijd.17799 |