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Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images

BACKGROUND: Reflectance confocal microscopy (RCM) allows for real‐time in vivo visualization of the epidermis at the cellular level noninvasively. Parameters relating to tissue architecture can be extracted from RCM images, however, analysis of such images requires manual identification of cells to...

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Autores principales: Lboukili, Imane, Stamatas, Georgios N., Descombes, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177282/
https://www.ncbi.nlm.nih.gov/pubmed/37231922
http://dx.doi.org/10.1111/srt.13343
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author Lboukili, Imane
Stamatas, Georgios N.
Descombes, Xavier
author_facet Lboukili, Imane
Stamatas, Georgios N.
Descombes, Xavier
author_sort Lboukili, Imane
collection PubMed
description BACKGROUND: Reflectance confocal microscopy (RCM) allows for real‐time in vivo visualization of the epidermis at the cellular level noninvasively. Parameters relating to tissue architecture can be extracted from RCM images, however, analysis of such images requires manual identification of cells to derive these parameters, which can be time‐consuming and subject to human error, highlighting the need for an automated cell identification method. METHODS: First, the region‐of‐interest (ROI) containing cells needs to be identified, followed by the identification of individual cells within the ROI. To perform this task, we use successive applications of Sato and Gabor filters. The final step is post‐processing improvement of cell detection and removal of size outliers. The proposed algorithm is evaluated on manually annotated real data. It is then applied to 5345 images to study the evolution of epidermal architecture in children and adults. The images were acquired on the volar forearm of healthy children (3 months to 10 years) and women (25–80 years), and on the volar forearm and cheek of women (40–80 years). Following the identification of cell locations, parameters such as cell area, cell perimeter, and cell density are calculated, as well as the probability distribution of the number of nearest neighbors per cell. The thicknesses of the Stratum Corneum and supra‐papillary epidermis are also calculated using a hybrid deep‐learning method. RESULTS: Epidermal keratinocytes are significantly larger (area and perimeter) in the granular layer than in the spinous layer and they get progressively larger with a child's age. Skin continues to mature dynamically during adulthood, as keratinocyte size continues to increase with age on both the cheeks and volar forearm, but the topology and cell aspect ratio remain unchanged across different epidermal layers, body sites, and age. Stratum Corneum and supra‐papillary epidermis thicknesses increase with age, at a faster rate in children than in adults. CONCLUSIONS: The proposed methodology can be applied to large datasets to automate image analysis and the calculation of parameters relevant to skin physiology. These data validate the dynamic nature of skin maturation during childhood and skin aging in adulthood.
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spelling pubmed-101772822023-08-11 Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images Lboukili, Imane Stamatas, Georgios N. Descombes, Xavier Skin Res Technol Original Articles BACKGROUND: Reflectance confocal microscopy (RCM) allows for real‐time in vivo visualization of the epidermis at the cellular level noninvasively. Parameters relating to tissue architecture can be extracted from RCM images, however, analysis of such images requires manual identification of cells to derive these parameters, which can be time‐consuming and subject to human error, highlighting the need for an automated cell identification method. METHODS: First, the region‐of‐interest (ROI) containing cells needs to be identified, followed by the identification of individual cells within the ROI. To perform this task, we use successive applications of Sato and Gabor filters. The final step is post‐processing improvement of cell detection and removal of size outliers. The proposed algorithm is evaluated on manually annotated real data. It is then applied to 5345 images to study the evolution of epidermal architecture in children and adults. The images were acquired on the volar forearm of healthy children (3 months to 10 years) and women (25–80 years), and on the volar forearm and cheek of women (40–80 years). Following the identification of cell locations, parameters such as cell area, cell perimeter, and cell density are calculated, as well as the probability distribution of the number of nearest neighbors per cell. The thicknesses of the Stratum Corneum and supra‐papillary epidermis are also calculated using a hybrid deep‐learning method. RESULTS: Epidermal keratinocytes are significantly larger (area and perimeter) in the granular layer than in the spinous layer and they get progressively larger with a child's age. Skin continues to mature dynamically during adulthood, as keratinocyte size continues to increase with age on both the cheeks and volar forearm, but the topology and cell aspect ratio remain unchanged across different epidermal layers, body sites, and age. Stratum Corneum and supra‐papillary epidermis thicknesses increase with age, at a faster rate in children than in adults. CONCLUSIONS: The proposed methodology can be applied to large datasets to automate image analysis and the calculation of parameters relevant to skin physiology. These data validate the dynamic nature of skin maturation during childhood and skin aging in adulthood. John Wiley and Sons Inc. 2023-05-12 /pmc/articles/PMC10177282/ /pubmed/37231922 http://dx.doi.org/10.1111/srt.13343 Text en © 2023 The Authors. Skin Research and Technology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Lboukili, Imane
Stamatas, Georgios N.
Descombes, Xavier
Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
title Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
title_full Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
title_fullStr Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
title_full_unstemmed Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
title_short Age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
title_sort age‐dependent changes in epidermal architecture explored using an automated image analysis algorithm on in vivo reflectance confocal microscopy images
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177282/
https://www.ncbi.nlm.nih.gov/pubmed/37231922
http://dx.doi.org/10.1111/srt.13343
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