Cargando…

Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning

The autoimmune disease systemic sclerosis (SSc) causes microvascular changes that can be easily observed cutaneously at the finger nailfold. Optoacoustic imaging (OAI), a combination of optical and ultrasound imaging, specifically raster-scanning optoacoustic mesoscopy (RSOM), offers a non-invasive...

Descripción completa

Detalles Bibliográficos
Autores principales: Nitkunanantharajah, Suhanyaa, Haedicke, Katja, Moore, Tonia B., Manning, Joanne B., Dinsdale, Graham, Berks, Michael, Taylor, Christopher, Dickinson, Mark R., Jüstel, Dominik, Ntziachristos, Vasilis, Herrick, Ariane L., Murray, Andrea K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536218/
https://www.ncbi.nlm.nih.gov/pubmed/33020505
http://dx.doi.org/10.1038/s41598-020-73319-2
_version_ 1783590518095085568
author Nitkunanantharajah, Suhanyaa
Haedicke, Katja
Moore, Tonia B.
Manning, Joanne B.
Dinsdale, Graham
Berks, Michael
Taylor, Christopher
Dickinson, Mark R.
Jüstel, Dominik
Ntziachristos, Vasilis
Herrick, Ariane L.
Murray, Andrea K.
author_facet Nitkunanantharajah, Suhanyaa
Haedicke, Katja
Moore, Tonia B.
Manning, Joanne B.
Dinsdale, Graham
Berks, Michael
Taylor, Christopher
Dickinson, Mark R.
Jüstel, Dominik
Ntziachristos, Vasilis
Herrick, Ariane L.
Murray, Andrea K.
author_sort Nitkunanantharajah, Suhanyaa
collection PubMed
description The autoimmune disease systemic sclerosis (SSc) causes microvascular changes that can be easily observed cutaneously at the finger nailfold. Optoacoustic imaging (OAI), a combination of optical and ultrasound imaging, specifically raster-scanning optoacoustic mesoscopy (RSOM), offers a non-invasive high-resolution 3D visualization of capillaries allowing for a better view of microvascular changes and an extraction of volumetric measures. In this study, nailfold capillaries of patients with SSc and healthy controls are imaged and compared with each other for the first time using OAI. The nailfolds of 23 patients with SSc and 19 controls were imaged using RSOM. The acquired images were qualitatively compared to images from state-of-the-art imaging tools for SSc, dermoscopy and high magnification capillaroscopy. The vascular volume in the nailfold capillaries were computed from the RSOM images. The vascular volumes differ significantly between both cohorts (0.216 ± 0.085 mm(3) and 0.337 ± 0.110 mm(3); p < 0.0005). In addition, an artificial neural network was trained to automatically differentiate nailfold images from both cohorts to further assess whether OAI is sensitive enough to visualize anatomical differences in the capillaries between the two cohorts. Using transfer learning, the model classifies images with an area under the ROC curve of 0.897, and a sensitivity of 0.783 and specificity of 0.895. In conclusion, this study demonstrates the capabilities of RSOM as an imaging tool for SSc and establishes it as a modality that facilitates more in-depth studies into the disease mechanisms and progression.
format Online
Article
Text
id pubmed-7536218
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75362182020-10-07 Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning Nitkunanantharajah, Suhanyaa Haedicke, Katja Moore, Tonia B. Manning, Joanne B. Dinsdale, Graham Berks, Michael Taylor, Christopher Dickinson, Mark R. Jüstel, Dominik Ntziachristos, Vasilis Herrick, Ariane L. Murray, Andrea K. Sci Rep Article The autoimmune disease systemic sclerosis (SSc) causes microvascular changes that can be easily observed cutaneously at the finger nailfold. Optoacoustic imaging (OAI), a combination of optical and ultrasound imaging, specifically raster-scanning optoacoustic mesoscopy (RSOM), offers a non-invasive high-resolution 3D visualization of capillaries allowing for a better view of microvascular changes and an extraction of volumetric measures. In this study, nailfold capillaries of patients with SSc and healthy controls are imaged and compared with each other for the first time using OAI. The nailfolds of 23 patients with SSc and 19 controls were imaged using RSOM. The acquired images were qualitatively compared to images from state-of-the-art imaging tools for SSc, dermoscopy and high magnification capillaroscopy. The vascular volume in the nailfold capillaries were computed from the RSOM images. The vascular volumes differ significantly between both cohorts (0.216 ± 0.085 mm(3) and 0.337 ± 0.110 mm(3); p < 0.0005). In addition, an artificial neural network was trained to automatically differentiate nailfold images from both cohorts to further assess whether OAI is sensitive enough to visualize anatomical differences in the capillaries between the two cohorts. Using transfer learning, the model classifies images with an area under the ROC curve of 0.897, and a sensitivity of 0.783 and specificity of 0.895. In conclusion, this study demonstrates the capabilities of RSOM as an imaging tool for SSc and establishes it as a modality that facilitates more in-depth studies into the disease mechanisms and progression. Nature Publishing Group UK 2020-10-05 /pmc/articles/PMC7536218/ /pubmed/33020505 http://dx.doi.org/10.1038/s41598-020-73319-2 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nitkunanantharajah, Suhanyaa
Haedicke, Katja
Moore, Tonia B.
Manning, Joanne B.
Dinsdale, Graham
Berks, Michael
Taylor, Christopher
Dickinson, Mark R.
Jüstel, Dominik
Ntziachristos, Vasilis
Herrick, Ariane L.
Murray, Andrea K.
Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
title Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
title_full Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
title_fullStr Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
title_full_unstemmed Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
title_short Three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
title_sort three-dimensional optoacoustic imaging of nailfold capillaries in systemic sclerosis and its potential for disease differentiation using deep learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536218/
https://www.ncbi.nlm.nih.gov/pubmed/33020505
http://dx.doi.org/10.1038/s41598-020-73319-2
work_keys_str_mv AT nitkunanantharajahsuhanyaa threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT haedickekatja threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT mooretoniab threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT manningjoanneb threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT dinsdalegraham threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT berksmichael threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT taylorchristopher threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT dickinsonmarkr threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT justeldominik threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT ntziachristosvasilis threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT herrickarianel threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning
AT murrayandreak threedimensionaloptoacousticimagingofnailfoldcapillariesinsystemicsclerosisanditspotentialfordiseasedifferentiationusingdeeplearning