In vivo endoscopic Doppler optical coherence tomography imaging of the colon

Background and ObjectiveColorectal cancer (CRC) remains the second deadliest cancer in the United States. Several screening methods exist; however, detection of small polyps remains a challenge. Optical coherence tomography (OCT) has been demonstrated to be capable of detecting lesions as small as 1...

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Main Authors: Welge, Weston A., Barton, Jennifer K.
Other Authors: College of Optical Sciences, The University of Arizona
Language:en
Published: WILEY 2017
Subjects:
Online Access:http://hdl.handle.net/10150/623988
http://arizona.openrepository.com/arizona/handle/10150/623988
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spelling ndltd-arizona.edu-oai-arizona.openrepository.com-10150-6239882017-06-08T03:00:32Z In vivo endoscopic Doppler optical coherence tomography imaging of the colon Welge, Weston A. Barton, Jennifer K. College of Optical Sciences, The University of Arizona Department of Biomedical Engineering, The University of Arizona College of Optical Sciences; The University of Arizona; Tucson 85721 Arizona College of Optical Sciences; The University of Arizona; Tucson 85721 Arizona colorectal cancer adenoma image processing vascular imaging Background and ObjectiveColorectal cancer (CRC) remains the second deadliest cancer in the United States. Several screening methods exist; however, detection of small polyps remains a challenge. Optical coherence tomography (OCT) has been demonstrated to be capable of detecting lesions as small as 1mm in the mouse colon, but detection is based on measuring a doubling of the mucosa thickness. The colon microvasculature may be an attractive biomarker of early tumor development because tumor vessels are characterized by irregular structure and dysfunction. Our goal was to develop an endoscopic method of detecting and segmenting colon vessels using Doppler OCT to enable future studies for improving early detection and development of novel chemopreventive agents. MethodWe conducted in vivo colon imaging in an azoxymethane (AOM)-treated mouse model of colorectal cancer using a miniature endoscope and a swept-source OCT system at 1,040nm with a 16kHz sweep rate. We applied the Kasai autocorrelation algorithm to laterally oversampled OCT B-scans to resolve vascular flow in the mucosa and submucosa. Vessels were segmented by applying a series of image processing steps: (i) intensity thresholding; (ii) two-dimensional matched filtering; and (iii) histogram segmentation. ResultsWe observed differences in the vessels sizes and spatial distribution in a mature adenoma compared to surrounding undiseased tissue and compared the results with histology. We also imaged flow in four young mice (two AOM-treated and two control) showing no significant differences, which is expected so early after carcinogen exposure. We also present flow images of adenoma in a living mouse and a euthanized mouse to demonstrate that no flow is detected after euthanasia. ConclusionWe present, to the best of our knowledge, the first Doppler OCT images of in vivo mouse colon collected with a fiber-based endoscope. We also describe a fast and robust image processing method for segmenting vessels in the colon. These results suggest that Doppler OCT is a promising imaging modality for vascular imaging in the colon that requires no exogenous contrast agents. 2017-03 Article In vivo endoscopic Doppler optical coherence tomography imaging of the colon 2017, 49 (3):249 Lasers in Surgery and Medicine 01968092 10.1002/lsm.22578 http://hdl.handle.net/10150/623988 http://arizona.openrepository.com/arizona/handle/10150/623988 Lasers in Surgery and Medicine en http://doi.wiley.com/10.1002/lsm.22578 © 2016 Wiley Periodicals, Inc. WILEY
collection NDLTD
language en
sources NDLTD
topic colorectal cancer
adenoma
image processing
vascular imaging
spellingShingle colorectal cancer
adenoma
image processing
vascular imaging
Welge, Weston A.
Barton, Jennifer K.
In vivo endoscopic Doppler optical coherence tomography imaging of the colon
description Background and ObjectiveColorectal cancer (CRC) remains the second deadliest cancer in the United States. Several screening methods exist; however, detection of small polyps remains a challenge. Optical coherence tomography (OCT) has been demonstrated to be capable of detecting lesions as small as 1mm in the mouse colon, but detection is based on measuring a doubling of the mucosa thickness. The colon microvasculature may be an attractive biomarker of early tumor development because tumor vessels are characterized by irregular structure and dysfunction. Our goal was to develop an endoscopic method of detecting and segmenting colon vessels using Doppler OCT to enable future studies for improving early detection and development of novel chemopreventive agents. MethodWe conducted in vivo colon imaging in an azoxymethane (AOM)-treated mouse model of colorectal cancer using a miniature endoscope and a swept-source OCT system at 1,040nm with a 16kHz sweep rate. We applied the Kasai autocorrelation algorithm to laterally oversampled OCT B-scans to resolve vascular flow in the mucosa and submucosa. Vessels were segmented by applying a series of image processing steps: (i) intensity thresholding; (ii) two-dimensional matched filtering; and (iii) histogram segmentation. ResultsWe observed differences in the vessels sizes and spatial distribution in a mature adenoma compared to surrounding undiseased tissue and compared the results with histology. We also imaged flow in four young mice (two AOM-treated and two control) showing no significant differences, which is expected so early after carcinogen exposure. We also present flow images of adenoma in a living mouse and a euthanized mouse to demonstrate that no flow is detected after euthanasia. ConclusionWe present, to the best of our knowledge, the first Doppler OCT images of in vivo mouse colon collected with a fiber-based endoscope. We also describe a fast and robust image processing method for segmenting vessels in the colon. These results suggest that Doppler OCT is a promising imaging modality for vascular imaging in the colon that requires no exogenous contrast agents.
author2 College of Optical Sciences, The University of Arizona
author_facet College of Optical Sciences, The University of Arizona
Welge, Weston A.
Barton, Jennifer K.
author Welge, Weston A.
Barton, Jennifer K.
author_sort Welge, Weston A.
title In vivo endoscopic Doppler optical coherence tomography imaging of the colon
title_short In vivo endoscopic Doppler optical coherence tomography imaging of the colon
title_full In vivo endoscopic Doppler optical coherence tomography imaging of the colon
title_fullStr In vivo endoscopic Doppler optical coherence tomography imaging of the colon
title_full_unstemmed In vivo endoscopic Doppler optical coherence tomography imaging of the colon
title_sort in vivo endoscopic doppler optical coherence tomography imaging of the colon
publisher WILEY
publishDate 2017
url http://hdl.handle.net/10150/623988
http://arizona.openrepository.com/arizona/handle/10150/623988
work_keys_str_mv AT welgewestona invivoendoscopicdoppleropticalcoherencetomographyimagingofthecolon
AT bartonjenniferk invivoendoscopicdoppleropticalcoherencetomographyimagingofthecolon
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