A simple and robust method for automating analysis of naïve and regenerating peripheral nerves
Manual axon histomorphometry (AH) is time- and resource-intensive, which has inspired many attempts at automation. However, there has been little investigation on implementation of automated programs for widespread use. Ideally such a program should be able to perform AH across imaging modalities an...
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description | Manual axon histomorphometry (AH) is time- and resource-intensive, which has inspired many attempts at automation. However, there has been little investigation on implementation of automated programs for widespread use. Ideally such a program should be able to perform AH across imaging modalities and nerve states. AxonDeepSeg (ADS) is an open source deep learning program that has previously been validated in electron microscopy. We evaluated the robustness of ADS for peripheral nerve axonal histomorphometry in light micrographs prepared using two different methods.
Axon histomorphometry using ADS and manual analysis (gold-standard) was performed on light micrographs of naïve or regenerating rat median nerve cross-sections prepared with either toluidine-resin or osmium-paraffin embedding protocols. The parameters of interest included axon count, axon diameter, myelin thickness, and g-ratio.
Manual and automatic ADS axon counts demonstrated good agreement in naïve nerves and moderate agreement on regenerating nerves. There were small but consistent differences in measured axon diameter, myelin thickness and g-ratio; however, absolute differences were small. Both methods appropriately identified differences between naïve and regenerating nerves. ADS was faster than manual axon analysis.
Without any algorithm retraining, ADS was able to appropriately identify critical differences between naïve and regenerating nerves and work with different sample preparation methods of peripheral nerve light micrographs. While there were differences between absolute values between manual and ADS, ADS performed consistently and required much less time. ADS is an accessible and robust tool for AH that can provide consistent analysis across protocols and nerve states. |
doi_str_mv | 10.1371/journal.pone.0248323 |
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Axon histomorphometry using ADS and manual analysis (gold-standard) was performed on light micrographs of naïve or regenerating rat median nerve cross-sections prepared with either toluidine-resin or osmium-paraffin embedding protocols. The parameters of interest included axon count, axon diameter, myelin thickness, and g-ratio.
Manual and automatic ADS axon counts demonstrated good agreement in naïve nerves and moderate agreement on regenerating nerves. There were small but consistent differences in measured axon diameter, myelin thickness and g-ratio; however, absolute differences were small. Both methods appropriately identified differences between naïve and regenerating nerves. ADS was faster than manual axon analysis.
Without any algorithm retraining, ADS was able to appropriately identify critical differences between naïve and regenerating nerves and work with different sample preparation methods of peripheral nerve light micrographs. While there were differences between absolute values between manual and ADS, ADS performed consistently and required much less time. ADS is an accessible and robust tool for AH that can provide consistent analysis across protocols and nerve states.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0248323</identifier><identifier>PMID: 34234376</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Algorithms ; Analysis ; Animals ; Automation ; Axons ; Axons - physiology ; Biology and Life Sciences ; Biomedical engineering ; Computer and Information Sciences ; Deep Learning ; Diameters ; Electron microscopy ; Embedding ; Histomorphometry ; Image Processing, Computer-Assisted - methods ; Laboratory animals ; Learning programs ; Machine learning ; Male ; Mechanization ; Median nerve ; Median Nerve - physiology ; Medicine and Health Sciences ; Methods ; Micrography ; Microscopy ; Myelin ; Myelin Sheath - physiology ; Nerve Regeneration - physiology ; Nervous system ; Osmium ; Paraffin ; Paraffins ; Peripheral nerves ; Peripheral Nerves - physiology ; Photomicrographs ; Physical Sciences ; Rats ; Reconstructive surgery ; Research and Analysis Methods ; Robustness ; Sample preparation ; Thickness ; Toluidine</subject><ispartof>PloS one, 2021-07, Vol.16 (7), p.e0248323</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Wong et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Wong et al 2021 Wong et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-e9641b973338f23e4db53d710c451ae9949141247a53e84c69ff78df1a6112233</citedby><cites>FETCH-LOGICAL-c692t-e9641b973338f23e4db53d710c451ae9949141247a53e84c69ff78df1a6112233</cites><orcidid>0000-0003-3662-9532 ; 0000-0002-9697-9799 ; 0000-0003-4156-5748 ; 0000-0003-0414-0556 ; 0000-0002-9819-221X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263263/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263263/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34234376$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Cymbalyuk, Gennady S.</contributor><creatorcontrib>Wong, Alison L</creatorcontrib><creatorcontrib>Hricz, Nicholas</creatorcontrib><creatorcontrib>Malapati, Harsha</creatorcontrib><creatorcontrib>von Guionneau, Nicholas</creatorcontrib><creatorcontrib>Wong, Michael</creatorcontrib><creatorcontrib>Harris, Thomas</creatorcontrib><creatorcontrib>Boudreau, Mathieu</creatorcontrib><creatorcontrib>Cohen-Adad, Julien</creatorcontrib><creatorcontrib>Tuffaha, Sami</creatorcontrib><title>A simple and robust method for automating analysis of naïve and regenerating peripheral nerves</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Manual axon histomorphometry (AH) is time- and resource-intensive, which has inspired many attempts at automation. However, there has been little investigation on implementation of automated programs for widespread use. Ideally such a program should be able to perform AH across imaging modalities and nerve states. AxonDeepSeg (ADS) is an open source deep learning program that has previously been validated in electron microscopy. We evaluated the robustness of ADS for peripheral nerve axonal histomorphometry in light micrographs prepared using two different methods.
Axon histomorphometry using ADS and manual analysis (gold-standard) was performed on light micrographs of naïve or regenerating rat median nerve cross-sections prepared with either toluidine-resin or osmium-paraffin embedding protocols. The parameters of interest included axon count, axon diameter, myelin thickness, and g-ratio.
Manual and automatic ADS axon counts demonstrated good agreement in naïve nerves and moderate agreement on regenerating nerves. There were small but consistent differences in measured axon diameter, myelin thickness and g-ratio; however, absolute differences were small. Both methods appropriately identified differences between naïve and regenerating nerves. ADS was faster than manual axon analysis.
Without any algorithm retraining, ADS was able to appropriately identify critical differences between naïve and regenerating nerves and work with different sample preparation methods of peripheral nerve light micrographs. While there were differences between absolute values between manual and ADS, ADS performed consistently and required much less time. ADS is an accessible and robust tool for AH that can provide consistent analysis across protocols and nerve states.</description><subject>Algorithms</subject><subject>Analysis</subject><subject>Animals</subject><subject>Automation</subject><subject>Axons</subject><subject>Axons - physiology</subject><subject>Biology and Life Sciences</subject><subject>Biomedical engineering</subject><subject>Computer and Information Sciences</subject><subject>Deep Learning</subject><subject>Diameters</subject><subject>Electron microscopy</subject><subject>Embedding</subject><subject>Histomorphometry</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Laboratory animals</subject><subject>Learning programs</subject><subject>Machine learning</subject><subject>Male</subject><subject>Mechanization</subject><subject>Median nerve</subject><subject>Median Nerve - physiology</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Micrography</subject><subject>Microscopy</subject><subject>Myelin</subject><subject>Myelin Sheath - physiology</subject><subject>Nerve Regeneration - physiology</subject><subject>Nervous system</subject><subject>Osmium</subject><subject>Paraffin</subject><subject>Paraffins</subject><subject>Peripheral nerves</subject><subject>Peripheral Nerves - physiology</subject><subject>Photomicrographs</subject><subject>Physical Sciences</subject><subject>Rats</subject><subject>Reconstructive surgery</subject><subject>Research and Analysis Methods</subject><subject>Robustness</subject><subject>Sample preparation</subject><subject>Thickness</subject><subject>Toluidine</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk1uL1DAUx4so7kW_gWhBEH2Ysbk0TV6EYfEysLDg7TWk7UknQ9t0k3RwP9V-CL-YGae7TGUfJIW0J7__Pz0nOUnyAmVLRAr0fmtH16t2OdgelhmmnGDyKDlFguAFwxl5fPR-kpx5v82ynHDGniYnhGJCScFOE7lKvemGFlLV16mz5ehD2kHY2DrV1qVqDLZTwfRNBFR7441PrU579ft2N2mggR7cgRnAmWETv9o0xnbgnyVPtGo9PJ_m8-THp4_fL74sLq8-ry9Wl4uKCRwWIBhFpSgIIVxjArQuc1IXKKtojhQIQQWiCNNC5QQ4jSKtC15rpBhCGBNynrw6-A6t9XKqjZc4j0IRK0AjsT4QtVVbOTjTKXcjrTLyb8C6RioXTNWCRACipGWNgCpaCVzmZVGSSgBWheZZFr0-TLuNZQd1BX2IKc9M5yu92cjG7iTHjMQnGrydDJy9HsEH2RlfQduqHux4-G_GORIioq__QR_ObqIaFRMwvbZx32pvKleMFQXBnLNILR-g4qihM1W8SNrE-EzwbiaITIBfoVGj93L97ev_s1c_5-ybI3YDqg0bb9sxGNv7OUgPYOWs9w70fZFRJvd9cFcNue8DOfVBlL08PqB70d3FJ38AFk0DTA</recordid><startdate>20210707</startdate><enddate>20210707</enddate><creator>Wong, Alison L</creator><creator>Hricz, Nicholas</creator><creator>Malapati, Harsha</creator><creator>von Guionneau, Nicholas</creator><creator>Wong, Michael</creator><creator>Harris, Thomas</creator><creator>Boudreau, Mathieu</creator><creator>Cohen-Adad, Julien</creator><creator>Tuffaha, Sami</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3662-9532</orcidid><orcidid>https://orcid.org/0000-0002-9697-9799</orcidid><orcidid>https://orcid.org/0000-0003-4156-5748</orcidid><orcidid>https://orcid.org/0000-0003-0414-0556</orcidid><orcidid>https://orcid.org/0000-0002-9819-221X</orcidid></search><sort><creationdate>20210707</creationdate><title>A simple and robust method for automating analysis of naïve and regenerating peripheral nerves</title><author>Wong, Alison L ; Hricz, Nicholas ; Malapati, Harsha ; von Guionneau, Nicholas ; Wong, Michael ; Harris, Thomas ; Boudreau, Mathieu ; Cohen-Adad, Julien ; Tuffaha, Sami</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-e9641b973338f23e4db53d710c451ae9949141247a53e84c69ff78df1a6112233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Algorithms</topic><topic>Analysis</topic><topic>Animals</topic><topic>Automation</topic><topic>Axons</topic><topic>Axons - physiology</topic><topic>Biology and Life Sciences</topic><topic>Biomedical engineering</topic><topic>Computer and Information Sciences</topic><topic>Deep Learning</topic><topic>Diameters</topic><topic>Electron microscopy</topic><topic>Embedding</topic><topic>Histomorphometry</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Laboratory animals</topic><topic>Learning programs</topic><topic>Machine learning</topic><topic>Male</topic><topic>Mechanization</topic><topic>Median nerve</topic><topic>Median Nerve - physiology</topic><topic>Medicine and Health Sciences</topic><topic>Methods</topic><topic>Micrography</topic><topic>Microscopy</topic><topic>Myelin</topic><topic>Myelin Sheath - physiology</topic><topic>Nerve Regeneration - physiology</topic><topic>Nervous system</topic><topic>Osmium</topic><topic>Paraffin</topic><topic>Paraffins</topic><topic>Peripheral nerves</topic><topic>Peripheral Nerves - physiology</topic><topic>Photomicrographs</topic><topic>Physical Sciences</topic><topic>Rats</topic><topic>Reconstructive surgery</topic><topic>Research and Analysis Methods</topic><topic>Robustness</topic><topic>Sample preparation</topic><topic>Thickness</topic><topic>Toluidine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, Alison L</creatorcontrib><creatorcontrib>Hricz, Nicholas</creatorcontrib><creatorcontrib>Malapati, Harsha</creatorcontrib><creatorcontrib>von Guionneau, Nicholas</creatorcontrib><creatorcontrib>Wong, Michael</creatorcontrib><creatorcontrib>Harris, Thomas</creatorcontrib><creatorcontrib>Boudreau, Mathieu</creatorcontrib><creatorcontrib>Cohen-Adad, Julien</creatorcontrib><creatorcontrib>Tuffaha, Sami</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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However, there has been little investigation on implementation of automated programs for widespread use. Ideally such a program should be able to perform AH across imaging modalities and nerve states. AxonDeepSeg (ADS) is an open source deep learning program that has previously been validated in electron microscopy. We evaluated the robustness of ADS for peripheral nerve axonal histomorphometry in light micrographs prepared using two different methods.
Axon histomorphometry using ADS and manual analysis (gold-standard) was performed on light micrographs of naïve or regenerating rat median nerve cross-sections prepared with either toluidine-resin or osmium-paraffin embedding protocols. The parameters of interest included axon count, axon diameter, myelin thickness, and g-ratio.
Manual and automatic ADS axon counts demonstrated good agreement in naïve nerves and moderate agreement on regenerating nerves. There were small but consistent differences in measured axon diameter, myelin thickness and g-ratio; however, absolute differences were small. Both methods appropriately identified differences between naïve and regenerating nerves. ADS was faster than manual axon analysis.
Without any algorithm retraining, ADS was able to appropriately identify critical differences between naïve and regenerating nerves and work with different sample preparation methods of peripheral nerve light micrographs. While there were differences between absolute values between manual and ADS, ADS performed consistently and required much less time. ADS is an accessible and robust tool for AH that can provide consistent analysis across protocols and nerve states.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>34234376</pmid><doi>10.1371/journal.pone.0248323</doi><tpages>e0248323</tpages><orcidid>https://orcid.org/0000-0003-3662-9532</orcidid><orcidid>https://orcid.org/0000-0002-9697-9799</orcidid><orcidid>https://orcid.org/0000-0003-4156-5748</orcidid><orcidid>https://orcid.org/0000-0003-0414-0556</orcidid><orcidid>https://orcid.org/0000-0002-9819-221X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Analysis Animals Automation Axons Axons - physiology Biology and Life Sciences Biomedical engineering Computer and Information Sciences Deep Learning Diameters Electron microscopy Embedding Histomorphometry Image Processing, Computer-Assisted - methods Laboratory animals Learning programs Machine learning Male Mechanization Median nerve Median Nerve - physiology Medicine and Health Sciences Methods Micrography Microscopy Myelin Myelin Sheath - physiology Nerve Regeneration - physiology Nervous system Osmium Paraffin Paraffins Peripheral nerves Peripheral Nerves - physiology Photomicrographs Physical Sciences Rats Reconstructive surgery Research and Analysis Methods Robustness Sample preparation Thickness Toluidine |
title | A simple and robust method for automating analysis of naïve and regenerating peripheral nerves |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T14%3A20%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20simple%20and%20robust%20method%20for%20automating%20analysis%20of%20na%C3%AFve%20and%20regenerating%20peripheral%20nerves&rft.jtitle=PloS%20one&rft.au=Wong,%20Alison%20L&rft.date=2021-07-07&rft.volume=16&rft.issue=7&rft.spage=e0248323&rft.pages=e0248323-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0248323&rft_dat=%3Cgale_plos_%3EA667732886%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2549192034&rft_id=info:pmid/34234376&rft_galeid=A667732886&rft_doaj_id=oai_doaj_org_article_1ee9b4bd1e4a4c92b5b7b3c9e2a7f800&rfr_iscdi=true |