Atlas-based liver segmentation for nonhuman primate research.


Journal

International journal of computer assisted radiology and surgery
ISSN: 1861-6429
Titre abrégé: Int J Comput Assist Radiol Surg
Pays: Germany
ID NLM: 101499225

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 27 02 2020
accepted: 30 06 2020
pubmed: 11 7 2020
medline: 23 2 2021
entrez: 11 7 2020
Statut: ppublish

Résumé

Certain viral infectious diseases cause systemic damage and the liver is an important organ affected directly by the virus and/or the hosts' response to the virus. Medical imaging indicates that the liver damage is heterogenous, and therefore, quantification of these changes requires analysis of the entire organ. Delineating the liver in preclinical imaging studies is a time-consuming and difficult task that would benefit from automated liver segmentation. A nonhuman primate atlas-based liver segmentation method was developed to support quantitative image analysis of preclinical research. A set of 82 computed tomography (CT) scans of nonhuman primates with associated manual contours delineating the liver was generated from normal and abnormal livers. The proposed technique uses rigid and deformable registrations, a majority vote algorithm, and image post-processing operations to automate the liver segmentation process. This technique was evaluated using Dice similarity, Hausdorff distance measures, and Bland-Altman plots. Automated segmentation results compare favorably with manual contouring, achieving a median Dice score of 0.91. Limits of agreement from Bland-Altman plots indicate that liver changes of 3 Hounsfield units (CT) and 0.4 SUVmean (positron emission tomography) are detectable using our automated method of segmentation, which are substantially less than changes observed in the host response to these viral infectious diseases. The proposed atlas-based liver segmentation technique is generalizable to various sizes and species of nonhuman primates and facilitates preclinical infectious disease research studies. While the image analysis software used is commercially available and facilities with funding can access the software to perform similar nonhuman primate liver quantitative analyses, the approach can be implemented in open-source frameworks as there is nothing proprietary about these methods.

Identifiants

pubmed: 32648161
doi: 10.1007/s11548-020-02225-9
pii: 10.1007/s11548-020-02225-9
pmc: PMC7502527
mid: NIHMS1611687
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1631-1638

Subventions

Organisme : CCR NIH HHS
ID : HHSN261200800001C
Pays : United States
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272200700016I
Pays : United States

Références

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pubmed: 27043611
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pubmed: 28096782
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pubmed: 30194472

Auteurs

Jeffrey Solomon (J)

Clinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research Sponsored by the National Cancer Institute, Frederick, MD, USA. jeffrey.solomon@nih.gov.
Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA. jeffrey.solomon@nih.gov.

Nina Aiosa (N)

Center for Infectious Disease Imaging, Clinical Center, Radiology and Imaging Sciences, National Institutes of Health, Bethesda, MD, USA.

Dara Bradley (D)

Center for Infectious Disease Imaging, Clinical Center, Radiology and Imaging Sciences, National Institutes of Health, Bethesda, MD, USA.

Marcelo A Castro (MA)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Syed Reza (S)

Center for Infectious Disease Imaging, Clinical Center, Radiology and Imaging Sciences, National Institutes of Health, Bethesda, MD, USA.

Christopher Bartos (C)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Philip Sayre (P)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Ji Hyun Lee (JH)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Jennifer Sword (J)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Michael R Holbrook (MR)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Richard S Bennett (RS)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Dima A Hammoud (DA)

Center for Infectious Disease Imaging, Clinical Center, Radiology and Imaging Sciences, National Institutes of Health, Bethesda, MD, USA.

Reed F Johnson (RF)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

Irwin Feuerstein (I)

Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD, USA.

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Classifications MeSH