Cargando…
A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers
BACKGROUND: Multispectral microscopy and multiple staining can be used to identify cells with distinct immunohistochemical (IHC) characteristics. We present here a method called hypothesized interaction distribution (HID) analysis for characterizing the statistical distribution of pair-wise spatial...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678742/ https://www.ncbi.nlm.nih.gov/pubmed/23766940 http://dx.doi.org/10.4103/2153-3539.109856 |
_version_ | 1782272893291331584 |
---|---|
author | Rose, Chris J. Naidoo, Khimara Clay, Vanessa Linton, Kim Radford, John A. Byers, Richard J. |
author_facet | Rose, Chris J. Naidoo, Khimara Clay, Vanessa Linton, Kim Radford, John A. Byers, Richard J. |
author_sort | Rose, Chris J. |
collection | PubMed |
description | BACKGROUND: Multispectral microscopy and multiple staining can be used to identify cells with distinct immunohistochemical (IHC) characteristics. We present here a method called hypothesized interaction distribution (HID) analysis for characterizing the statistical distribution of pair-wise spatial relationships between cells with particular IHC characteristics and apply it to clinical data. MATERIALS AND METHODS: We retrospectively analyzed data from a study of 26 follicular lymphoma patients in which sections were stained for CD20 and YY1. HID analysis, using leave-one-out validation, was used to assign patients to one of two groups. We tested the null hypothesis of no difference in Kaplan–Meier survival curves between the groups. RESULTS: Shannon entropy of HIDs assigned patients to groups that had significantly different survival curves (median survival was 7.70 versus 110 months, P = 0.00750). Hypothesized interactions between pairs of cells positive for both CD20 and YY1 were associated with poor survival. CONCLUSIONS: HID analysis provides quantitative inferences about possible interactions between spatially proximal cells with particular IHC characteristics. In follicular lymphoma, HID analysis was able to distinguish between patients with poor versus good survival, and it may have diagnostic and prognostic utility in this and other diseases. |
format | Online Article Text |
id | pubmed-3678742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36787422013-06-13 A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers Rose, Chris J. Naidoo, Khimara Clay, Vanessa Linton, Kim Radford, John A. Byers, Richard J. J Pathol Inform Symposium - Original Research BACKGROUND: Multispectral microscopy and multiple staining can be used to identify cells with distinct immunohistochemical (IHC) characteristics. We present here a method called hypothesized interaction distribution (HID) analysis for characterizing the statistical distribution of pair-wise spatial relationships between cells with particular IHC characteristics and apply it to clinical data. MATERIALS AND METHODS: We retrospectively analyzed data from a study of 26 follicular lymphoma patients in which sections were stained for CD20 and YY1. HID analysis, using leave-one-out validation, was used to assign patients to one of two groups. We tested the null hypothesis of no difference in Kaplan–Meier survival curves between the groups. RESULTS: Shannon entropy of HIDs assigned patients to groups that had significantly different survival curves (median survival was 7.70 versus 110 months, P = 0.00750). Hypothesized interactions between pairs of cells positive for both CD20 and YY1 were associated with poor survival. CONCLUSIONS: HID analysis provides quantitative inferences about possible interactions between spatially proximal cells with particular IHC characteristics. In follicular lymphoma, HID analysis was able to distinguish between patients with poor versus good survival, and it may have diagnostic and prognostic utility in this and other diseases. Medknow Publications & Media Pvt Ltd 2013-03-30 /pmc/articles/PMC3678742/ /pubmed/23766940 http://dx.doi.org/10.4103/2153-3539.109856 Text en Copyright: © 2013 Rose CJ. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Symposium - Original Research Rose, Chris J. Naidoo, Khimara Clay, Vanessa Linton, Kim Radford, John A. Byers, Richard J. A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
title | A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
title_full | A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
title_fullStr | A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
title_full_unstemmed | A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
title_short | A statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
title_sort | statistical framework for analyzing hypothesized interactions between cells imaged using multispectral microscopy and multiple immunohistochemical markers |
topic | Symposium - Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678742/ https://www.ncbi.nlm.nih.gov/pubmed/23766940 http://dx.doi.org/10.4103/2153-3539.109856 |
work_keys_str_mv | AT rosechrisj astatisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT naidookhimara astatisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT clayvanessa astatisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT lintonkim astatisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT radfordjohna astatisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT byersrichardj astatisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT rosechrisj statisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT naidookhimara statisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT clayvanessa statisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT lintonkim statisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT radfordjohna statisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers AT byersrichardj statisticalframeworkforanalyzinghypothesizedinteractionsbetweencellsimagedusingmultispectralmicroscopyandmultipleimmunohistochemicalmarkers |