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Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies
OBJECTIVES: Diffusion‐weighted imaging (DWI) can reflect histopathologic changes in muscle disorders. The present study sought to elucidate possible associations between histopathology derived from muscle biopsies and DWI in myositis and other myopathies. METHODS: Nineteen patients (10 women, 52.6%)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667360/ https://www.ncbi.nlm.nih.gov/pubmed/32860496 http://dx.doi.org/10.1002/brb3.1809 |
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author | Meyer, Hans‐Jonas Schneider, Ilka Emmer, Alexander Kornhuber, Malte Surov, Alexey |
author_facet | Meyer, Hans‐Jonas Schneider, Ilka Emmer, Alexander Kornhuber, Malte Surov, Alexey |
author_sort | Meyer, Hans‐Jonas |
collection | PubMed |
description | OBJECTIVES: Diffusion‐weighted imaging (DWI) can reflect histopathologic changes in muscle disorders. The present study sought to elucidate possible associations between histopathology derived from muscle biopsies and DWI in myositis and other myopathies. METHODS: Nineteen patients (10 women, 52.6%) with a mean age 51.43 ± 19 years were included in this retrospective study. Apparent diffusion coefficients (ADC) were evaluated with a histogram approach of the biopsied muscle. The histopathology analysis included the scoring systems proposed by Tateyama et al., Fanin et al., Allenbach et al. and immunhistochemical stainings for MHC, CD68, CD8, and CD4. RESULTS: There was a tendency that skewness was lowered with increasing Tateyama score, but it did not reach statistical significance (p = .14). No statistical differences for the other scores were identified. There was a tendency that kurtosis was higher in MHC negative stained patient compared to positive patients, but statistically significance was not reached (p = .07). ADC histogram parameters did not correlate with CD68 and CD8 positive stained cells. There was a trend for skewness to correlate with the amount of CD4‐positive cells (r = .57, p = .07). CONCLUSION: The present study could not identify statistical significant associations between DWI and histopathology in muscle diseases based upon a small patient sample. Presumably, the investigated histopathology scores are more specific for certain disease aspects, whereas ADC values reflect the whole cellularity of the investigated muscle, which might cause the negative results. |
format | Online Article Text |
id | pubmed-7667360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76673602020-11-20 Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies Meyer, Hans‐Jonas Schneider, Ilka Emmer, Alexander Kornhuber, Malte Surov, Alexey Brain Behav Original Research OBJECTIVES: Diffusion‐weighted imaging (DWI) can reflect histopathologic changes in muscle disorders. The present study sought to elucidate possible associations between histopathology derived from muscle biopsies and DWI in myositis and other myopathies. METHODS: Nineteen patients (10 women, 52.6%) with a mean age 51.43 ± 19 years were included in this retrospective study. Apparent diffusion coefficients (ADC) were evaluated with a histogram approach of the biopsied muscle. The histopathology analysis included the scoring systems proposed by Tateyama et al., Fanin et al., Allenbach et al. and immunhistochemical stainings for MHC, CD68, CD8, and CD4. RESULTS: There was a tendency that skewness was lowered with increasing Tateyama score, but it did not reach statistical significance (p = .14). No statistical differences for the other scores were identified. There was a tendency that kurtosis was higher in MHC negative stained patient compared to positive patients, but statistically significance was not reached (p = .07). ADC histogram parameters did not correlate with CD68 and CD8 positive stained cells. There was a trend for skewness to correlate with the amount of CD4‐positive cells (r = .57, p = .07). CONCLUSION: The present study could not identify statistical significant associations between DWI and histopathology in muscle diseases based upon a small patient sample. Presumably, the investigated histopathology scores are more specific for certain disease aspects, whereas ADC values reflect the whole cellularity of the investigated muscle, which might cause the negative results. John Wiley and Sons Inc. 2020-08-29 /pmc/articles/PMC7667360/ /pubmed/32860496 http://dx.doi.org/10.1002/brb3.1809 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Meyer, Hans‐Jonas Schneider, Ilka Emmer, Alexander Kornhuber, Malte Surov, Alexey Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
title | Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
title_full | Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
title_fullStr | Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
title_full_unstemmed | Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
title_short | Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
title_sort | associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667360/ https://www.ncbi.nlm.nih.gov/pubmed/32860496 http://dx.doi.org/10.1002/brb3.1809 |
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