Cargando…
Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model
BACKGROUND: Chronic airway fibrosis (CAF) is the most prevalent complication in human lung transplant recipients. The aim of the study is to evaluate magnetisation transfer (MT) as a biomarker of developing CAF of lung transplants in a mouse model. METHODS: Lung transplantation was performed in 48 m...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909363/ https://www.ncbi.nlm.nih.gov/pubmed/29708209 http://dx.doi.org/10.1186/s41747-017-0032-3 |
_version_ | 1783315888471015424 |
---|---|
author | Kenkel, David Yamada, Yoshito Weiger, Markus Wurnig, Moritz C. Jungraithmayr, Wolfgang Boss, Andreas |
author_facet | Kenkel, David Yamada, Yoshito Weiger, Markus Wurnig, Moritz C. Jungraithmayr, Wolfgang Boss, Andreas |
author_sort | Kenkel, David |
collection | PubMed |
description | BACKGROUND: Chronic airway fibrosis (CAF) is the most prevalent complication in human lung transplant recipients. The aim of the study is to evaluate magnetisation transfer (MT) as a biomarker of developing CAF of lung transplants in a mouse model. METHODS: Lung transplantation was performed in 48 mice, applying major or minor histocompatibility mismatches between strains for the induction of CAF. MT measurements were performed in vivo with systematic variation of off-resonance frequencies and flip angle of the MT prepulse. MT ratios (MTRs) were compared for lungs showing CAF and without CAF. RESULTS: Seven out of 24 animals (29%) showed a pattern of CAF at histology. All mice developing CAF also showed signs of acute rejection, whereas none of the lungs showed signs of other post-transplant complications. After lung transplantation, pulmonary infiltration was a frequent finding (14 out of 24) exhibiting a higher MTR (24.8% ± 4.5%) compared to well-ventilated lungs (12.3% ± 6.9%, p = 0.001) at 8000 Hz off-resonance frequency, 3000° flip angle. In infiltrated lung tissue exhibiting CAF, lower MTR values (21.8% ± 5.7%) were found compared to infiltrated lungs showing signs of acute rejection alone (26.5% ± 2.9%, p = 0.028), at 8000 Hz, 3000° flip angle. The highest MTR values were observed at 3000° flip angle, using a 1000 Hz off-resonance frequency. CONCLUSION: MTR might serve as a tool for the detection of CAF in infiltrated lung tissue. |
format | Online Article Text |
id | pubmed-5909363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-59093632018-04-24 Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model Kenkel, David Yamada, Yoshito Weiger, Markus Wurnig, Moritz C. Jungraithmayr, Wolfgang Boss, Andreas Eur Radiol Exp Original Article BACKGROUND: Chronic airway fibrosis (CAF) is the most prevalent complication in human lung transplant recipients. The aim of the study is to evaluate magnetisation transfer (MT) as a biomarker of developing CAF of lung transplants in a mouse model. METHODS: Lung transplantation was performed in 48 mice, applying major or minor histocompatibility mismatches between strains for the induction of CAF. MT measurements were performed in vivo with systematic variation of off-resonance frequencies and flip angle of the MT prepulse. MT ratios (MTRs) were compared for lungs showing CAF and without CAF. RESULTS: Seven out of 24 animals (29%) showed a pattern of CAF at histology. All mice developing CAF also showed signs of acute rejection, whereas none of the lungs showed signs of other post-transplant complications. After lung transplantation, pulmonary infiltration was a frequent finding (14 out of 24) exhibiting a higher MTR (24.8% ± 4.5%) compared to well-ventilated lungs (12.3% ± 6.9%, p = 0.001) at 8000 Hz off-resonance frequency, 3000° flip angle. In infiltrated lung tissue exhibiting CAF, lower MTR values (21.8% ± 5.7%) were found compared to infiltrated lungs showing signs of acute rejection alone (26.5% ± 2.9%, p = 0.028), at 8000 Hz, 3000° flip angle. The highest MTR values were observed at 3000° flip angle, using a 1000 Hz off-resonance frequency. CONCLUSION: MTR might serve as a tool for the detection of CAF in infiltrated lung tissue. Springer International Publishing 2018-02-12 /pmc/articles/PMC5909363/ /pubmed/29708209 http://dx.doi.org/10.1186/s41747-017-0032-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Kenkel, David Yamada, Yoshito Weiger, Markus Wurnig, Moritz C. Jungraithmayr, Wolfgang Boss, Andreas Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
title | Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
title_full | Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
title_fullStr | Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
title_full_unstemmed | Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
title_short | Magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
title_sort | magnetisation transfer as a biomarker for chronic airway fibrosis in a mouse lung transplantation model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909363/ https://www.ncbi.nlm.nih.gov/pubmed/29708209 http://dx.doi.org/10.1186/s41747-017-0032-3 |
work_keys_str_mv | AT kenkeldavid magnetisationtransferasabiomarkerforchronicairwayfibrosisinamouselungtransplantationmodel AT yamadayoshito magnetisationtransferasabiomarkerforchronicairwayfibrosisinamouselungtransplantationmodel AT weigermarkus magnetisationtransferasabiomarkerforchronicairwayfibrosisinamouselungtransplantationmodel AT wurnigmoritzc magnetisationtransferasabiomarkerforchronicairwayfibrosisinamouselungtransplantationmodel AT jungraithmayrwolfgang magnetisationtransferasabiomarkerforchronicairwayfibrosisinamouselungtransplantationmodel AT bossandreas magnetisationtransferasabiomarkerforchronicairwayfibrosisinamouselungtransplantationmodel |