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Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates
BACKGROUND: Preliminary studies have shown that diffusion tensor imaging (DTI) is helpful in evaluating liver disorders. However, there is no published literature on the use of DTI in the diagnosis of biliary atresia (BA). This study aimed to investigate the diagnostic value of the liver average app...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167545/ https://www.ncbi.nlm.nih.gov/pubmed/27992499 http://dx.doi.org/10.1371/journal.pone.0168477 |
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author | Liu, Bo Cai, Jinhua Zhu, Jin Zheng, Helin Zhang, Yun Wang, Longlun |
author_facet | Liu, Bo Cai, Jinhua Zhu, Jin Zheng, Helin Zhang, Yun Wang, Longlun |
author_sort | Liu, Bo |
collection | PubMed |
description | BACKGROUND: Preliminary studies have shown that diffusion tensor imaging (DTI) is helpful in evaluating liver disorders. However, there is no published literature on the use of DTI in the diagnosis of biliary atresia (BA). This study aimed to investigate the diagnostic value of the liver average apparent diffusion coefficient (ADC) and fractional anisotropy (FA) measured using DTI for BA in neonates and infants. METHODS: Fifty-nine patients with infant jaundice were included in this study. DTI was performed with b factors of 0 and 1000 s/mm(2). Liver fibrosis in the BA group was determined and graded (F0, F1, F2, F3, F4) based on the pathological findings. Statistical analyses were performed to determine the diagnostic accuracy of DTI for BA. RESULTS: The ADC value was significantly lower in the BA group [(1.262±0.127)×10(−3) mm(2)/s] than in the non-BA group [(1.430±0.149)×10(−3) mm(2)/s, (P<0.001)]. The area under the receiver operating characteristic curve was 0.805±0.058 (P<0.001) for ADC. With a cut-off value of 1.317×10(−3) mm(2)/s, ADC achieved a sensitivity of 75% and a specificity of 81.5% for the differential diagnosis of BA and non-BA. In the BA group, the ADC value was significantly correlated with fibrotic stage. Further analysis showed that the ADC value of stage F0 was significantly higher than that of stages F1, F2, F3 and F4, whereas there were no significant differences among stages F1, F2, F3 and F4. CONCLUSION: Hepatic ADC measured with DTI can be used as an adjunct to other noninvasive imaging methods in the differential diagnosis of BA and non-BA. ADC was helpful in detecting liver fibrosis but not in differentiating the fibrotic grades. |
format | Online Article Text |
id | pubmed-5167545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51675452017-01-04 Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates Liu, Bo Cai, Jinhua Zhu, Jin Zheng, Helin Zhang, Yun Wang, Longlun PLoS One Research Article BACKGROUND: Preliminary studies have shown that diffusion tensor imaging (DTI) is helpful in evaluating liver disorders. However, there is no published literature on the use of DTI in the diagnosis of biliary atresia (BA). This study aimed to investigate the diagnostic value of the liver average apparent diffusion coefficient (ADC) and fractional anisotropy (FA) measured using DTI for BA in neonates and infants. METHODS: Fifty-nine patients with infant jaundice were included in this study. DTI was performed with b factors of 0 and 1000 s/mm(2). Liver fibrosis in the BA group was determined and graded (F0, F1, F2, F3, F4) based on the pathological findings. Statistical analyses were performed to determine the diagnostic accuracy of DTI for BA. RESULTS: The ADC value was significantly lower in the BA group [(1.262±0.127)×10(−3) mm(2)/s] than in the non-BA group [(1.430±0.149)×10(−3) mm(2)/s, (P<0.001)]. The area under the receiver operating characteristic curve was 0.805±0.058 (P<0.001) for ADC. With a cut-off value of 1.317×10(−3) mm(2)/s, ADC achieved a sensitivity of 75% and a specificity of 81.5% for the differential diagnosis of BA and non-BA. In the BA group, the ADC value was significantly correlated with fibrotic stage. Further analysis showed that the ADC value of stage F0 was significantly higher than that of stages F1, F2, F3 and F4, whereas there were no significant differences among stages F1, F2, F3 and F4. CONCLUSION: Hepatic ADC measured with DTI can be used as an adjunct to other noninvasive imaging methods in the differential diagnosis of BA and non-BA. ADC was helpful in detecting liver fibrosis but not in differentiating the fibrotic grades. Public Library of Science 2016-12-19 /pmc/articles/PMC5167545/ /pubmed/27992499 http://dx.doi.org/10.1371/journal.pone.0168477 Text en © 2016 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Liu, Bo Cai, Jinhua Zhu, Jin Zheng, Helin Zhang, Yun Wang, Longlun Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates |
title | Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates |
title_full | Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates |
title_fullStr | Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates |
title_full_unstemmed | Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates |
title_short | Diffusion Tensor Imaging for Evaluating Biliary Atresia in Infants and Neonates |
title_sort | diffusion tensor imaging for evaluating biliary atresia in infants and neonates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167545/ https://www.ncbi.nlm.nih.gov/pubmed/27992499 http://dx.doi.org/10.1371/journal.pone.0168477 |
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