Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele.
Neural tube defects are a common congenital anomaly involving incomplete closure of the spinal cord. Myelomeningocele (MMC) is a severe form in which there is complete exposure of neural tissue with a lack of skin, soft tissue, or bony covering to protect the spinal cord. The all-trans retinoic acid...
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2021
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oai:doaj.org-article:9e25c29e5daa41eb862d55f65b30fd532021-12-02T20:15:43ZDiffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele.1932-620310.1371/journal.pone.0253583https://doaj.org/article/9e25c29e5daa41eb862d55f65b30fd532021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0253583https://doaj.org/toc/1932-6203Neural tube defects are a common congenital anomaly involving incomplete closure of the spinal cord. Myelomeningocele (MMC) is a severe form in which there is complete exposure of neural tissue with a lack of skin, soft tissue, or bony covering to protect the spinal cord. The all-trans retinoic acid (ATRA) induced rat model of (MMC) is a reproducible, cost-effective means of studying this disease; however, there are limited modalities to objectively quantify disease severity, or potential benefits from experimental therapies. We sought to determine the feasibility of detecting differences between MMC and wild type (WT) rat fetuses using diffusion magnetic resonance imaging techniques (MRI). Rat dams were gavage-fed ATRA to produce MMC defects in fetuses, which were surgically delivered prior to term. Average diffusion coefficient (ADC) and fractional anisotropy (FA) maps were obtained for each fetus. Brain volumes and two anatomically defined brain length measurements (D1 and D2) were significantly decreased in MMC compared to WT. Mean ADC signal was significantly increased in MMC compared to WT, but no difference was found for FA signal. In summary, ADC and brain measurements were significantly different between WT and MMC rat fetuses. ADC could be a useful complementary imaging biomarker to current histopathologic analysis of MMC models, and potentially expedite therapeutic research for this disease.Nathan MaasselJames FarrellyDaniel ComanMollie Freedman-WeissSamantha AhleSarah UllrichNicholas YungFahmeed HyderDavid StitelmanPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 6, p e0253583 (2021) |
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Medicine R Science Q Nathan Maassel James Farrelly Daniel Coman Mollie Freedman-Weiss Samantha Ahle Sarah Ullrich Nicholas Yung Fahmeed Hyder David Stitelman Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
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Neural tube defects are a common congenital anomaly involving incomplete closure of the spinal cord. Myelomeningocele (MMC) is a severe form in which there is complete exposure of neural tissue with a lack of skin, soft tissue, or bony covering to protect the spinal cord. The all-trans retinoic acid (ATRA) induced rat model of (MMC) is a reproducible, cost-effective means of studying this disease; however, there are limited modalities to objectively quantify disease severity, or potential benefits from experimental therapies. We sought to determine the feasibility of detecting differences between MMC and wild type (WT) rat fetuses using diffusion magnetic resonance imaging techniques (MRI). Rat dams were gavage-fed ATRA to produce MMC defects in fetuses, which were surgically delivered prior to term. Average diffusion coefficient (ADC) and fractional anisotropy (FA) maps were obtained for each fetus. Brain volumes and two anatomically defined brain length measurements (D1 and D2) were significantly decreased in MMC compared to WT. Mean ADC signal was significantly increased in MMC compared to WT, but no difference was found for FA signal. In summary, ADC and brain measurements were significantly different between WT and MMC rat fetuses. ADC could be a useful complementary imaging biomarker to current histopathologic analysis of MMC models, and potentially expedite therapeutic research for this disease. |
format |
article |
author |
Nathan Maassel James Farrelly Daniel Coman Mollie Freedman-Weiss Samantha Ahle Sarah Ullrich Nicholas Yung Fahmeed Hyder David Stitelman |
author_facet |
Nathan Maassel James Farrelly Daniel Coman Mollie Freedman-Weiss Samantha Ahle Sarah Ullrich Nicholas Yung Fahmeed Hyder David Stitelman |
author_sort |
Nathan Maassel |
title |
Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
title_short |
Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
title_full |
Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
title_fullStr |
Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
title_full_unstemmed |
Diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
title_sort |
diffusion weighted imaging as a biomarker of retinoic acid induced myelomeningocele. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2021 |
url |
https://doaj.org/article/9e25c29e5daa41eb862d55f65b30fd53 |
work_keys_str_mv |
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1718374543176761344 |