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Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis
INTRODUCTION: Behavioral symptoms are commonly reported by patients with primary biliary cholangitis (PBC). In other patient populations, symptoms are commonly associated with hippocampal volume reduction linked to neuroinflammation (inferred from regional iron deposition), as demonstrated by magnet...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033882/ https://www.ncbi.nlm.nih.gov/pubmed/29977030 http://dx.doi.org/10.1038/s41424-018-0038-z |
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author | Mosher, Victoria A. L. Swain, Mark G. Pang, Jack X. Q. Kaplan, Gilaad G. Sharkey, Keith A. MacQueen, Glenda M. Goodyear, Bradley G. |
author_facet | Mosher, Victoria A. L. Swain, Mark G. Pang, Jack X. Q. Kaplan, Gilaad G. Sharkey, Keith A. MacQueen, Glenda M. Goodyear, Bradley G. |
author_sort | Mosher, Victoria A. L. |
collection | PubMed |
description | INTRODUCTION: Behavioral symptoms are commonly reported by patients with primary biliary cholangitis (PBC). In other patient populations, symptoms are commonly associated with hippocampal volume reduction linked to neuroinflammation (inferred from regional iron deposition), as demonstrated by magnetic resonance imaging (MRI). We hypothesized that PBC patients would exhibit reduced volume and increased iron deposition of the hippocampus. METHODS: Seventeen female non-cirrhotic PBC patients and 17 age/gender-matched controls underwent 3-Tesla T(1)-weighted MRI and quantitative susceptibility mapping (QSM; an indicator of iron deposition). The hippocampus and its subfields were segmented from T(1) images using Freesurfer, and susceptibility of the whole hippocampus was calculated from QSM images. Volume and susceptibility were compared between groups, and associations with PBC-40 score and disease indicators (years since diagnosis, Fibroscan value, alkaline phosphatase level, clinical response to ursodeoxycholic acid (UDCA)) were investigated. RESULTS: PBC patients exhibited significantly reduced hippocampal volume (p = 0.023) and increased susceptibility (p = 0.048). Subfield volumes were reduced for the subiculum, molecular layer, granule cell layer of the dentate gyrus and CA4 (p < 0.05). Fibroscan value was significantly correlated with PBC-40 (Spearman’s rho = 0.499; p = 0.041) and disease duration (Spearman’s rho = 0.568; p = 0.017). DISCUSSION: Our findings suggest hippocampal changes occur early in the disease course of PBC, similar in magnitude to those observed in major depressive disorder and neurodegenerative diseases. TRANSLATIONAL IMPACT: Clinical management of PBC could include early interventional strategies that promote hippocampal neurogenesis that may beneficially impact behavioral symptoms and improve quality of life. |
format | Online Article Text |
id | pubmed-6033882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-60338822018-07-06 Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis Mosher, Victoria A. L. Swain, Mark G. Pang, Jack X. Q. Kaplan, Gilaad G. Sharkey, Keith A. MacQueen, Glenda M. Goodyear, Bradley G. Clin Transl Gastroenterol Article INTRODUCTION: Behavioral symptoms are commonly reported by patients with primary biliary cholangitis (PBC). In other patient populations, symptoms are commonly associated with hippocampal volume reduction linked to neuroinflammation (inferred from regional iron deposition), as demonstrated by magnetic resonance imaging (MRI). We hypothesized that PBC patients would exhibit reduced volume and increased iron deposition of the hippocampus. METHODS: Seventeen female non-cirrhotic PBC patients and 17 age/gender-matched controls underwent 3-Tesla T(1)-weighted MRI and quantitative susceptibility mapping (QSM; an indicator of iron deposition). The hippocampus and its subfields were segmented from T(1) images using Freesurfer, and susceptibility of the whole hippocampus was calculated from QSM images. Volume and susceptibility were compared between groups, and associations with PBC-40 score and disease indicators (years since diagnosis, Fibroscan value, alkaline phosphatase level, clinical response to ursodeoxycholic acid (UDCA)) were investigated. RESULTS: PBC patients exhibited significantly reduced hippocampal volume (p = 0.023) and increased susceptibility (p = 0.048). Subfield volumes were reduced for the subiculum, molecular layer, granule cell layer of the dentate gyrus and CA4 (p < 0.05). Fibroscan value was significantly correlated with PBC-40 (Spearman’s rho = 0.499; p = 0.041) and disease duration (Spearman’s rho = 0.568; p = 0.017). DISCUSSION: Our findings suggest hippocampal changes occur early in the disease course of PBC, similar in magnitude to those observed in major depressive disorder and neurodegenerative diseases. TRANSLATIONAL IMPACT: Clinical management of PBC could include early interventional strategies that promote hippocampal neurogenesis that may beneficially impact behavioral symptoms and improve quality of life. Nature Publishing Group US 2018-07-06 /pmc/articles/PMC6033882/ /pubmed/29977030 http://dx.doi.org/10.1038/s41424-018-0038-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mosher, Victoria A. L. Swain, Mark G. Pang, Jack X. Q. Kaplan, Gilaad G. Sharkey, Keith A. MacQueen, Glenda M. Goodyear, Bradley G. Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
title | Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
title_full | Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
title_fullStr | Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
title_full_unstemmed | Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
title_short | Magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
title_sort | magnetic resonance imaging evidence of hippocampal structural changes in patients with primary biliary cholangitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033882/ https://www.ncbi.nlm.nih.gov/pubmed/29977030 http://dx.doi.org/10.1038/s41424-018-0038-z |
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