Cargando…

Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter

OBJECTIVES: Fatigue, itch, depressed mood, and cognitive impairment significantly impact the quality of life of many patients with primary biliary cholangitis (PBC). Previous neuroimaging studies of non-hepatic diseases suggest that these symptoms are often associated with dysfunction of deep gray m...

Descripción completa

Detalles Bibliográficos
Autores principales: Mosher, Victoria A L, Swain, Mark G, Pang, Jack X Q, Kaplan, Gilaad G, Sharkey, Keith A, MacQueen, Glenda M, Goodyear, Bradley G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539342/
https://www.ncbi.nlm.nih.gov/pubmed/28749455
http://dx.doi.org/10.1038/ctg.2017.34
_version_ 1783254472723529728
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 OBJECTIVES: Fatigue, itch, depressed mood, and cognitive impairment significantly impact the quality of life of many patients with primary biliary cholangitis (PBC). Previous neuroimaging studies of non-hepatic diseases suggest that these symptoms are often associated with dysfunction of deep gray matter brain regions. We used resting-state functional magnetic resonance imaging (rsfMRI) to determine whether PBC patients exhibit altered functional connections of deep gray matter. METHODS: Twenty female non-cirrhotic PBC patients and 21 age/gender-matched controls underwent rsfMRI. Resting-state functional connectivity (rsFC) of deep gray matter brain structures (putamen, thalamus, amygdala, hippocampus) was compared between groups. Fatigue, itch, mood, cognitive performance, and clinical response to ursodeoxycholic acid (UDCA) were assessed, and their association with rsFC was determined. RESULTS: Relative to controls, PBC patients exhibited significantly increased rsFC between the putamen, thalamus, amygdala, and hippocampus, as well as with frontal and parietal regions. Reduced rsFC of the putamen and hippocampus with motor and sensory regions of the brain were also observed. Fatigue, itch, complete response to UDCA, and verbal working memory performance were also associated with altered rsFC of deep gray matter. These rsFC changes were independent of biochemical disease severity. CONCLUSIONS: PBC patients have objective evidence of altered rsFC of the brain’s deep gray matter that is in part linked to fatigue severity, itch, response to UDCA therapy, and cognitive performance. These results may guide future approaches to define how PBC leads to altered brain connectivity and provide insight into novel targets for treating PBC-associated brain dysfunction and behavioral symptoms.
format Online
Article
Text
id pubmed-5539342
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-55393422017-08-04 Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter 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 Original Contributions OBJECTIVES: Fatigue, itch, depressed mood, and cognitive impairment significantly impact the quality of life of many patients with primary biliary cholangitis (PBC). Previous neuroimaging studies of non-hepatic diseases suggest that these symptoms are often associated with dysfunction of deep gray matter brain regions. We used resting-state functional magnetic resonance imaging (rsfMRI) to determine whether PBC patients exhibit altered functional connections of deep gray matter. METHODS: Twenty female non-cirrhotic PBC patients and 21 age/gender-matched controls underwent rsfMRI. Resting-state functional connectivity (rsFC) of deep gray matter brain structures (putamen, thalamus, amygdala, hippocampus) was compared between groups. Fatigue, itch, mood, cognitive performance, and clinical response to ursodeoxycholic acid (UDCA) were assessed, and their association with rsFC was determined. RESULTS: Relative to controls, PBC patients exhibited significantly increased rsFC between the putamen, thalamus, amygdala, and hippocampus, as well as with frontal and parietal regions. Reduced rsFC of the putamen and hippocampus with motor and sensory regions of the brain were also observed. Fatigue, itch, complete response to UDCA, and verbal working memory performance were also associated with altered rsFC of deep gray matter. These rsFC changes were independent of biochemical disease severity. CONCLUSIONS: PBC patients have objective evidence of altered rsFC of the brain’s deep gray matter that is in part linked to fatigue severity, itch, response to UDCA therapy, and cognitive performance. These results may guide future approaches to define how PBC leads to altered brain connectivity and provide insight into novel targets for treating PBC-associated brain dysfunction and behavioral symptoms. Nature Publishing Group 2017-07 2017-07-27 /pmc/articles/PMC5539342/ /pubmed/28749455 http://dx.doi.org/10.1038/ctg.2017.34 Text en Copyright © 2017 The Author(s) Official journal of the American College of Gastroenterology http://creativecommons.org/licenses/by-nc-nd/4.0/ Clinical and Translational Gastroenterology is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Contributions
Mosher, Victoria A L
Swain, Mark G
Pang, Jack X Q
Kaplan, Gilaad G
Sharkey, Keith A
MacQueen, Glenda M
Goodyear, Bradley G
Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter
title Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter
title_full Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter
title_fullStr Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter
title_full_unstemmed Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter
title_short Primary Biliary Cholangitis Alters Functional Connections of the Brain’s Deep Gray Matter
title_sort primary biliary cholangitis alters functional connections of the brain’s deep gray matter
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539342/
https://www.ncbi.nlm.nih.gov/pubmed/28749455
http://dx.doi.org/10.1038/ctg.2017.34
work_keys_str_mv AT moshervictoriaal primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter
AT swainmarkg primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter
AT pangjackxq primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter
AT kaplangilaadg primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter
AT sharkeykeitha primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter
AT macqueenglendam primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter
AT goodyearbradleyg primarybiliarycholangitisaltersfunctionalconnectionsofthebrainsdeepgraymatter