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Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease

BACKGROUND: End-stage renal disease (ESRD) patients have functional and structural brain abnormalities. The cerebellum also showed varying degrees of damage. However, no studies on cerebellar-cerebral functional connectivity (FC) have been conducted in ESRD patients. This study aimed to investigate...

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Autores principales: Fang, Jie, Miao, Yingying, Zou, Fan, Liu, Yarui, Zuo, Jiangle, Qi, Xiangming, Wang, Haibao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392254/
https://www.ncbi.nlm.nih.gov/pubmed/37488933
http://dx.doi.org/10.1080/0886022X.2023.2238829
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author Fang, Jie
Miao, Yingying
Zou, Fan
Liu, Yarui
Zuo, Jiangle
Qi, Xiangming
Wang, Haibao
author_facet Fang, Jie
Miao, Yingying
Zou, Fan
Liu, Yarui
Zuo, Jiangle
Qi, Xiangming
Wang, Haibao
author_sort Fang, Jie
collection PubMed
description BACKGROUND: End-stage renal disease (ESRD) patients have functional and structural brain abnormalities. The cerebellum also showed varying degrees of damage. However, no studies on cerebellar-cerebral functional connectivity (FC) have been conducted in ESRD patients. This study aimed to investigate the changes in cerebellar-cerebral FC in ESRD patients and its relationship with neuropsychological and clinical indexes. METHODS: Resting-state functional magnetic resonance imaging and neuropsychological assessment were performed on 37 ESRD patients and 35 control subjects. Seed-based FC analysis was performed to investigate inter-group differences in cerebellar-cerebral FC. In addition, the relations of altered FC with the neuropsychological function and clinical indicators were analyzed in ERSD patients. RESULTS: ESRD patients exhibited alterations in cerebellar-cerebral FC involving the executive control network, default mode network, and affective-limbic network compared to control subjects (False discovery rate-corrected, p < 0.05). The altered cerebellar-cerebral FC was associated with the Montreal Cognitive Assessment Scale score (p < 0.05), and correlated with serum creatinine and uric acid levels within the ESRD group (p < 0.05). CONCLUSIONS: The study indicates that cerebellar-cerebral FC is involved in the neural substrates of cognitive impairment in ESRD patients. The findings may provide clinically relevant new neuroimaging biomarkers for the neuropathological mechanisms underlying cognitive impairment of ESRD.
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spelling pubmed-103922542023-08-02 Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease Fang, Jie Miao, Yingying Zou, Fan Liu, Yarui Zuo, Jiangle Qi, Xiangming Wang, Haibao Ren Fail Research Article BACKGROUND: End-stage renal disease (ESRD) patients have functional and structural brain abnormalities. The cerebellum also showed varying degrees of damage. However, no studies on cerebellar-cerebral functional connectivity (FC) have been conducted in ESRD patients. This study aimed to investigate the changes in cerebellar-cerebral FC in ESRD patients and its relationship with neuropsychological and clinical indexes. METHODS: Resting-state functional magnetic resonance imaging and neuropsychological assessment were performed on 37 ESRD patients and 35 control subjects. Seed-based FC analysis was performed to investigate inter-group differences in cerebellar-cerebral FC. In addition, the relations of altered FC with the neuropsychological function and clinical indicators were analyzed in ERSD patients. RESULTS: ESRD patients exhibited alterations in cerebellar-cerebral FC involving the executive control network, default mode network, and affective-limbic network compared to control subjects (False discovery rate-corrected, p < 0.05). The altered cerebellar-cerebral FC was associated with the Montreal Cognitive Assessment Scale score (p < 0.05), and correlated with serum creatinine and uric acid levels within the ESRD group (p < 0.05). CONCLUSIONS: The study indicates that cerebellar-cerebral FC is involved in the neural substrates of cognitive impairment in ESRD patients. The findings may provide clinically relevant new neuroimaging biomarkers for the neuropathological mechanisms underlying cognitive impairment of ESRD. Taylor & Francis 2023-07-24 /pmc/articles/PMC10392254/ /pubmed/37488933 http://dx.doi.org/10.1080/0886022X.2023.2238829 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Article
Fang, Jie
Miao, Yingying
Zou, Fan
Liu, Yarui
Zuo, Jiangle
Qi, Xiangming
Wang, Haibao
Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
title Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
title_full Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
title_fullStr Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
title_full_unstemmed Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
title_short Altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
title_sort altered resting-state cerebellar-cerebral functional connectivity in patients with end-stage renal disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392254/
https://www.ncbi.nlm.nih.gov/pubmed/37488933
http://dx.doi.org/10.1080/0886022X.2023.2238829
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