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Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study

INTRODUCTION: Respective alterations in resting-state brain neural activity and cerebral blood flow (CBF) in type 2 diabetes mellitus (T2DM) have been reported. However, their coupling alteration in T2DM remains largely unknown. RESEARCH DESIGN AND METHODS: Twenty-seven patients with T2DM aged 40–67...

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Autores principales: Zhang, Yang, Zhang, Xiaolu, Ma, Guangyang, Qin, Wen, Yang, Jiayang, Lin, Jiahui, Zhang, Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816934/
https://www.ncbi.nlm.nih.gov/pubmed/33462074
http://dx.doi.org/10.1136/bmjdrc-2020-001433
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author Zhang, Yang
Zhang, Xiaolu
Ma, Guangyang
Qin, Wen
Yang, Jiayang
Lin, Jiahui
Zhang, Quan
author_facet Zhang, Yang
Zhang, Xiaolu
Ma, Guangyang
Qin, Wen
Yang, Jiayang
Lin, Jiahui
Zhang, Quan
author_sort Zhang, Yang
collection PubMed
description INTRODUCTION: Respective alterations in resting-state brain neural activity and cerebral blood flow (CBF) in type 2 diabetes mellitus (T2DM) have been reported. However, their coupling alteration in T2DM remains largely unknown. RESEARCH DESIGN AND METHODS: Twenty-seven patients with T2DM aged 40–67 years and 36 well-matched healthy controls (HCs) underwent resting-state functional MRI (rs-fMRI) and arterial spin labeling (ASL) scans at two time points with a 5-year interval. Regional homogeneity (ReHo) and CBF were calculated from rs-fMRI and ASL, respectively. The standardized ReHo:CBF ratio (mReHo:mCBF ratio), the spontaneous neuronal activity per unit CBF supply, was compared between the two time points. Relationships between the mReHo:mCBF ratio and memory performance were analyzed. RESULTS: Over 5 years, decreased mReHo:mCBF ratios in patients with T2DM were mainly distributed in four regions, among which the left insula exhibited more severely decreased mReHo:mCBF ratio in patients with T2DM than in HCs, while the left postcentral gyrus, the right Rolandic operculum, and the right precentral gyrus showed no significant intergroup difference. Correlations between the mReHo:mCBF ratio and memory performance were also found in patients with T2DM. CONCLUSIONS: This study suggests that T2DM may accelerate neurovascular coupling impairment in specific brain regions (the left insula), contributing to memory decline. This study implies that the mReHo:mCBF ratio is a potential imaging marker for detecting neurovascular changes.
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spelling pubmed-78169342021-01-28 Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study Zhang, Yang Zhang, Xiaolu Ma, Guangyang Qin, Wen Yang, Jiayang Lin, Jiahui Zhang, Quan BMJ Open Diabetes Res Care Pathophysiology/Complications INTRODUCTION: Respective alterations in resting-state brain neural activity and cerebral blood flow (CBF) in type 2 diabetes mellitus (T2DM) have been reported. However, their coupling alteration in T2DM remains largely unknown. RESEARCH DESIGN AND METHODS: Twenty-seven patients with T2DM aged 40–67 years and 36 well-matched healthy controls (HCs) underwent resting-state functional MRI (rs-fMRI) and arterial spin labeling (ASL) scans at two time points with a 5-year interval. Regional homogeneity (ReHo) and CBF were calculated from rs-fMRI and ASL, respectively. The standardized ReHo:CBF ratio (mReHo:mCBF ratio), the spontaneous neuronal activity per unit CBF supply, was compared between the two time points. Relationships between the mReHo:mCBF ratio and memory performance were analyzed. RESULTS: Over 5 years, decreased mReHo:mCBF ratios in patients with T2DM were mainly distributed in four regions, among which the left insula exhibited more severely decreased mReHo:mCBF ratio in patients with T2DM than in HCs, while the left postcentral gyrus, the right Rolandic operculum, and the right precentral gyrus showed no significant intergroup difference. Correlations between the mReHo:mCBF ratio and memory performance were also found in patients with T2DM. CONCLUSIONS: This study suggests that T2DM may accelerate neurovascular coupling impairment in specific brain regions (the left insula), contributing to memory decline. This study implies that the mReHo:mCBF ratio is a potential imaging marker for detecting neurovascular changes. BMJ Publishing Group 2021-01-18 /pmc/articles/PMC7816934/ /pubmed/33462074 http://dx.doi.org/10.1136/bmjdrc-2020-001433 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Pathophysiology/Complications
Zhang, Yang
Zhang, Xiaolu
Ma, Guangyang
Qin, Wen
Yang, Jiayang
Lin, Jiahui
Zhang, Quan
Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study
title Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study
title_full Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study
title_fullStr Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study
title_full_unstemmed Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study
title_short Neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal MRI study
title_sort neurovascular coupling alterations in type 2 diabetes: a 5-year longitudinal mri study
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816934/
https://www.ncbi.nlm.nih.gov/pubmed/33462074
http://dx.doi.org/10.1136/bmjdrc-2020-001433
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