Shared and differing functional connectivity abnormalities of the default mode network in mild cognitive impairment and Alzheimer’s disease

楔前 默认模式网络 后扣带 角回 神经科学 前额叶皮质 扣带回前部 认知 心理学
作者
Yaxuan Wang,Qian Li,Yao Li,Ning He,Yingying Tang,Lizhou Chen,Fenghua Long,Yufei Chen,Graham J. Kemp,Su Lui,Fei Li
出处
期刊:Cerebral Cortex [Oxford University Press]
卷期号:34 (3) 被引量:41
标识
DOI:10.1093/cercor/bhae094
摘要

Abstract Alzheimer’s disease (AD) and mild cognitive impairment (MCI) both show abnormal resting-state functional connectivity (rsFC) of default mode network (DMN), but it is unclear to what extent these abnormalities are shared. Therefore, we performed a comprehensive meta-analysis, including 31 MCI studies and 20 AD studies. MCI patients, compared to controls, showed decreased within-DMN rsFC in bilateral medial prefrontal cortex/anterior cingulate cortex (mPFC/ACC), precuneus/posterior cingulate cortex (PCC), right temporal lobes, and left angular gyrus and increased rsFC between DMN and left inferior temporal gyrus. AD patients, compared to controls, showed decreased rsFC within DMN in bilateral mPFC/ACC and precuneus/PCC and between DMN and left inferior occipital gyrus and increased rsFC between DMN and right dorsolateral prefrontal cortex. Conjunction analysis showed shared decreased rsFC in mPFC/ACC and precuneus/PCC. Compared to MCI, AD had decreased rsFC in left precuneus/PCC and between DMN and left inferior occipital gyrus and increased rsFC in right temporal lobes. MCI and AD share a decreased within-DMN rsFC likely underpinning episodic memory deficits and neuropsychiatric symptoms, but differ in DMN rsFC alterations likely related to impairments in other cognitive domains such as language, vision, and execution. This may throw light on neuropathological mechanisms in these two stages of dementia.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
小菜完成签到,获得积分10
1秒前
1秒前
2秒前
2秒前
3秒前
3秒前
5秒前
嗨害害发布了新的文献求助10
5秒前
水夜完成签到,获得积分10
5秒前
6秒前
6秒前
田様应助季春九采纳,获得10
7秒前
小马发布了新的文献求助10
7秒前
善学以致用应助刘明生采纳,获得10
8秒前
8秒前
城九寒发布了新的文献求助10
9秒前
10秒前
天天快乐应助JamesTYD采纳,获得10
11秒前
一个左正蹬完成签到,获得积分10
13秒前
MIYA完成签到 ,获得积分10
13秒前
lanlan完成签到 ,获得积分10
15秒前
16秒前
17秒前
英姑应助小马采纳,获得10
17秒前
标致的帽子完成签到,获得积分10
18秒前
朱gui发布了新的文献求助10
18秒前
水夜发布了新的文献求助10
18秒前
微凉发布了新的文献求助10
20秒前
dxszing完成签到 ,获得积分10
20秒前
21秒前
21秒前
21秒前
Mitty完成签到 ,获得积分10
22秒前
赘婿应助念安采纳,获得10
22秒前
22秒前
搜集达人应助毅诚菌采纳,获得30
22秒前
零点起步完成签到,获得积分10
22秒前
23秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Metallurgy at high pressures and high temperatures 2000
Inorganic Chemistry Eighth Edition 1200
High Pressures-Temperatures Apparatus 1000
Free parameter models in liquid scintillation counting 1000
Standards for Molecular Testing for Red Cell, Platelet, and Neutrophil Antigens, 7th edition 1000
The Organic Chemistry of Biological Pathways Second Edition 800
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6323640
求助须知:如何正确求助?哪些是违规求助? 8140058
关于积分的说明 17065929
捐赠科研通 5376669
什么是DOI,文献DOI怎么找? 2853647
邀请新用户注册赠送积分活动 1831305
关于科研通互助平台的介绍 1682506