Stepwise Functional Brain Architecture Correlates with Atrophy in Progressive Supranuclear Palsy

进行性核上麻痹 萎缩 中脑 神经科学 医学 心理学 病理 中枢神经系统
作者
Edoardo Gioele Spinelli,Alma Ghirelli,Ilaria Bottale,Silvia Basaia,Elisa Canu,Veronica Castelnovo,Maria Antonietta Volonté,Sebastiano Galantucci,Giuseppe Magnani,Francesca Caso,Giordano Cecchetti,Paola Caroppo,Sara Prioni,Cristina Villa,Keith A. Josephs,Jennifer L. Whitwell,Massimo Filippi,Federica Agosta
出处
期刊:Movement Disorders [Wiley]
卷期号:39 (9): 1493-1503 被引量:1
标识
DOI:10.1002/mds.29887
摘要

Abstract Background Stepwise functional connectivity (SFC) detects whole‐brain functional couplings of a selected region of interest at increasing link‐step topological distances. Objective This study applied SFC to test the hypothesis that stepwise architecture propagating from the disease epicenter would shape patterns of brain atrophy in patients with progressive supranuclear palsy–Richardson's syndrome (PSP‐RS). Methods Thirty‐six patients with PSP‐RS and 44 age‐matched healthy control subjects underwent brain magnetic resonance imaging on a 3‐T scanner. The disease epicenter was defined as the peak of atrophy observed in an independent cohort of 13 cases with postmortem confirmation of PSP pathology and used as seed region for SFC analysis. First, we explored SFC rearrangements in patients with PSP‐RS, as compared with age‐matched control subjects. Subsequently, we tested SFC architecture propagating from the disease epicenter as a determinant of brain atrophy distribution. Results The disease epicenter was identified in the left midbrain tegmental region. Compared with age‐matched control subjects, patients with PSP‐RS showed progressively widespread decreased SFC of the midbrain with striatal and cerebellar regions through direct connections and sensorimotor cortical regions through indirect connections. A correlation was found between average link‐step distance from the left midbrain in healthy subjects and brain volumes in patients with PSP‐RS ( r = 0.38, P < 0.001). Conclusions This study provides comprehensive insights into the topology of functional network rearrangements in PSP‐RS and demonstrates that the brain architectural topology, as described by SFC propagating from the disease epicenter, shapes the pattern of atrophic changes in PSP‐RS. Our findings support the view of a network‐based pathology propagation in this primary tauopathy. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
雷雷完成签到,获得积分10
1秒前
HSA发布了新的文献求助10
2秒前
霸气以菱发布了新的文献求助10
4秒前
领导范儿应助小雒雒采纳,获得10
5秒前
斯文冷亦完成签到 ,获得积分10
8秒前
10秒前
10秒前
11秒前
11秒前
12秒前
12秒前
李健的小迷弟应助小安采纳,获得10
13秒前
妮儿发布了新的文献求助10
13秒前
哒哒哒发布了新的文献求助10
15秒前
淡淡代玉发布了新的文献求助20
15秒前
小袁完成签到,获得积分10
15秒前
等待冰露发布了新的文献求助10
16秒前
huangbaba11完成签到 ,获得积分0
16秒前
迷人成协发布了新的文献求助10
16秒前
小雒雒发布了新的文献求助10
17秒前
传奇3应助阿邱采纳,获得10
21秒前
ZONG完成签到,获得积分10
23秒前
哒哒哒完成签到,获得积分10
23秒前
24秒前
25秒前
26秒前
阿明完成签到,获得积分10
27秒前
28秒前
NMR发布了新的文献求助10
30秒前
32秒前
乐观小蕊完成签到 ,获得积分10
33秒前
无花果应助shiyu Fang采纳,获得10
33秒前
luoyujia完成签到,获得积分10
33秒前
wing00024完成签到,获得积分10
37秒前
阿邱发布了新的文献求助10
37秒前
sia发布了新的文献求助10
37秒前
39秒前
任性的静枫完成签到,获得积分10
39秒前
领导范儿应助科研通管家采纳,获得10
40秒前
慕青应助科研通管家采纳,获得20
40秒前
高分求助中
The Mother of All Tableaux: Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 3000
A new approach to the extrapolation of accelerated life test data 1000
Problems of point-blast theory 400
Indomethacinのヒトにおける経皮吸収 400
北师大毕业论文 基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 390
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
Robot-supported joining of reinforcement textiles with one-sided sewing heads 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3997679
求助须知:如何正确求助?哪些是违规求助? 3537190
关于积分的说明 11270985
捐赠科研通 3276344
什么是DOI,文献DOI怎么找? 1806900
邀请新用户注册赠送积分活动 883582
科研通“疑难数据库(出版商)”最低求助积分说明 809975