Reduced functional brain connectivity prior to and after disease onset in Huntington's disease

被引:50
|
作者
Dumas, Eve M. [1 ]
van den Bogaard, Simon J. A. [1 ]
Hart, Ellen P. [1 ]
Soeter, Roelof P. [2 ]
van Buchem, Mark A. [2 ]
van der Grond, Jeroen [2 ]
Rombouts, Serge A. R. B. [2 ,3 ,4 ]
Roos, Raymund A. C. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Neurol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Radiol, NL-2300 RC Leiden, Netherlands
[3] Leiden Univ, Inst Psychol, NL-2300 RC Leiden, Netherlands
[4] LIBC, Leiden, Netherlands
关键词
Huntington's disease; Resting state fMRI; Premanifest gene carriers; Functional connectivity; PREFRONTAL CORTEX; DYSFUNCTION; MRI; PROGRESSION; PATHOLOGY; NETWORKS; ATROPHY; ROBUST; ADULTS; MODEL;
D O I
10.1016/j.nicl.2013.03.001
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
Background: Huntington's disease (HD) is characterised by both regional and generalised neuronal cell loss in the brain. Investigating functional brain connectivity patterns in rest in HD has the potential to broaden the understanding of brain functionality in relation to disease progression. This study aims to establish whether brain connectivity during rest is different in premanifest and manifest HD as compared to controls. Methods: At the Leiden University Medical Centre study site of the TRACK-HD study, 20 early HD patients (disease stages 1 and 2), 28 premanifest gene carriers and 28 healthy controls underwent 3 T MRI scanning. Standard and high-resolution T1-weighted images and a resting state fMRI scan were acquired. Using FSL, group differences in resting state connectivity were examined for eight networks of interest using a dual regression method. With a voxel wise correction for localised atrophy, group differences in functional connectivity were examined. Results: Brain connectivity of the left middle frontal and pre-central gyrus, and right post central gyrus with the medial visual network was reduced in premanifest and manifest HD as compared to controls (0.05 > p > 0.0001). In manifest HD connectivity of numerous widespread brain regions with the default mode network and the executive control network were reduced (0.05 > p > 0.0001). Discussion: Brain regions that show reduced intrinsic functional connectivity are present in premanifest gene carriers and to a much larger extent in manifest HD patients. These differences are present even when the potential influence of atrophy is taken into account. Resting state fMRI could potentially be used for early disease detection in the premanifest phase of HD and for monitoring of disease modifying compounds. (C) 2013 The Authors. Published by Elsevier Inc. Open access under CC BY license.
引用
收藏
页码:377 / 384
页数:8
相关论文
共 50 条
  • [41] Statin use and delayed onset of Huntington's disease
    Schultz, Jordan L.
    Nopoulos, Peg C.
    Killoran, Annie
    Kamholz, John A.
    MOVEMENT DISORDERS, 2019, 34 (02) : 281 - 285
  • [42] A critical review of brain and cognitive reserve in Huntington's disease
    Soloveva, Maria V.
    Jamadar, Sharna D.
    Poudel, Govinda
    Georgiou-Karistianis, Nellie
    NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2018, 88 : 155 - 169
  • [43] Structural and Metabolic Brain Correlates of Apathy in Huntington's Disease
    Martinez-Horta, Saul
    Perez-Perez, Jesus
    Sampedro, Frederic
    Pagonabarraga, Javier
    Horta-Barba, Andrea
    Carceller-Sindreu, Mar
    Gomez-Anson, Beatriz
    Andrea Lozano-Martinez, Gloria
    Alfonso Lopez-Mora, Diego
    Camacho, Valle
    Fernandez-Leon, Alejandro
    Carrio, Ignasi
    Kulisevsky, Jaime
    MOVEMENT DISORDERS, 2018, 33 (07) : 1151 - 1159
  • [44] Neurophysiological hallmarks of Huntington's disease progression: an EEG and fMRI connectivity study
    Ponomareva, Natalya V.
    Klyushnikov, Sergey A.
    Abramycheva, Natalia
    Konovalov, Rodion N.
    Krotenkova, Marina
    Kolesnikova, Ekaterina
    Malina, Daria
    Urazgildeeva, Gusel
    Kanavets, Elena
    Mitrofanov, Andrey
    Fokin, Vitaly
    Rogaev, Evgeny
    Illarioshkin, Sergey N.
    FRONTIERS IN AGING NEUROSCIENCE, 2023, 15
  • [45] Onset of Huntington's Disease: Can It Be Purely Cognitive?
    Paulsen, Jane S.
    Long, Jeffrey D.
    MOVEMENT DISORDERS, 2014, 29 (11) : 1342 - 1350
  • [46] Differential Changes in Functional Connectivity of Striatum-Prefrontal and Striatum-Motor Circuits in Premanifest Huntington's Disease
    Kronenbuerger, Martin
    Hua, Jun
    Bang, Jee Y. A.
    Ultz, Kia E.
    Miao, Xinyuan
    Zhang, Xiaoyu
    Pekar, James J.
    van Zijl, Peter C. M.
    Duan, Wenzhen
    Margolis, Russell L.
    Ross, Christopher A.
    NEURODEGENERATIVE DISEASES, 2019, 19 (02) : 78 - 87
  • [47] Functional and connectivity changes during working memory in Huntington's disease: 18 month longitudinal data from the IMAGE-HD study
    Georgiou-Karistianis, Nellie
    Poudel, Govinda R.
    Dominguez, Juan F. D.
    Langmaid, Rebecca
    Gray, Marcus A.
    Churchyard, Andrew
    Chua, Phyllis
    Borowsky, Beth
    Egan, Gary F.
    Stout, Julie C.
    BRAIN AND COGNITION, 2013, 83 (01) : 80 - 91
  • [48] A study of neural activity and functional connectivity within the olfactory brain network in Parkinson's disease
    Georgiopoulos, Charalampos
    Witt, Suzanne T.
    Haller, Sven
    Dizdar, Nil
    Zachrisson, Helene
    Engstrom, Maria
    Larsson, Elna-Marie
    NEUROIMAGE-CLINICAL, 2019, 23
  • [49] Age at onset reveals different functional connectivity abnormalities in prodromal Alzheimer’s disease
    Lorenzo Pini
    Cristina Geroldi
    Samantha Galluzzi
    Roberta Baruzzi
    Monica Bertocchi
    Eugenia Chitò
    Stefania Orini
    Melissa Romano
    Maria Cotelli
    Sandra Rosini
    Silvia Magnaldi
    Mauro Morassi
    Milena Cobelli
    Cristian Bonvicini
    Silvana Archetti
    Orazio Zanetti
    Giovanni B. Frisoni
    Michela Pievani
    Brain Imaging and Behavior, 2020, 14 : 2594 - 2605
  • [50] Evolution of brain gray matter loss in Huntington's disease: a meta-analysis
    Lambrecq, V.
    Langbour, N.
    Guehl, D.
    Bioulac, B.
    Burbaud, P.
    Rotge, J. -Y.
    EUROPEAN JOURNAL OF NEUROLOGY, 2013, 20 (02) : 315 - 321