Intra‐ and inter‐network functional alterations in <scp>P</scp>arkinson's disease with mild cognitive impairment

  • Luis R. Peraza
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • David Nesbitt
    Medical Research Council Cognition and Brain Sciences Unit, University of Cambridge Cambridge CB2 7EF United Kingdom
  • Rachael A. Lawson
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • Gordon W. Duncan
    Centre for Clinical Brain Sciences, University of Edinburgh Edinburgh United Kingdom
  • Alison J. Yarnall
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • Tien K. Khoo
    School of Medicine and Menzies Health Institute Queensland, Griffith University QLD 4222 Australia
  • Marcus Kaiser
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • Michael J. Firbank
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • John T. O'Brien
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • Roger A. Barker
    John van Geest Centre for Brain Repair, University of Cambridge Cambridge CB2 0PY United Kingdom
  • David J. Brooks
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • David J. Burn
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom
  • John‐Paul Taylor
    Institute of Neuroscience, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne NE4 5PL United Kingdom

抄録

<jats:title>Abstract</jats:title><jats:p>Mild cognitive impairment (MCI) is prevalent in 15%–40% of Parkinson's disease (PD) patients at diagnosis. In this investigation, we study brain intra‐ and inter‐network alterations in resting state functional magnetic resonance imaging (rs‐fMRI) in recently diagnosed PD patients and characterise them as either cognitive normal (PD‐NC) or with MCI (PD‐MCI). Patients were divided into two groups, PD‐NC (<jats:italic>N</jats:italic> = 62) and PD‐MCI (<jats:italic>N</jats:italic> = 37) and for comparison, healthy controls (HC, <jats:italic>N</jats:italic> = 30) were also included. Intra‐ and inter‐network connectivity were investigated from participants’ rs‐fMRIs in 26 resting state networks (RSNs). Intra‐network differences were found between both patient groups and HCs for networks associated with motor control (motor cortex), spatial attention and visual perception. When comparing both PD‐NC and PD‐MCI, intra‐network alterations were found in RSNs related to attention, executive function and motor control (cerebellum). The inter‐network analysis revealed a hyper‐synchronisation between the basal ganglia network and the motor cortex in PD‐NC compared with HCs. When both patient groups were compared, intra‐network alterations in RSNs related to attention, motor control, visual perception and executive function were found. We also detected disease‐driven negative synchronisations and synchronisation shifts from positive to negative and vice versa in both patient groups compared with HCs. The hyper‐synchronisation between basal ganglia and motor cortical RSNs in PD and its synchronisation shift from negative to positive compared with HCs, suggest a compensatory response to basal dysfunction and altered basal‐cortical motor control in the resting state brain of PD patients. <jats:italic>Hum Brain Mapp 38:1702–1715, 2017</jats:italic>. © 2016 Wiley Periodicals, Inc.</jats:p>

収録刊行物

被引用文献 (2)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ