Impaired theta phase coupling underlies frontotemporal dysconnectivity in schizophrenia

Author:

Adams Rick A12345ORCID,Bush Daniel16,Zheng Fanfan17,Meyer Sofie S16,Kaplan Raphael58,Orfanos Stelios910,Marques Tiago Reis1112,Howes Oliver D1112,Burgess Neil156

Affiliation:

1. Institute of Cognitive Neuroscience, University College London, 17 Queen Square, London, WC1N 3AZ, UK

2. Division of Psychiatry, University College London, 149 Tottenham Court Road, London, W1T 7NF, UK

3. Max Planck-UCL Centre for Computational Psychiatry and Ageing Research, 10-12 Russell Square, London, WC1B 5EH, UK

4. Centre for Medical Image Computing, Department of Computer Science, University College London, Malet Place, London, WC1E 7JE, UK

5. Wellcome Centre for Human Neuroimaging, University College London, 12 Queen Square, London, WC1N 3BG, UK

6. Queen Square Institute of Neurology, University College London, London, WC1N 3BG, UK

7. Brainnetome Center, Institute of Automation, Chinese Academy of Sciences, 95 Zhongguancun East Road, 100190 Beijing, China

8. Kavli Institute for Systems Neuroscience, Norwegian University of Science and Technology, Trondheim, Norway

9. South West London and St George’s Mental Health NHS Trust, Springfield University Hospital, 61 Glenburnie Rd, London SW17 7DJ, UK

10. Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology, and Neuroscience, King’s College London, De Crespigny Park, Denmark Hill, London SE5 8AF, UK

11. Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, Hammersmith Hospital, London, W12 0NN, UK

12. Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King’s College London, London, SE5 8AF, UK

Abstract

Abstract Frontotemporal dysconnectivity is a key pathology in schizophrenia. The specific nature of this dysconnectivity is unknown, but animal models imply dysfunctional theta phase coupling between hippocampus and medial prefrontal cortex (mPFC). We tested this hypothesis by examining neural dynamics in 18 participants with a schizophrenia diagnosis, both medicated and unmedicated; and 26 age, sex and IQ matched control subjects. All participants completed two tasks known to elicit hippocampal-prefrontal theta coupling: a spatial memory task (during magnetoencephalography) and a memory integration task. In addition, an overlapping group of 33 schizophrenia and 29 control subjects underwent PET to measure the availability of GABAARs expressing the α5 subunit (concentrated on hippocampal somatostatin interneurons). We demonstrate—in the spatial memory task, during memory recall—that theta power increases in left medial temporal lobe (mTL) are impaired in schizophrenia, as is theta phase coupling between mPFC and mTL. Importantly, the latter cannot be explained by theta power changes, head movement, antipsychotics, cannabis use, or IQ, and is not found in other frequency bands. Moreover, mPFC-mTL theta coupling correlated strongly with performance in controls, but not in subjects with schizophrenia, who were mildly impaired at the spatial memory task and no better than chance on the memory integration task. Finally, mTL regions showing reduced phase coupling in schizophrenia magnetoencephalography participants overlapped substantially with areas of diminished α5-GABAAR availability in the wider schizophrenia PET sample. These results indicate that mPFC-mTL dysconnectivity in schizophrenia is due to a loss of theta phase coupling, and imply α5-GABAARs (and the cells that express them) have a role in this process.

Funder

MRC Skills Development Fellow

Academy of Medical Sciences

National Institute of Health Research

NIHR

UCLH Biomedical Research Centre

Sir Henry Wellcome

Medical Research Council UK

Maudsley Charity

Brain and Behavior Research Foundation

Wellcome Trust

Wellcome Principal Research Fellow

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

全球学者库

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"全球学者库"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前全球学者库共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2023 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3