A paleo-neurologic investigation of the social brain hypothesis in frontotemporal dementia

Author:

Vandenbulcke Mathieu12,Van de Vliet Laura1,Sun Jiaze1,Huang Yun-An1,Van Den Bossche Maarten J A12,Sunaert Stefan34,Peeters Ron34,Zhu Qi5,Vanduffel Wim567,de Gelder Beatrice8910,De Winter François-Laurent12,Van den Stock Jan12

Affiliation:

1. Neuropsychiatry, Leuven Brain Institute , KU Leuven, Leuven 3000 , Belgium

2. Geriatric Psychiatry, University Psychiatric Center KU Leuven , Leuven 3000 , Belgium

3. Department of Radiology, University Hospitals Leuven , Leuven 3000 , Belgium

4. Department of Imaging and Pathology, KU Leuven , Leuven 3000 , Belgium

5. Laboratory for Neuro- and Psychophysiology, Leuven Brain Institute , KU Leuven, Leuven 3000 , Belgium

6. Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital , Charlestown, MA 02129 , USA

7. Department of Radiology, Harvard Medical School , Boston, MA 02144 , USA

8. Department of Cognitive Neuroscience , Faculty of Psychology and Neuroscience, , Maastricht 6229 EV , The Netherlands

9. Maastricht University , Faculty of Psychology and Neuroscience, , Maastricht 6229 EV , The Netherlands

10. Department of Computer Science, University College London , London WC1E 6BT , UK

Abstract

Abstract The social brain hypothesis posits that a disproportionate encephalization in primates enabled to adapt behavior to a social context. Also, it has been proposed that phylogenetically recent brain areas are disproportionally affected by neurodegeneration. Using structural and functional magnetic resonance imaging, the present study investigates brain–behavior associations and neural integrity of hyperspecialized and domain-general cortical social brain areas in behavioral variant frontotemporal dementia (bvFTD). The results revealed that both structure and function of hyperspecialized social areas in the middle portion of the superior temporal sulcus (STS) are compromised in bvFTD, while no deterioration was observed in domain general social areas in the posterior STS. While the structural findings adhered to an anterior–posterior gradient, the functional group differences only occurred in the hyperspecialized locations. Activity in specialized regions was associated with structural integrity of the amygdala and with social deficits in bvFTD. In conclusion, the results are in line with the paleo-neurology hypothesis positing that neurodegeneration primarily hits cortical areas showing increased specialization, but also with the compatible alternative explanation that anterior STS regions degenerate earlier, based on stronger connections to and trans-neuronal spreading from regions affected early in bvFTD.

Funder

KU Leuven

Fonds Wetenschappelijk Onderzoek

Sequoia Fund for Research on Aging and Mental Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

同舟云学术

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

"同舟云学术"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,当前同舟云学术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 © 2019-2024 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