4.7 Article

Locating Temporal Functional Dynamics of Visual Short-Term Memory Binding using Graph Modular Dirichlet Energy

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SCIENTIFIC REPORTS
卷 7, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/srep42013

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资金

  1. Engineering and Physical Sciences Research Council (UK) via a DTP studentship [EP/N014421/1]
  2. Royal Society of Edinburgh
  3. SNF [200021 154350/1]
  4. CONICET
  5. FONCyT-PICT [2012-1309, 2012-0412]
  6. FONDAP [15150012]
  7. INECO Foundation
  8. Alzheimer's Society [AS-R42303]
  9. MRC [MRC-R42552]
  10. Alzheimer's Scotland Dementia Research
  11. Centre for Cognitive Ageing and Cognitive Epidemiology part of the cross council Lifelong Health from the University of Edinburgh
  12. Wellbeing Initiative from the University of Edinburgh [MR/K026992/1]
  13. CONICYT/FONDECYT Regular [1130920]
  14. EPSRC [EP/N014421/1] Funding Source: UKRI
  15. Engineering and Physical Sciences Research Council [EP/N014421/1, 1647466] Funding Source: researchfish
  16. Medical Research Council [MR/K026992/1] Funding Source: researchfish

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Visual short-term memory binding tasks are a promising early marker for Alzheimer's disease (AD). To uncover functional deficits of AD in these tasks it is meaningful to first study unimpaired brain function. Electroencephalogram recordings were obtained from encoding and maintenance periods of tasks performed by healthy young volunteers. We probe the task's transient physiological underpinnings by contrasting shape only (Shape) and shape-colour binding (ind) conditions, displayed in the left and right sides of the screen, separately. Particularly, we introduce and implement a novel technique named Modular Dirichlet Energy (MDE) which allows robust and flexible analysis of the functional network with unprecedented temporal precision. We find that connectivity in the Bind condition is less integrated with the global network than in the Shape condition in occipital and frontal modules during the encoding period of the right screen condition. Using MDE we are able to discern driving effects in the occipital module between 100-140 ms, coinciding with the P100 visually evoked potential, followed by a driving effect in the frontal module between 140-180 ms, suggesting that the differences found constitute an information processing difference between these modules. This provides temporally precise information over a heterogeneous population in promising tasks for the detection of AD.

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