Literature DB >> 19847048

Pinpointing synaptic loss caused by Alzheimer's disease with fMRI.

Adam M Brickman1, Scott A Small, Adam Fleisher.   

Abstract

During its earliest stage, before cell loss and independent of amyloid plaques and neurofibrillary tangles, Alzheimer's disease (AD) causes synaptic loss affecting the basal functional properties of neurons. In principle, synaptic loss can be detected by measuring AD-induced changes in basal function, or by measuring stimulus-evoked responses on top of basal changes. Functional magnetic resonance imaging (fMRI) is sensitive to both basal changes and evoked-responses, and there are therefore two experimental approaches in which fMRI can be used to pinpoint synaptic loss in AD. In this review, we will compare and contrast both approaches for pinpointing when and where synaptic loss in AD begins and for monitoring therapeutic efficacy.

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Year:  2009        PMID: 19847048      PMCID: PMC2857999          DOI: 10.3233/BEN-2009-0240

Source DB:  PubMed          Journal:  Behav Neurol        ISSN: 0953-4180            Impact factor:   3.342


  30 in total

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5.  Imaging correlates of brain function in monkeys and rats isolates a hippocampal subregion differentially vulnerable to aging.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-26       Impact factor: 11.205

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7.  Focal physiological uncoupling of cerebral blood flow and oxidative metabolism during somatosensory stimulation in human subjects.

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8.  Functional MR imaging in Alzheimer's disease during memory encoding.

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9.  High-level neuronal expression of abeta 1-42 in wild-type human amyloid protein precursor transgenic mice: synaptotoxicity without plaque formation.

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3.  The ModRey: An Episodic Memory Test for Nonclinical and Preclinical Populations.

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4.  Hemodynamic and metabolic correspondence of resting-state voxel-based physiological metrics in healthy adults.

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Review 6.  A review of β-amyloid neuroimaging in Alzheimer's disease.

Authors:  Paul A Adlard; Bob A Tran; David I Finkelstein; Patricia M Desmond; Leigh A Johnston; Ashley I Bush; Gary F Egan
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7.  Neuronal hyperactivity due to loss of inhibitory tone in APOE4 mice lacking Alzheimer's disease-like pathology.

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Journal:  Nat Commun       Date:  2017-11-13       Impact factor: 14.919

  7 in total

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