• Kamil A Grajski, Steven L Bressler, and Alzheimer's Disease Neuroimaging Initiative.
• NuroSci, LLC., West Palm Beach, FL 33401, USA. Electronic address: kgrajski@nurosci.com.
• Neuroimage Clin. 2019 Jan 1; 23: 101860.

AbstractWe report group level differential detection of medial temporal lobe resting-state functional connectivity disruption and morphometric changes in the transition from cognitively normal to early mild cognitive impairment in an age-, education- and gender-matched 105 subjects Alzheimer's Disease Neuroimaging Initiative dataset. In mild Alzheimer's Disease, but not early mild cognitive impairment, characteristic brain atrophy was detected in FreeSurfer estimates of subcortical and hippocampal subfield volumes and cortical thinning. By contrast, functional connectivity analysis detected earlier significant changes. In early mild cognitive impairment these changes involved medial temporal lobe regions of transentorhinal, perirhinal and entorhinal cortices (associated with the earliest stages of neurofibrillary changes in Alzheimer's Disease), hippocampus, parahippocampal gyrus and temporal pole, and cortical regions comprising or co-activated with the default-mode network, including rostral and medial prefrontal cortex, anterior cingulate cortex, precuneus and inferior temporal cortex. Key findings include: a) focal, bilaterally symmetric spatial organization of affected medial temporal lobe regions; b) mutual hyperconnectivity involving ventral medial temporal lobe structures (temporal pole, uncus); c) dorsal medial temporal lobe hypoconnectivity with anterior and posterior midline default-mode network nodes; and d) a complex pattern of transient and persistent changes in hypo- and hyper-connectivity across Alzheimer's Disease stages. These findings position medial temporal lobe resting state functional connectivity as a candidate biomarker of an Alzheimer's Disease pathophysiological cascade, potentially in advance of clinical biomarkers, and coincident with biomarkers of the earliest stages of Alzheimer's neuropathology.Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

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