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      Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages

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          Abstract

          Objective

          Consistent with the cognitive reserve hypothesis, higher education and occupation attainments may help persons with neurodegenerative dementias to better withstand neuropathology before developing cognitive impairment. We tested here the cognitive reserve hypothesis in patients with frontotemporal dementia (FTD), with or without pathogenetic granulin mutations ( GRN+ and GRN-), and in presymptomatic GRN mutation carriers ( aGRN+) .

          Methods

          Education and occupation attainments were assessed and combined to define Reserve Index (RI) in 32 FTD patients, i.e. 12 GRN+ and 20 GRN-, and in 17 aGRN+. Changes in functional connectivity were estimated by resting state fMRI, focusing on the salience network (SN), executive network (EN) and bilateral frontoparietal networks (FPNs). Cognitive status was measured by FTD-modified Clinical Dementia Rating Scale.

          Results

          In FTD patients higher level of premorbid cognitive reserve was associated with reduced connectivity within the SN and the EN. EN was more involved in FTD patients without GRN mutations, while SN was more affected in GRN pathology. In aGRN+, cognitive reserve was associated with reduced SN.

          Conclusions

          This study suggests that cognitive reserve modulates functional connectivity in patients with FTD, even in monogenic disease. In GRN inherited FTD, cognitive reserve mechanisms operate even in presymptomatic to clinical stages.

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          Most cited references16

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          The frontoparietal attention network of the human brain: action, saliency, and a priority map of the environment.

          Radek Ptak (2012)
          The dorsal convexity of the human frontal and parietal lobes forms a network that is crucially involved in the selection of sensory contents by attention. This network comprehends cortex along the intraparietal sulcus, the inferior parietal lobe, and dorsal premotor cortex, including the frontal eye field. These regions are richly interconnected with recurrent fibers passing through the superior longitudinal fasciculus. The posterior parietal cortex has several functional characteristics-such as feature-independent coding, enhancement of activity by attention, representation of task-related signals, and access to multiple reference frames-that point to a central role of this region in the computation of a feature- and modality-independent priority map of the environment. The priority map integrates feature information elaborated in sensory cortex and top-down representations of behavioral goals and expectations originating in the dorsolateral prefrontal and premotor cortex. This review presents converging evidence from single-unit studies of the primate brain, functional neuroimaging, and investigations of neuropsychological disorders such as Bálint syndrome and spatial neglect for a decisive role of the frontoparietal attention network in the selection of relevant environmental information.
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            Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease.

            An international group of clinical and basic scientists participated in the Frontotemporal Dementia and Pick's Disease Criteria Conference at the National Institutes of Health in Bethesda, Md, on July 7, 2000, to reassess clinical and neuropathological criteria for the diagnosis of frontotemporal dementia (FTD). Previous criteria for FTD have primarily been designed for research purposes. The goal of this meeting was to propose guidelines that would enable clinicians (particularly neurologists, psychiatrists, and neuropsychologists) to recognize patients with FTD and, if appropriate, to expedite their referral to a diagnostic center. In addition, recommendations for the neuropathological criteria of FTD were reviewed, relative to classical neuropathology and modern molecular biology.
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              Regional brain atrophy and functional disconnection across Alzheimer's disease evolution.

              To assess the contribution of regional grey matter (GM) atrophy and functional disconnection in determining the level of cognitive decline in patients with Alzheimer's disease (AD) at different clinical stages. Ten patients with amnesic mild cognitive impairment (a-MCI), 11 patients with probable AD and 10 healthy controls were recruited. T1 volumes were obtained from each subject and postprocessed according to an optimised voxel based morphometry protocol. Resting state functional MRI data were also collected from the same individuals and analysed to produce connectivity maps after identification of the default mode network (DMN) by independent component analysis. Compared with healthy controls, both AD and a-MCI patients showed a similar regional pattern of brain disconnection between the posterior cingulate cortex (PCC) and the medial prefrontal cortex and the rest of the brain. Conversely, the distribution of GM atrophy was significantly more restricted in a-MCI than in AD patients. Interestingly, the PCC showed reduced connectivity in a-MCI patients in the absence of GM atrophy, which was, in contrast, detectable at the stage of fully developed AD. This study indicates that disconnection precedes GM atrophy in the PCC, which is a critical area of the DMN, and supports the hypothesis that GM atrophy in specific regions of AD brains likely reflects a long term effect of brain disconnection. In this context, our study indicates that GM atrophy in PCC accompanies the conversion from MCI to AD.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                9 September 2013
                : 8
                : 9
                : e74762
                Affiliations
                [1 ]Centre for Neurodegenerative Disorders, University of Brescia, Brescia, Italy
                [2 ]Neuroimaging Laboratory, Santa Lucia Foundation IRCCS, Rome, Italy
                [3 ]III Laboratory of Analysis, Brescia Hospital, Brescia, Italy
                [4 ]Brighton and Sussex Medical School, Clinical Imaging Centre, University of Sussex, Brighton, United Kingdom
                [5 ]Geriatric Research Group, Brescia, Italy
                [6 ]Neuroradiology Unit, University of Brescia, Brescia, Italy
                [7 ]Neurology Unit, ValleCamonica Hospital, Brescia, Italy
                [8 ]Department of Neuroscience, University of Rome “Tor Vergata”, Rome, Italy
                University G. D'Annunzio, Italy
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: EP BB. Performed the experiments: EP SG MB MC. Analyzed the data: EP SG. Contributed reagents/materials/analysis tools: RG SA. Wrote the manuscript: EP SG BB MB AA AB MT CC AP.

                Article
                PONE-D-13-24749
                10.1371/journal.pone.0074762
                3767639
                24040338
                26f09e7c-5ea3-4e4e-9de8-9898d1ffff63
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 15 June 2013
                : 2 August 2013
                Funding
                The authors have no funding or support to report.
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                Research Article

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