Tackling variability: A multicenter study to provide a gold-standard network approach for frontotemporal dementia

Biomarkers represent a critical research area in neurodegeneration disease as they can contribute to studying potential disease-modifying agents, fostering timely therapeutic interventions, and alleviating associated financial costs. Functional connectivity (FC) analysis represents a promising appro...

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Autor principal: Sedeño, L.
Otros Autores: Piguet, O., Abrevaya, S., Desmaras, H., García-Cordero, I., Baez, S., Alethia de la Fuente, L., Reyes, P., Tu, S., Moguilner, S., Lori, N., Landin-Romero, R., Matallana, D., Slachevsky, A., Torralva, T., Chialvo, D., Kumfor, F., García, A.M, Manes, F., Hodges, J.R, Ibanez, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: John Wiley and Sons Inc. 2017
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Acceso en línea:Registro en Scopus
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100 1 |a Sedeño, L. 
245 1 0 |a Tackling variability: A multicenter study to provide a gold-standard network approach for frontotemporal dementia 
260 |b John Wiley and Sons Inc.  |c 2017 
270 1 0 |m Ibanez, A.; Institute of Cognitive and Translational Neuroscience (INCyT), INECO Foundation, Favaloro UniversityArgentina; email: aibanez@ineco.org.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Biomarkers represent a critical research area in neurodegeneration disease as they can contribute to studying potential disease-modifying agents, fostering timely therapeutic interventions, and alleviating associated financial costs. Functional connectivity (FC) analysis represents a promising approach to identify early biomarkers in specific diseases. Yet, virtually no study has tested whether potential FC biomarkers prove to be reliable and reproducible across different centers. As such, their implementation remains uncertain due to multiple sources of variability across studies: the numerous international centers capable conducting FC research vary in their scanning equipment and their samples’ socio-cultural background, and, more troublingly still, no gold-standard method exists to analyze FC. In this unprecedented study, we aim to address both issues by performing the first multicenter FC research in the behavioral-variant frontotemporal dementia (bvFTD), and by assessing multiple FC approaches to propose a gold-standard method for analysis. We enrolled 52 bvFTD patients and 60 controls from three international clinics (with different fMRI recording parameters), and three additional neurological patient groups. To evaluate FC, we focused on seed analysis, inter-regional connectivity, and several graph-theory approaches. Only graph-theory analysis, based on weighted-matrices, yielded consistent differences between bvFTD and controls across centers. Also, graph metrics robustly discriminated bvFTD from the other neurological conditions. The consistency of our findings across heterogeneous contexts highlights graph-theory as a potential gold-standard approach for brain network analysis in bvFTD. Hum Brain Mapp 38:3804–3822, 2017. © 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.  |l eng 
536 |a Detalles de la financiación: 510106, NHMRC, National Health and Medical Research Council 
536 |a Detalles de la financiación: APP1103258, NHMRC, National Health and Medical Research Council 
536 |a Detalles de la financiación: CE11000102, CCD, Centre of Excellence in Cognition and its Disorders, Australian Research Council 
593 |a Institute of Cognitive and Translational Neuroscience (INCyT), INECO Foundation, Favaloro University, Buenos Aires, Argentina 
593 |a National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina 
593 |a Neuroscience Research Australia, Sydney, Australia 
593 |a School of Medical Sciences, The University of New South Wales, Sydney, Australia 
593 |a School of Psychology, Central Clinical School & Brain and Mind Centre, University of Sydney; Neuroscience Research Australia; ARC Centre of Excellence in Cognition and its Disorders, New South Wales, Australia 
593 |a Universidad de los Andes, Bogota, Colombia 
593 |a Intellectus Memory and Cognition Center, Mental Health and Psychiatry Department, Hospital Universitario San Ignacio, Pontificia Universidad Javeriana, Colombia 
593 |a FMRIB, Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, United Kingdom 
593 |a Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, Australia 
593 |a Australian Research Council Centre of Excellence in Cognition and its Disorders, Sydney, Australia 
593 |a Fundación Escuela de Medicina Nuclear (FUESMEN) and Comisión Nacional de Energía Atómica (CNEA), Buenos Aires, Argentina 
593 |a Instituto Balseiro and Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo (UNCuyo), Mendoza, Argentina 
593 |a INECO Neurociencias Oroño, Grupo Oroño, Rosario, Argentina 
593 |a Centro Algoritmi, University of Minho, Guimarães, Portugal 
593 |a Laboratory of Neuroimaging and Neuroscience (LANEN), INECO Foundation Rosario, Rosario, Argentina 
593 |a Physiopathology Department, ICBM Neuroscience Department, Faculty of Medicine, University of Chile, Santiago, Chile 
593 |a Cognitive Neurology and Dementia, Neurology Department, Hospital del Salvador, Providencia, Santiago, Chile 
593 |a Gerosciences Center for Brain Health and Metabolism, Santiago, Chile 
593 |a Centre for Advanced Research in Education, Santiago, Chile 
593 |a Center for Complex Systems & Brain Sciences - Escuela de Ciencia y Tecnologia. UNSAM/Campus Miguelete, Argentina 
593 |a Faculty of Education, National University of Cuyo (UNCuyo), Mendoza, Argentina 
593 |a Universidad Autonoma del Caribe, Barranquilla, Colombia 
593 |a Center for Social and Cognitive Neuroscience (CSCN), School of Psychology, Universidad Adolfo Ibañez, Santiago, Chile 
690 1 0 |a BIOMARKERS 
690 1 0 |a FRONTOTEMPORAL DEMENTIA 
690 1 0 |a FUNCTIONAL CONNECTIVITY 
690 1 0 |a GRAPH-THEORY AND NEURODEGENERATIVE DISEASES 
690 1 0 |a ADULT 
690 1 0 |a ARTICLE 
690 1 0 |a BRAIN MAPPING 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DIAGNOSTIC TEST ACCURACY STUDY 
690 1 0 |a DISEASE CONTROL 
690 1 0 |a FEMALE 
690 1 0 |a FRONTAL VARIANT FRONTOTEMPORAL DEMENTIA 
690 1 0 |a FUNCTIONAL CONNECTIVITY 
690 1 0 |a FUNCTIONAL MAGNETIC RESONANCE IMAGING 
690 1 0 |a GOLD STANDARD 
690 1 0 |a HUMAN 
690 1 0 |a MAJOR CLINICAL STUDY 
690 1 0 |a MALE 
690 1 0 |a MIDDLE AGED 
690 1 0 |a MULTICENTER STUDY 
690 1 0 |a NEUROIMAGING 
690 1 0 |a NUCLEAR MAGNETIC RESONANCE SCANNER 
690 1 0 |a POSTERIOR CINGULATE 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a RESTING STATE NETWORK 
690 1 0 |a SENSITIVITY AND SPECIFICITY 
690 1 0 |a SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY 
690 1 0 |a VOXEL BASED MORPHOMETRY 
653 0 0 |a MRI scanner, Philips MRI Equipment 
700 1 |a Piguet, O. 
700 1 |a Abrevaya, S. 
700 1 |a Desmaras, H. 
700 1 |a García-Cordero, I. 
700 1 |a Baez, S. 
700 1 |a Alethia de la Fuente, L. 
700 1 |a Reyes, P. 
700 1 |a Tu, S. 
700 1 |a Moguilner, S. 
700 1 |a Lori, N. 
700 1 |a Landin-Romero, R. 
700 1 |a Matallana, D. 
700 1 |a Slachevsky, A. 
700 1 |a Torralva, T. 
700 1 |a Chialvo, D. 
700 1 |a Kumfor, F. 
700 1 |a García, A.M. 
700 1 |a Manes, F. 
700 1 |a Hodges, J.R. 
700 1 |a Ibanez, A. 
773 0 |d John Wiley and Sons Inc., 2017  |g v. 38  |h pp. 3804-3822  |k n. 8  |x 10659471  |t Hum. Brain Mapp. 
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