Stroke and Neurodegeneration Induce Different Connectivity Aberrations in the Insula

Background and Purpose - Stroke and neurodegeneration cause significant brain damage and cognitive impairment, especially if the insular cortex is compromised. This study explores for the first time whether these 2 causes differentially alter connectivity patterns in the insular cortex. Methods - Re...

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Autor principal: García-Cordero, I.
Otros Autores: Sedeño, L., Fraiman, D., Craiem, D., De La Fuente, L.A, Salamone, P., Serrano, C., Sposato, L., Manes, F., Ibañez, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Lippincott Williams and Wilkins 2015
Acceso en línea:Registro en Scopus
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100 1 |a García-Cordero, I. 
245 1 0 |a Stroke and Neurodegeneration Induce Different Connectivity Aberrations in the Insula 
260 |b Lippincott Williams and Wilkins  |c 2015 
270 1 0 |m Ibañez, A.; Laboratory of Experimental Psychology and Neuroscience (LPEN), Institute of Cognitive Neurology (INECO), Favaloro University, Pacheco de Melo 1860, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Van Den Heuvel, M.P., Sporns, O., Network hubs in the human brain (2013) Trends Cogn Sci., 17, pp. 683-696 
504 |a Craig, A.D., How do you feel-now? the anterior insula and human awareness (2009) Nat Rev Neurosci., 10, pp. 59-70 
504 |a Ibañez, A., Gleichgerrcht, E., Manes, F., Clinical effects of insular damage in humans (2010) Brain Struct Funct., 214, pp. 397-410 
504 |a Seeley, W.W., Crawford, R.K., Zhou, J., Miller, B.L., Greicius, M.D., Neurodegenerative diseases target large-scale human brain networks (2009) Neuron., 62, pp. 42-52 
504 |a Rascovsky, K., Hodges, J.R., Knopman, D., Mendez, M.F., Kramer, J.H., Neuhaus, J., Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia (2011) Brain., 134, pp. 2456-2477 
504 |a Baez, S., Couto, B., Torralva, T., Sposato, L.A., Huepe, D., Montañes, P., Comparing moral judgments of patients with frontotemporal dementia and frontal stroke (2014) JAMA Neurol., 71, pp. 1172-1176 
504 |a Grefkes, C., Fink, G.R., Connectivity-based approaches in stroke and recovery of function (2014) Lancet Neurol., 13, pp. 206-216 
504 |a Pievani, M., Filippini, N., Van Den Heuvel, M.P., Cappa, S.F., Frisoni, G.B., Brain connectivity in neurodegenerative diseases-from phenotype to proteinopathy (2014) Nat Rev Neurol., 10, pp. 620-633 
504 |a Day, G.S., Farb, N.A., Tang-Wai, D.F., Masellis, M., Black, S.E., Freedman, M., Salience network resting-state activity: Prediction of frontotemporal dementia progression (2013) JAMA Neurol., 70, pp. 1249-1253 
504 |a Pasquini, L., Scherr, M., Tahmasian, M., Meng, C., Myers, N.E., Ortner, M., Link between hippocampus' raised local and eased global intrinsic connectivity in AD (2015) Alzheimers Dement., 11, pp. 475-484 
504 |a Zang, Y., Jiang, T., Lu, Y., He, Y., Tian, L., Regional homogeneity approach to fMRI data analysis (2004) Neuroimage., 22, pp. 394-400 
504 |a Simmons, W.K., Avery, J.A., Barcalow, J.C., Bodurka, J., Drevets, W.C., Bellgowan, P., Keeping the body in mind: Insula functional organization and functional connectivity integrate interoceptive, exteroceptive, and emotional awareness (2013) Hum Brain Mapp., 34, pp. 2944-2958 
504 |a Carmichael, S.T., Plasticity of cortical projections after stroke (2003) Neuroscientist., 9, pp. 64-75 
504 |a Ibañez, A., Manes, F., Contextual social cognition and the behavioral variant of frontotemporal dementia (2012) Neurology., 78, pp. 1354-1362 
504 |a Crossley, N.A., Mechelli, A., Scott, J., Carletti, F., Fox, P.T., McGuire, P., The hubs of the human connectome are generally implicated in the anatomy of brain disorders (2014) Brain., 137, pp. 2382-2395 
520 3 |a Background and Purpose - Stroke and neurodegeneration cause significant brain damage and cognitive impairment, especially if the insular cortex is compromised. This study explores for the first time whether these 2 causes differentially alter connectivity patterns in the insular cortex. Methods - Resting state-functional magnetic resonance imaging data were collected from patients with insular stroke, patients with behavioral variant frontotemporal dementia, and healthy controls. Data from the 3 groups were assessed through a correlation function analysis. Specifically, we compared decreases in connectivity as a function of voxel Euclidean distance within the insular cortex. Results - Relative to controls, patients with stroke showed faster connectivity decays as a function of distance (hypoconnectivity). In contrast, the behavioral variant frontotemporal dementia group exhibited significant hyperconnectivity between neighboring voxels. Both patient groups evinced global hypoconnectivity. No between-group differences were observed in a volumetrically and functionally comparable region without ischemia or neurodegeneration. Conclusions - Functional insular cortex connectivity is affected differently by cerebral ischemia and neurodegeneration, possibly because of differences in the cause-specific pathophysiological mechanisms of each disease. These findings have important clinical and theoretical implications. © 2015 American Heart Association, Inc.  |l eng 
593 |a Laboratory of Experimental Psychology and Neuroscience (LPEN), Institute of Cognitive Neurology (INECO), Favaloro University, Pacheco de Melo 1860, Buenos Aires, Argentina 
593 |a UDP-INECO Foundation Core on Neuroscience (UIFCoN), Faculty of Psychology, Diego Portales University, Santiago, Chile 
593 |a National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina 
593 |a Laboratorio de Investigación en Neurociencia, Universidad de San Andrés, Buenos Aires, Argentina 
593 |a Facultad de Ingeniería, Ciencias Exactas y Naturales, Universidad Favaloro, Buenos Aires, Argentina 
593 |a Memory and Balance Clinic, Buenos Aires, Argentina 
593 |a Department of Clinical Neurological Sciences, Western University, London, Canada 
593 |a Universidad Autónoma Del Caribe, Barranquilla, Colombia 
593 |a ACR Centre of Excellence in Cognition and Its Disorders, Sydney, Australia 
690 1 0 |a CEREBRAL CORTEX 
690 1 0 |a DEMENTIA 
690 1 0 |a MAGNETIC RESONANCE IMAGING 
690 1 0 |a STROKE 
690 1 0 |a ADULT 
690 1 0 |a AGED 
690 1 0 |a ARTICLE 
690 1 0 |a CEREBROSPINAL FLUID 
690 1 0 |a CEREBROVASCULAR ACCIDENT 
690 1 0 |a CLINICAL ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CUNEUS 
690 1 0 |a FEMALE 
690 1 0 |a FRONTAL VARIANT FRONTOTEMPORAL DEMENTIA 
690 1 0 |a FUNCTIONAL MAGNETIC RESONANCE IMAGING 
690 1 0 |a GRAY MATTER 
690 1 0 |a HUMAN 
690 1 0 |a INSULA 
690 1 0 |a INTELLIGENCE QUOTIENT 
690 1 0 |a MALE 
690 1 0 |a NERVE CELL NETWORK 
690 1 0 |a NERVE DEGENERATION 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a SALIENCE NETWORK 
690 1 0 |a STROKE PATIENT 
690 1 0 |a VOXEL BASED MORPHOMETRY 
690 1 0 |a WHITE MATTER 
690 1 0 |a BRAIN CORTEX 
690 1 0 |a BRAIN ISCHEMIA 
690 1 0 |a CEREBROVASCULAR ACCIDENT 
690 1 0 |a CONNECTOME 
690 1 0 |a FRONTOTEMPORAL DEMENTIA 
690 1 0 |a MIDDLE AGED 
690 1 0 |a NUCLEAR MAGNETIC RESONANCE IMAGING 
690 1 0 |a PATHOPHYSIOLOGY 
690 1 0 |a AGED 
690 1 0 |a BRAIN ISCHEMIA 
690 1 0 |a CEREBRAL CORTEX 
690 1 0 |a CONNECTOME 
690 1 0 |a FEMALE 
690 1 0 |a FRONTOTEMPORAL DEMENTIA 
690 1 0 |a HUMANS 
690 1 0 |a MAGNETIC RESONANCE IMAGING 
690 1 0 |a MALE 
690 1 0 |a MIDDLE AGED 
690 1 0 |a STROKE 
700 1 |a Sedeño, L. 
700 1 |a Fraiman, D. 
700 1 |a Craiem, D. 
700 1 |a De La Fuente, L.A. 
700 1 |a Salamone, P. 
700 1 |a Serrano, C. 
700 1 |a Sposato, L. 
700 1 |a Manes, F. 
700 1 |a Ibañez, A. 
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