Damage to the cingulum contributes to alzheimer's disease pathophysiology by deafferentation mechanism

This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty‐one patients with probable AD, 23 with amnestic mild cognitive impairment (a‐MCI), and 14 health...

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Published inHuman brain mapping Vol. 33; no. 6; pp. 1295 - 1308
Main Authors Bozzali, Marco, Giulietti, Giovanni, Basile, Barbara, Serra, Laura, Spanò, Barbara, Perri, Roberta, Giubilei, Franco, Marra, Camillo, Caltagirone, Carlo, Cercignani, Mara
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.06.2012
Wiley-Liss
John Wiley & Sons, Inc
Subjects
Online AccessGet full text
ISSN1065-9471
1097-0193
1097-0193
DOI10.1002/hbm.21287

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Abstract This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty‐one patients with probable AD, 23 with amnestic mild cognitive impairment (a‐MCI), and 14 healthy subjects underwent MRI scanning at 3T. Voxel‐based morphometry was used to assess regional GM atrophy in AD and a‐MCI patients. Diffusion tensor‐MRI tractography was used to reconstruct the cingulum bilaterally, and to quantify, voxel‐by‐voxel, its fractional anisotropy (FA) and mean diffusivity (MD) (measures of microscopic WM integrity). Atrophy of the cinguli was also assessed by means of jacobian determinants (JD) of local transformations. In AD patients, four clusters of reduced GM were found nearby the cinguli, in the posterior (PCC) and anterior cingulate cortex, and in the hippocampal/parahippocampal areas. Widespread areas of reduced FA and increased MD were found in the cinguli of both, AD and a‐MCI patients. A region of macroscopic atrophy was detectable in AD patients only. Strong associations were found between local GM densities in the four identified clusters, and measures of micro‐ and (to a lesser extent) macroscopic damage of patients' cinguli. Linear regression analyses revealed that MD in the cinguli predicts patients' measures of episodic memory in combination with GM density of hippocampal/parahippocampal areas, and measures of global cognition in combination with GM density of the PCC. This study indicates that brain deafferentation though the cingulum is likely to play a remarkable role in progressive development of cognitive impairment in AD. Hum Brain Mapp, 2011. © 2011 Wiley‐Liss, Inc.
AbstractList This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty‐one patients with probable AD, 23 with amnestic mild cognitive impairment (a‐MCI), and 14 healthy subjects underwent MRI scanning at 3T. Voxel‐based morphometry was used to assess regional GM atrophy in AD and a‐MCI patients. Diffusion tensor‐MRI tractography was used to reconstruct the cingulum bilaterally, and to quantify, voxel‐by‐voxel, its fractional anisotropy (FA) and mean diffusivity (MD) (measures of microscopic WM integrity). Atrophy of the cinguli was also assessed by means of jacobian determinants (JD) of local transformations. In AD patients, four clusters of reduced GM were found nearby the cinguli, in the posterior (PCC) and anterior cingulate cortex, and in the hippocampal/parahippocampal areas. Widespread areas of reduced FA and increased MD were found in the cinguli of both, AD and a‐MCI patients. A region of macroscopic atrophy was detectable in AD patients only. Strong associations were found between local GM densities in the four identified clusters, and measures of micro‐ and (to a lesser extent) macroscopic damage of patients' cinguli. Linear regression analyses revealed that MD in the cinguli predicts patients' measures of episodic memory in combination with GM density of hippocampal/parahippocampal areas, and measures of global cognition in combination with GM density of the PCC. This study indicates that brain deafferentation though the cingulum is likely to play a remarkable role in progressive development of cognitive impairment in AD. Hum Brain Mapp, 2011. © 2011 Wiley‐Liss, Inc.
This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty-one patients with probable AD, 23 with amnestic mild cognitive impairment (a-MCI), and 14 healthy subjects underwent MRI scanning at 3T. Voxel-based morphometry was used to assess regional GM atrophy in AD and a-MCI patients. Diffusion tensor-MRI tractography was used to reconstruct the cingulum bilaterally, and to quantify, voxel-by-voxel, its fractional anisotropy (FA) and mean diffusivity (MD) (measures of microscopic WM integrity). Atrophy of the cinguli was also assessed by means of jacobian determinants (JD) of local transformations. In AD patients, four clusters of reduced GM were found nearby the cinguli, in the posterior (PCC) and anterior cingulate cortex, and in the hippocampal/parahippocampal areas. Widespread areas of reduced FA and increased MD were found in the cinguli of both, AD and a-MCI patients. A region of macroscopic atrophy was detectable in AD patients only. Strong associations were found between local GM densities in the four identified clusters, and measures of micro- and (to a lesser extent) macroscopic damage of patients' cinguli. Linear regression analyses revealed that MD in the cinguli predicts patients' measures of episodic memory in combination with GM density of hippocampal/parahippocampal areas, and measures of global cognition in combination with GM density of the PCC. This study indicates that brain deafferentation though the cingulum is likely to play a remarkable role in progressive development of cognitive impairment in AD.
This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty-one patients with probable AD, 23 with amnestic mild cognitive impairment (a-MCI), and 14 healthy subjects underwent MRI scanning at 3T. Voxel-based morphometry was used to assess regional GM atrophy in AD and a-MCI patients. Diffusion tensor-MRI tractography was used to reconstruct the cingulum bilaterally, and to quantify, voxel-by-voxel, its fractional anisotropy (FA) and mean diffusivity (MD) (measures of microscopic WM integrity). Atrophy of the cinguli was also assessed by means of jacobian determinants (JD) of local transformations. In AD patients, four clusters of reduced GM were found nearby the cinguli, in the posterior (PCC) and anterior cingulate cortex, and in the hippocampal/parahippocampal areas. Widespread areas of reduced FA and increased MD were found in the cinguli of both, AD and a-MCI patients. A region of macroscopic atrophy was detectable in AD patients only. Strong associations were found between local GM densities in the four identified clusters, and measures of micro- and (to a lesser extent) macroscopic damage of patients' cinguli. Linear regression analyses revealed that MD in the cinguli predicts patients' measures of episodic memory in combination with GM density of hippocampal/parahippocampal areas, and measures of global cognition in combination with GM density of the PCC. This study indicates that brain deafferentation though the cingulum is likely to play a remarkable role in progressive development of cognitive impairment in AD.This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty-one patients with probable AD, 23 with amnestic mild cognitive impairment (a-MCI), and 14 healthy subjects underwent MRI scanning at 3T. Voxel-based morphometry was used to assess regional GM atrophy in AD and a-MCI patients. Diffusion tensor-MRI tractography was used to reconstruct the cingulum bilaterally, and to quantify, voxel-by-voxel, its fractional anisotropy (FA) and mean diffusivity (MD) (measures of microscopic WM integrity). Atrophy of the cinguli was also assessed by means of jacobian determinants (JD) of local transformations. In AD patients, four clusters of reduced GM were found nearby the cinguli, in the posterior (PCC) and anterior cingulate cortex, and in the hippocampal/parahippocampal areas. Widespread areas of reduced FA and increased MD were found in the cinguli of both, AD and a-MCI patients. A region of macroscopic atrophy was detectable in AD patients only. Strong associations were found between local GM densities in the four identified clusters, and measures of micro- and (to a lesser extent) macroscopic damage of patients' cinguli. Linear regression analyses revealed that MD in the cinguli predicts patients' measures of episodic memory in combination with GM density of hippocampal/parahippocampal areas, and measures of global cognition in combination with GM density of the PCC. This study indicates that brain deafferentation though the cingulum is likely to play a remarkable role in progressive development of cognitive impairment in AD.
This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical progression of Alzheimer's disease (AD). Thirty-one patients with probable AD, 23 with amnestic mild cognitive impairment (a-MCI), and 14 healthy subjects underwent MRI scanning at 3T. Voxel-based morphometry was used to assess regional GM atrophy in AD and a-MCI patients. Diffusion tensor-MRI tractography was used to reconstruct the cingulum bilaterally, and to quantify, voxel-by-voxel, its fractional anisotropy (FA) and mean diffusivity (MD) (measures of microscopic WM integrity). Atrophy of the cinguli was also assessed by means of jacobian determinants (JD) of local transformations. In AD patients, four clusters of reduced GM were found nearby the cinguli, in the posterior (PCC) and anterior cingulate cortex, and in the hippocampal/parahippocampal areas. Widespread areas of reduced FA and increased MD were found in the cinguli of both, AD and a-MCI patients. A region of macroscopic atrophy was detectable in AD patients only. Strong associations were found between local GM densities in the four identified clusters, and measures of micro- and (to a lesser extent) macroscopic damage of patients' cinguli. Linear regression analyses revealed that MD in the cinguli predicts patients' measures of episodic memory in combination with GM density of hippocampal/parahippocampal areas, and measures of global cognition in combination with GM density of the PCC. This study indicates that brain deafferentation though the cingulum is likely to play a remarkable role in progressive development of cognitive impairment in AD. Hum Brain Mapp, 2011. © 2011 Wiley-Liss, Inc. [PUBLICATION ABSTRACT]
Author Cercignani, Mara
Serra, Laura
Giubilei, Franco
Marra, Camillo
Basile, Barbara
Caltagirone, Carlo
Giulietti, Giovanni
Spanò, Barbara
Perri, Roberta
Bozzali, Marco
AuthorAffiliation 3 Department of Clinical and Behavioural Neurology, Santa Lucia Foundation, IRCCS, Via Ardeatina 306, 00179 Rome, Italy
5 Institute of Neurology, Università Cattolica, L.go A. Gemelli 8, 00168 Rome, Italy
2 Laboratorio di Neurobioimmagini, IRCCS Centro Neurolesi ‘Bonino‐Pulejo’, S.S. 113, Via Palermo, Cntr. Casazza, 98124 Messina, Italy
6 Department of Neuroscience, University of Rome ‘Tor Vergata’, Via Mont Pelier 1, 00133 Rome, Italy
4 Department of Neurological Science, II Faculty of Medicine, ‘Sapienza’ University of Rome, Via di Grottarossa 1035, I‐00189, Rome, Italy
1 Neuroimaging Laboratory, Santa Lucia Foundation, IRCCS, Via Ardeatina 306, 00179 Rome, Italy
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ContentType Journal Article
Copyright Copyright © 2011 Wiley‐Liss, Inc.
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Issue 6
Keywords VBM
Nervous system diseases
AD
Pathophysiology
Radiodiagnosis
Alzheimer disease
Tractography
Nuclear magnetic resonance imaging
Cerebral disorder
MCI
cingulum
Central nervous system disease
DT-MRI
Degenerative disease
Deafferentation
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
Copyright © 2011 Wiley-Liss, Inc.
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PublicationTitle Human brain mapping
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PublicationYear 2012
Publisher Wiley Subscription Services, Inc., A Wiley Company
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References Heiervang E, Behrens TE, Mackay CE, Robson MD, Johansen-Berg H ( 2006): Between session reproducibility and between subject variability of diffusion MR and tractography measures. Neuroimage 33: 867-877.
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Parker GJ, Haroon HA, Wheeler-Kingshott CA ( 2003): A framework for a streamline-based probabilistic index of connectivity (PICo) using a structural interpretation of MRI diffusion measurements. J Magn Reson Imaging 18: 242-254.
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Worsley KJ, Evans AC, Marrett S, Neelin P ( 1992): A three-dimensional statistical analysis for CBF activation studies in human brain. J Cereb Blood Flow Metab 12: 900-918.
Bozzali M, Falini A, Franceschi M, Cercignani M, Zuffi M, Scotti G, Comi G, Filippi M ( 2002): White matter damage in Alzheimer's disease assessed in vivo using diffusion tensor magnetic resonance imaging. J Neurol Neurosurg Psychiatry 72: 742-746.
Whitwell JL, Przybelski SA, Weigand SD, Knopman DS, Boeve BF, Petersen RC, Jack CR Jr ( 2007): 3D maps from multiple MRI illustrate changing atrophy patterns as subjects progress from mild cognitive impairment to Alzheimer's disease. Brain 130: 1777-1786.
Chételat G, Landeau B, Eustache F, Mézenge F, Viader F, de la Sayette V, Desgranges B, Baron JC ( 2005): Using voxel-based morphometry to map the structural changes associated with rapid conversion in MCI: a longitudinal MRI study. Neuroimage 27: 934-946.
Ashburner J, Friston KJ ( 2005): Unified segmentation. Neuroimage 26: 839-851.
Magni E, Binetti G, Padovani A, Cappa SF, Bianchetti A, Trabucchi M ( 1996): The Mini-Mental State Examination in Alzheimer's disease and multi-infarct dementia. Int Psychogeriatr 8: 127-134.
Bozzali M, Filippi M, Magnani G, Cercignani M, Franceschi M, Schiatti E, Castiglioni S, Mossini R, Falautano M, Scotti G, Comi G, Falini A ( 2006): The contribution of voxel-based morphometry in staging patients with mild cognitive impairment. Neurology 67: 453-460.
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Pierpaoli C, Basser PJ ( 1996): Toward a quantitative assessment of diffusion anisotropy. Magn Reson Med 36: 893-906.
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Braak H, Braak E ( 1991): Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 82: 239-259.
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Pajevic S, Pierpaoli C ( 1999): Color schemes to represent the orientation of anisotropic tissues from diffusion tensor data: Application to white matter fiber tract mapping in the human brain. Magn Reson Med 42: 526-540.
Chételat G, Villemagne VL, Bourgeat P, Pike KE, Jones G, Ames D, Ellis KA, Szoeke C, Martins RN, O'Keefe GJ, Salvado O, Masters CL, Rowe CC ( 2010): Relationship between atrophy and beta-amyloid deposition in Alzheimer disease. Ann Neurol 67: 317-324.
Villain N, Fouquet M, Baron JC, Mézenge F, Landeau B, de La Sayette V, Viader F, Eustache F, Desgranges B, Chételat G ( 2010): Sequential relationships between grey matter and white matter atrophy and brain metabolic abnormalities in early Alzheimer's disease. Brain 133: 3301-3314.
Ashburner J, Friston KJ ( 2000): Voxel-based morphometry-the methods. Neuroimage 11: 805-821.
Buckner RL ( 2004): Memory and executive function in aging and AD: multiple factors that cause decline and reserve factors that compensate. Neuron 44: 195-208.
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM ( 1984): Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 34: 939-944.
Catheline G, Periot O, Amirault M, Braun M, Dartigues JF, Auriacombe S, Allard M ( 2010): Distinctive alterations of the cingulum bundle during aging and Alzheimer's disease. Neurobiol Aging 31: 1582-1592.
Braak H, Braak E ( 1995): Staging of Alzheimer's disease-related neurofibrillary changes. Neurobiol Aging 16: 271-278; discussion 278-284.
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Gili T, Cercignani M, Serra L, Perri R, Giove F, Maraviglia B, Caltagirone C, Bozzali M ( 2011): Regional brain atrophy and functional disconnection across Alzheimer's disease evolution. J Neurol Neurosurg Psychiatry 82: 58-66.
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Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC, Rabins PV, Ritchie K, Rossor M, Thal L, Winblad B ( 2001): Current concepts in mild cognitive impairment. Arch Neurol 58: 1985-1992.
Serra L, Perri R, Cercignani M, Spanò B, Fadda L, Marra C, Carlesimo GA, Caltagirone C, Bozzali M ( 2010b): Are the Behavioral Symptoms of Alzheimer's Disease Directly Associated with Neurodegeneration? J Alzheimers Dis 21: 627-639.
Xie S, Xiao JX, Wang YH, Wu HK, Gong GL, Jiang XX ( 2005): Evaluation of bilateral cingulum with tractography in patients with Alzheimer's disease. Neuroreport 16: 1275-1278.
Villain N, Desgranges B, Viader F, de la Sayette V, Mézenge F, Landeau B, Baron JC, Eustache F, Chételat G ( 2008): Relationships between hippocampal atrophy, white matter disruption, and gray matter hypometabolism in Alzheimer's disease. J Neurosci 28: 6174-6181.
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Greicius MD, Srivastava
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References_xml – reference: Greicius MD, Krasnow B, Reiss AL, Menon V ( 2003): Functional connectivity in the resting brain: a network analysis of the default mode hypothesis. Proc Natl Acad Sci U S A 100: 253-258.
– reference: Sorg C, Riedl V, Mühlau M, Calhoun VD, Eichele T, Läer L, Drzezga A, Förstl H, Kurz A, Zimmer C, Wohlschläger AM ( 2007): Selective changes of resting-state networks in individuals at risk for Alzheimer's disease. Proc Natl Acad Sci U S A 104: 18760-18765.
– reference: De Blese R, Denes G, Luzzatti C, Mazzocchi A, Poeck K, Spinnler H, Willmes K ( 1986): L'Aachener Aphasie test I: Problemi e soluzioni per una versione italiana del test e per uno studio crosslinguistico dei disturbi afasici. Arch Psicol Neurol Psichiatr 47: 209-236.
– reference: Ashburner J, Friston KJ ( 2005): Unified segmentation. Neuroimage 26: 839-851.
– reference: Bozzali M, Filippi M, Magnani G, Cercignani M, Franceschi M, Schiatti E, Castiglioni S, Mossini R, Falautano M, Scotti G, Comi G, Falini A ( 2006): The contribution of voxel-based morphometry in staging patients with mild cognitive impairment. Neurology 67: 453-460.
– reference: Choo IH, Lee DY, Oh JS, Lee JS, Lee DS, Song IC, et al. ( 2010): Posterior cingulate cortex atrophy and regional cingulum disruption in mild cognitive impairment and Alzheimer's disease. Neurobiol Aging 31: 772-779.
– reference: Mosconi L ( 2005): Brain glucose metabolism in the early and specific diagnosis of Alzheimer's disease. FDG-PET studies in MCI and AD. Eur J Nucl Med Mol Imaging 32: 486-510.
– reference: Braak H, Braak E ( 1991): Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol 82: 239-259.
– reference: Pengas G, Hodges JR, Watson P, Nestor PJ ( 2010): Focal posterior cingulate atrophy in incipient Alzheimer's disease. Neurobiol Aging 31 25-33.
– reference: Pajevic S, Pierpaoli C ( 1999): Color schemes to represent the orientation of anisotropic tissues from diffusion tensor data: Application to white matter fiber tract mapping in the human brain. Magn Reson Med 42: 526-540.
– reference: Fellgiebel A, Müller MJ, Wille P, Dellani PR, Scheurich A, Schmidt LG, et al. ( 2005): Color-coded diffusion-tensor-imaging of posterior cingulate fiber tracts in mild cognitive impairment. Neurobiol Aging 26: 1193-1198.
– reference: Bozzali M, Falini A, Franceschi M, Cercignani M, Zuffi M, Scotti G, Comi G, Filippi M ( 2002): White matter damage in Alzheimer's disease assessed in vivo using diffusion tensor magnetic resonance imaging. J Neurol Neurosurg Psychiatry 72: 742-746.
– reference: Raichle ME, Snyder AZ ( 2007): A default mode of brain function: A brief history of an evolving idea. Neuroimage 37: 1083-1090; discussion 1097-1099.
– reference: Parker GJ, Haroon HA, Wheeler-Kingshott CA ( 2003): A framework for a streamline-based probabilistic index of connectivity (PICo) using a structural interpretation of MRI diffusion measurements. J Magn Reson Imaging 18: 242-254.
– reference: Serra L, Cercignani M, Lenzi D, Perri R, Fadda L, Caltagirone C, Macaluso E, Bozzali M ( 2010a): Grey and white matter changes at different stages of Alzheimer's disease. J Alzheimers Dis 19: 47-59.
– reference: Pierpaoli C, Basser PJ ( 1996): Toward a quantitative assessment of diffusion anisotropy. Magn Reson Med 36: 893-906.
– reference: Heiervang E, Behrens TE, Mackay CE, Robson MD, Johansen-Berg H ( 2006): Between session reproducibility and between subject variability of diffusion MR and tractography measures. Neuroimage 33: 867-877.
– reference: Nocentini U, Di Vincenzo S, Panella M, Pasqualetti P, Caltagirone C ( 2002). La valutazione delle funzioni esecutive nella pratica neuropsicologica: dal Modified Card Sorting Test al Modified Card Sorting Test-Roma Version. Dati di standardizzazione. Nuova Rivista di Neurologia 12: 14-24.
– reference: Bozzali M, Franceschi M, Falini A, Pontesilli S, Cercignani M, Magnani G, Scotti G, Comi G, Filippi M ( 2001): Quantification of tissue damage in AD using diffusion tensor and magnetization transfer MRI. Neurology 57: 1135-1137.
– reference: Gili T, Cercignani M, Serra L, Perri R, Giove F, Maraviglia B, Caltagirone C, Bozzali M ( 2011): Regional brain atrophy and functional disconnection across Alzheimer's disease evolution. J Neurol Neurosurg Psychiatry 82: 58-66.
– reference: McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM ( 1984): Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 34: 939-944.
– reference: Good CD, Johnsrude IS, Ashburner J, Henson RN, Friston KJ, Frackowiak RS ( 2001): A voxel-based morphometric study of ageing in 465 normal adult human brains. Neuroimage 14: 21-36.
– reference: Scahill RI, Schott JM, Stevens JM, Rossor MN, Fox NC ( 2002): Mapping the evolution of regional atrophy in Alzheimer's disease: Unbiased analysis of fluid-registered serial MRI. Proc Natl Acad Sci USA 99: 4703-4707.
– reference: Worsley KJ, Evans AC, Marrett S, Neelin P ( 1992): A three-dimensional statistical analysis for CBF activation studies in human brain. J Cereb Blood Flow Metab 12: 900-918.
– reference: Buckner RL ( 2004): Memory and executive function in aging and AD: multiple factors that cause decline and reserve factors that compensate. Neuron 44: 195-208.
– reference: Orsini A, Grossi D, Capitani E, Laiacona M, Papagno C, Vallar G ( 1987): Verbal and spatial immediate memory span: Normative data from 1355 adults and 1112 children. Ital J Neurol Sci 8: 539-554.
– reference: Serra L, Perri R, Cercignani M, Spanò B, Fadda L, Marra C, Carlesimo GA, Caltagirone C, Bozzali M ( 2010b): Are the Behavioral Symptoms of Alzheimer's Disease Directly Associated with Neurodegeneration? J Alzheimers Dis 21: 627-639.
– reference: Braak H, Braak E ( 1995): Staging of Alzheimer's disease-related neurofibrillary changes. Neurobiol Aging 16: 271-278; discussion 278-284.
– reference: Chételat G, Landeau B, Eustache F, Mézenge F, Viader F, de la Sayette V, Desgranges B, Baron JC ( 2005): Using voxel-based morphometry to map the structural changes associated with rapid conversion in MCI: a longitudinal MRI study. Neuroimage 27: 934-946.
– reference: Magni E, Binetti G, Padovani A, Cappa SF, Bianchetti A, Trabucchi M ( 1996): The Mini-Mental State Examination in Alzheimer's disease and multi-infarct dementia. Int Psychogeriatr 8: 127-134.
– reference: Chételat G, Villemagne VL, Bourgeat P, Pike KE, Jones G, Ames D, Ellis KA, Szoeke C, Martins RN, O'Keefe GJ, Salvado O, Masters CL, Rowe CC ( 2010): Relationship between atrophy and beta-amyloid deposition in Alzheimer disease. Ann Neurol 67: 317-324.
– reference: Jenkinson M, Smith S ( 2001): A global optimisation method for robust affine registration of brain images. Med Image Anal 5: 143-156.
– reference: Greicius MD, Srivastava G, Reiss AL, Menon V ( 2004): Default-mode network activity distinguishes Alzheimer's disease from healthy aging: evidence from functional MRI. Proc Natl Acad Sci U S A 101: 4637-4642.
– reference: Whitwell JL, Przybelski SA, Weigand SD, Knopman DS, Boeve BF, Petersen RC, Jack CR Jr ( 2007): 3D maps from multiple MRI illustrate changing atrophy patterns as subjects progress from mild cognitive impairment to Alzheimer's disease. Brain 130: 1777-1786.
– reference: Xie S, Xiao JX, Wang YH, Wu HK, Gong GL, Jiang XX ( 2005): Evaluation of bilateral cingulum with tractography in patients with Alzheimer's disease. Neuroreport 16: 1275-1278.
– reference: Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC, Rabins PV, Ritchie K, Rossor M, Thal L, Winblad B ( 2001): Current concepts in mild cognitive impairment. Arch Neurol 58: 1985-1992.
– reference: Petersen RC ( 2004): Mild cognitive impairment as a diagnostic entity. J Intern Med 256: 183-194.
– reference: Alexander DC, Pierpaoli C, Basser PJ, Gee JC ( 2001): Spatial transformations of diffusion tensor magnetic resonance images. IEEE Trans Med Imaging 20: 1131-1139.
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SSID ssj0011501
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Snippet This study investigates the differential contribution of gray matter (GM) atrophy and deafferentation through white matter (WM) damage in the clinical...
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StartPage 1295
SubjectTerms Aged
Aged, 80 and over
Alzheimer Disease - pathology
Alzheimer Disease - physiopathology
Atrophy - pathology
Atrophy - physiopathology
Biological and medical sciences
cingulum
Cognitive Dysfunction - pathology
Cognitive Dysfunction - physiopathology
deafferentation
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Diffusion Tensor Imaging
Disease Progression
DT-MRI
Female
Gyrus Cinguli - pathology
Gyrus Cinguli - physiopathology
Humans
Investigative techniques, diagnostic techniques (general aspects)
Magnetic Resonance Imaging
Male
MCI
Medical sciences
Middle Aged
Nerve Fibers, Myelinated - pathology
Nerve Fibers, Unmyelinated - pathology
Nervous system
Neurology
Radiodiagnosis. Nmr imagery. Nmr spectrometry
tractography
VBM
Title Damage to the cingulum contributes to alzheimer's disease pathophysiology by deafferentation mechanism
URI https://api.istex.fr/ark:/67375/WNG-8HJCVVC6-9/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.21287
https://www.ncbi.nlm.nih.gov/pubmed/21520352
https://www.proquest.com/docview/1517356791
https://www.proquest.com/docview/1012746375
https://pubmed.ncbi.nlm.nih.gov/PMC6870125
Volume 33
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