The neural basis of visuospatial perception in Alzheimer's disease and healthy elderly comparison subjects: An fMRI study
The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients with Alzheimer's disease compared with healthy elderly comparison subjects using functional magnetic resonance imaging (fMRI). Twelv...
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Published in | Psychiatry research. Neuroimaging Vol. 172; no. 2; pp. 109 - 116 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ireland Ltd
15.05.2009
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Abstract | The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients with Alzheimer's disease compared with healthy elderly comparison subjects using functional magnetic resonance imaging (fMRI). Twelve patients with AD and thirteen elderly comparison subjects were investigated. The patients were recruited from the local clinic and comparison subjects were from spouses and community. All participants underwent fMRI whilst viewing visuospatial stimuli and structural MRI, and findings were analysed using voxel-based morphometry. The comparison group activated V5, superior parietal lobe, parieto-occipital cortex and premotor cortices. The AD group demonstrated hypoactivation in the above regions and instead showed greater activation in inferior parietal lobule and activated additional areas. There was no structural atrophy above and beyond that found globally in patients in the identified regions of BOLD activation. To our knowledge, this is the first study to explore the neuroanatomy of perception of depth and motion in Alzheimer's disease. These specific functional deficits in AD provide evidence for an underlying patho-physiological basis for the clinically important symptom of visuospatial disorientation in patients with AD. |
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AbstractList | Abstract The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients with Alzheimer's disease compared with healthy elderly comparison subjects using functional magnetic resonance imaging (fMRI). Twelve patients with AD and thirteen elderly comparison subjects were investigated. The patients were recruited from the local clinic and comparison subjects were from spouses and community. All participants underwent fMRI whilst viewing visuospatial stimuli and structural MRI, and findings were analysed using voxel-based morphometry. The comparison group activated V5, superior parietal lobe, parieto-occipital cortex and premotor cortices. The AD group demonstrated hypoactivation in the above regions and instead showed greater activation in inferior parietal lobule and activated additional areas. There was no structural atrophy above and beyond that found globally in patients in the identified regions of BOLD activation. To our knowledge, this is the first study to explore the neuroanatomy of perception of depth and motion in Alzheimer's disease. These specific functional deficits in AD provide evidence for an underlying patho-physiological basis for the clinically important symptom of visuospatial disorientation in patients with AD. The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients with Alzheimer's disease compared with healthy elderly comparison subjects using functional magnetic resonance imaging (fMRI). Twelve patients with AD and thirteen elderly comparison subjects were investigated. The patients were recruited from the local clinic and comparison subjects were from spouses and community. All participants underwent fMRI whilst viewing visuospatial stimuli and structural MRI, and findings were analysed using voxel-based morphometry. The comparison group activated V5, superior parietal lobe, parieto-occipital cortex and premotor cortices. The AD group demonstrated hypoactivation in the above regions and instead showed greater activation in inferior parietal lobule and activated additional areas. There was no structural atrophy above and beyond that found globally in patients in the identified regions of BOLD activation. To our knowledge, this is the first study to explore the neuroanatomy of perception of depth and motion in Alzheimer's disease. These specific functional deficits in AD provide evidence for an underlying patho-physiological basis for the clinically important symptom of visuospatial disorientation in patients with AD. The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients with Alzheimer's disease compared with healthy elderly comparison subjects using functional magnetic resonance imaging (fMRI). Twelve patients with AD and thirteen elderly comparison subjects were investigated. The patients were recruited from the local clinic and comparison subjects were from spouses and community. All participants underwent fMRI whilst viewing visuospatial stimuli and structural MRI, and findings were analysed using voxel-based morphometry. The comparison group activated V5, superior parietal lobe, parieto-occipital cortex and premotor cortices. The AD group demonstrated hypoactivation in the above regions and instead showed greater activation in inferior parietal lobule and activated additional areas. There was no structural atrophy above and beyond that found globally in patients in the identified regions of BOLD activation. To our knowledge, this is the first study to explore the neuroanatomy of perception of depth and motion in Alzheimer's disease. These specific functional deficits in AD provide evidence for an underlying patho-physiological basis for the clinically important symptom of visuospatial disorientation in patients with AD.The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients with Alzheimer's disease compared with healthy elderly comparison subjects using functional magnetic resonance imaging (fMRI). Twelve patients with AD and thirteen elderly comparison subjects were investigated. The patients were recruited from the local clinic and comparison subjects were from spouses and community. All participants underwent fMRI whilst viewing visuospatial stimuli and structural MRI, and findings were analysed using voxel-based morphometry. The comparison group activated V5, superior parietal lobe, parieto-occipital cortex and premotor cortices. The AD group demonstrated hypoactivation in the above regions and instead showed greater activation in inferior parietal lobule and activated additional areas. There was no structural atrophy above and beyond that found globally in patients in the identified regions of BOLD activation. To our knowledge, this is the first study to explore the neuroanatomy of perception of depth and motion in Alzheimer's disease. These specific functional deficits in AD provide evidence for an underlying patho-physiological basis for the clinically important symptom of visuospatial disorientation in patients with AD. |
Author | Young, Claire Hunter, Michael D. Thiyagesh, Subha N. Parks, Randolph W. Wilkinson, Iain D. Woodruff, Peter W.R. Farrow, Tom F.D. Accosta-Mesa, Hector |
Author_xml | – sequence: 1 givenname: Subha N. surname: Thiyagesh fullname: Thiyagesh, Subha N. email: s.thiyagesh@sheffield.ac.uk organization: Sheffield Cognition and Neuroimaging Laboratory (SCANLab), Academic Clinical Psychiatry, University of Sheffield, The Longley Centre, Norwood Grange Drive, Sheffield S5 7JT, UK – sequence: 2 givenname: Tom F.D. surname: Farrow fullname: Farrow, Tom F.D. organization: Sheffield Cognition and Neuroimaging Laboratory (SCANLab), Academic Clinical Psychiatry, University of Sheffield, The Longley Centre, Norwood Grange Drive, Sheffield S5 7JT, UK – sequence: 3 givenname: Randolph W. surname: Parks fullname: Parks, Randolph W. organization: Sheffield Cognition and Neuroimaging Laboratory (SCANLab), Academic Clinical Psychiatry, University of Sheffield, The Longley Centre, Norwood Grange Drive, Sheffield S5 7JT, UK – sequence: 4 givenname: Hector surname: Accosta-Mesa fullname: Accosta-Mesa, Hector organization: Department of Psychology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK – sequence: 5 givenname: Claire surname: Young fullname: Young, Claire organization: Sheffield Care Trust, The Longley Centre, Norwood Grange Drive, Sheffield S5 7JT, UK – sequence: 6 givenname: Iain D. surname: Wilkinson fullname: Wilkinson, Iain D. organization: Academic Unit of Radiology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK – sequence: 7 givenname: Michael D. surname: Hunter fullname: Hunter, Michael D. organization: Sheffield Cognition and Neuroimaging Laboratory (SCANLab), Academic Clinical Psychiatry, University of Sheffield, The Longley Centre, Norwood Grange Drive, Sheffield S5 7JT, UK – sequence: 8 givenname: Peter W.R. surname: Woodruff fullname: Woodruff, Peter W.R. organization: Sheffield Cognition and Neuroimaging Laboratory (SCANLab), Academic Clinical Psychiatry, University of Sheffield, The Longley Centre, Norwood Grange Drive, Sheffield S5 7JT, UK |
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Keywords | Depth perception Magnetic resonance imaging Normal aging Memory Human Nervous system diseases Senescence Healthy subject Alzheimer disease Space perception Nuclear magnetic resonance imaging Depth Cerebral disorder Vision Central nervous system disease Medical imagery Degenerative disease Elderly Functional imaging |
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Snippet | The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in patients... Abstract The neural basis of visuospatial deficits in Alzheimer's disease is unclear. We wished to investigate the neural basis of visuospatial perception in... |
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SubjectTerms | Adult and adolescent clinical studies Aged Aged, 80 and over Alzheimer Disease - diagnosis Alzheimer Disease - physiopathology Biological and medical sciences Brain - physiopathology Cognition Disorders - diagnosis Cognition Disorders - physiopathology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Depth perception Depth Perception - physiology Female Humans Magnetic Resonance Imaging Male Medical sciences Memory Motion Perception - physiology Neurology Neuropsychological Tests Normal aging Organic mental disorders. Neuropsychology Orientation - physiology Oxygen - blood Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Radiology Space Perception - physiology Task Performance and Analysis Visual Perception - physiology |
Title | The neural basis of visuospatial perception in Alzheimer's disease and healthy elderly comparison subjects: An fMRI study |
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