The cortical neuroanatomy of neuropsychological deficits in mild cognitive impairment and Alzheimer's disease: A surface-based morphometric analysis
► There are different patterns of cortical thinning associated with neuropsychological tests. ► The neuropsychological tests have a hemispheric laterality associated with each functions. ► The patterns of cortical thinning are pathological markers for cognitive dysfunction. Patients with probable Al...
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Published in | Neuropsychologia Vol. 49; no. 14; pp. 3931 - 3945 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Kidlington
Elsevier Ltd
01.12.2011
Elsevier |
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Online Access | Get full text |
ISSN | 0028-3932 1873-3514 1873-3514 |
DOI | 10.1016/j.neuropsychologia.2011.10.010 |
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Abstract | ► There are different patterns of cortical thinning associated with neuropsychological tests. ► The neuropsychological tests have a hemispheric laterality associated with each functions. ► The patterns of cortical thinning are pathological markers for cognitive dysfunction.
Patients with probable Alzheimer's disease (AD) and the amnesic form of mild cognitive impairment (aMCI) often demonstrate several types of neuropsychological deficits. These deficits are often related to cortical atrophy, induced by neuronal degradation. The purpose of this study is to investigate whether different anatomic patterns of cortical atrophy are associated with specific neuropsychological deficits. The participants were 170 patients with AD and 99 patients with aMCI. All participants underwent the Seoul Neuropsychological Screening Battery (SNSB), which includes tests that assess attention, language, visuospatial functions, verbal and visual memory, and frontal/executive functions. Cortical atrophy (thinning) was quantified by measuring the thickness of the cortical mantle across the entire brain using automated, three-dimensional magnetic resonance imaging. The relationship between cortical thickness and neuropsychological performance was analysed using stepwise multiple linear regression analyses. These analyses (corrected P<.001) showed that several specific brain regions with cortical thinning were associated with cognitive dysfunction including: digit span backward, verbal and picture recall, naming and fluency, drawing–copying, response inhibition and selective attention. Some of the other functions, however, were not associated with specific foci of cortical atrophy (digit span forward, the word reading portion of the Stroop test, word and picture recognition). Our study, involving a large sample of participants with aMCI and AD, provides support for the postulate that cortical thinning-atrophy in specific anatomic loci are pathological markers for specific forms of cognitive dysfunction. |
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AbstractList | Patients with probable Alzheimer's disease (AD) and the amnesic form of mild cognitive impairment (aMCI) often demonstrate several types of neuropsychological deficits. These deficits are often related to cortical atrophy, induced by neuronal degradation. The purpose of this study is to investigate whether different anatomic patterns of cortical atrophy are associated with specific neuropsychological deficits. The participants were 170 patients with AD and 99 patients with aMCI. All participants underwent the Seoul Neuropsychological Screening Battery (SNSB), which includes tests that assess attention, language, visuospatial functions, verbal and visual memory, and frontal/executive functions. Cortical atrophy (thinning) was quantified by measuring the thickness of the cortical mantle across the entire brain using automated, three-dimensional magnetic resonance imaging. The relationship between cortical thickness and neuropsychological performance was analysed using stepwise multiple linear regression analyses. These analyses (corrected P<.001) showed that several specific brain regions with cortical thinning were associated with cognitive dysfunction including: digit span backward, verbal and picture recall, naming and fluency, drawing-copying, response inhibition and selective attention. Some of the other functions, however, were not associated with specific foci of cortical atrophy (digit span forward, the word reading portion of the Stroop test, word and picture recognition). Our study, involving a large sample of participants with aMCI and AD, provides support for the postulate that cortical thinning-atrophy in specific anatomic loci are pathological markers for specific forms of cognitive dysfunction. ► There are different patterns of cortical thinning associated with neuropsychological tests. ► The neuropsychological tests have a hemispheric laterality associated with each functions. ► The patterns of cortical thinning are pathological markers for cognitive dysfunction. Patients with probable Alzheimer's disease (AD) and the amnesic form of mild cognitive impairment (aMCI) often demonstrate several types of neuropsychological deficits. These deficits are often related to cortical atrophy, induced by neuronal degradation. The purpose of this study is to investigate whether different anatomic patterns of cortical atrophy are associated with specific neuropsychological deficits. The participants were 170 patients with AD and 99 patients with aMCI. All participants underwent the Seoul Neuropsychological Screening Battery (SNSB), which includes tests that assess attention, language, visuospatial functions, verbal and visual memory, and frontal/executive functions. Cortical atrophy (thinning) was quantified by measuring the thickness of the cortical mantle across the entire brain using automated, three-dimensional magnetic resonance imaging. The relationship between cortical thickness and neuropsychological performance was analysed using stepwise multiple linear regression analyses. These analyses (corrected P<.001) showed that several specific brain regions with cortical thinning were associated with cognitive dysfunction including: digit span backward, verbal and picture recall, naming and fluency, drawing–copying, response inhibition and selective attention. Some of the other functions, however, were not associated with specific foci of cortical atrophy (digit span forward, the word reading portion of the Stroop test, word and picture recognition). Our study, involving a large sample of participants with aMCI and AD, provides support for the postulate that cortical thinning-atrophy in specific anatomic loci are pathological markers for specific forms of cognitive dysfunction. Patients with probable Alzheimer's disease (AD) and the amnesic form of mild cognitive impairment (aMCI) often demonstrate several types of neuropsychological deficits. These deficits are often related to cortical atrophy, induced by neuronal degradation. The purpose of this study is to investigate whether different anatomic patterns of cortical atrophy are associated with specific neuropsychological deficits. The participants were 170 patients with AD and 99 patients with aMCI. All participants underwent the Seoul Neuropsychological Screening Battery (SNSB), which includes tests that assess attention, language, visuospatial functions, verbal and visual memory, and frontal/executive functions. Cortical atrophy (thinning) was quantified by measuring the thickness of the cortical mantle across the entire brain using automated, three-dimensional magnetic resonance imaging. The relationship between cortical thickness and neuropsychological performance was analysed using stepwise multiple linear regression analyses. These analyses (corrected P<.001) showed that several specific brain regions with cortical thinning were associated with cognitive dysfunction including: digit span backward, verbal and picture recall, naming and fluency, drawing-copying, response inhibition and selective attention. Some of the other functions, however, were not associated with specific foci of cortical atrophy (digit span forward, the word reading portion of the Stroop test, word and picture recognition). Our study, involving a large sample of participants with aMCI and AD, provides support for the postulate that cortical thinning-atrophy in specific anatomic loci are pathological markers for specific forms of cognitive dysfunction.Patients with probable Alzheimer's disease (AD) and the amnesic form of mild cognitive impairment (aMCI) often demonstrate several types of neuropsychological deficits. These deficits are often related to cortical atrophy, induced by neuronal degradation. The purpose of this study is to investigate whether different anatomic patterns of cortical atrophy are associated with specific neuropsychological deficits. The participants were 170 patients with AD and 99 patients with aMCI. All participants underwent the Seoul Neuropsychological Screening Battery (SNSB), which includes tests that assess attention, language, visuospatial functions, verbal and visual memory, and frontal/executive functions. Cortical atrophy (thinning) was quantified by measuring the thickness of the cortical mantle across the entire brain using automated, three-dimensional magnetic resonance imaging. The relationship between cortical thickness and neuropsychological performance was analysed using stepwise multiple linear regression analyses. These analyses (corrected P<.001) showed that several specific brain regions with cortical thinning were associated with cognitive dysfunction including: digit span backward, verbal and picture recall, naming and fluency, drawing-copying, response inhibition and selective attention. Some of the other functions, however, were not associated with specific foci of cortical atrophy (digit span forward, the word reading portion of the Stroop test, word and picture recognition). Our study, involving a large sample of participants with aMCI and AD, provides support for the postulate that cortical thinning-atrophy in specific anatomic loci are pathological markers for specific forms of cognitive dysfunction. |
Author | Lee, Byung Hwa Lee, Jun Hong Chin, Juhee Im, Kiho Lee, Jong-Min Seo, Sang Won Ahn, Hyun-Jung Na, Duk L. Suh, Mee Kyung Kim, Sung Tae Heilman, Kenneth M. |
Author_xml | – sequence: 1 givenname: Hyun-Jung surname: Ahn fullname: Ahn, Hyun-Jung organization: Department of Neurology, Dementia Center, Ilsan Hospital, National Health Insurance Corporation, Goyang, South Korea – sequence: 2 givenname: Sang Won surname: Seo fullname: Seo, Sang Won organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea – sequence: 3 givenname: Juhee surname: Chin fullname: Chin, Juhee organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea – sequence: 4 givenname: Mee Kyung surname: Suh fullname: Suh, Mee Kyung organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea – sequence: 5 givenname: Byung Hwa surname: Lee fullname: Lee, Byung Hwa organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea – sequence: 6 givenname: Sung Tae surname: Kim fullname: Kim, Sung Tae organization: Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea – sequence: 7 givenname: Kiho surname: Im fullname: Im, Kiho organization: Division of Newborn Medicine, Children's Hospital Boston, Harvard Medical School, Boston, MA, USA – sequence: 8 givenname: Jong-Min surname: Lee fullname: Lee, Jong-Min organization: Department of Biomedical Engineering, Hanyang University, Seoul, South Korea – sequence: 9 givenname: Jun Hong surname: Lee fullname: Lee, Jun Hong organization: Department of Neurology, Dementia Center, Ilsan Hospital, National Health Insurance Corporation, Goyang, South Korea – sequence: 10 givenname: Kenneth M. surname: Heilman fullname: Heilman, Kenneth M. organization: Department of Neurology, University of Florida and Veterans Affairs Medical Center, Gainesville, FL, USA – sequence: 11 givenname: Duk L. surname: Na fullname: Na, Duk L. email: dukna@skku.edu organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea |
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Keywords | Cognition Neuropsychological tests Mild cognitive impairment Alzheimer's disease Cortical atrophy Human Nervous system diseases Cerebral cortex Cognitive disorder Alzheimer disease Central nervous system Neuropsychological test Psychometrics Encephalon Cerebral disorder Atrophy Central nervous system disease Degenerative disease mild cognitive impairment Morphometry |
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Snippet | ► There are different patterns of cortical thinning associated with neuropsychological tests. ► The neuropsychological tests have a hemispheric laterality... Patients with probable Alzheimer's disease (AD) and the amnesic form of mild cognitive impairment (aMCI) often demonstrate several types of neuropsychological... |
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SubjectTerms | Adult and adolescent clinical studies Aged Aged, 80 and over Alzheimer Disease - complications Alzheimer Disease - pathology Alzheimer's disease Biological and medical sciences Brain Mapping Cerebral Cortex - pathology Cerebral Cortex - physiopathology Cognition Cognitive Dysfunction - etiology Cognitive Dysfunction - pathology Cortical atrophy Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dissociative Disorders Female Functional Laterality Geriatrics Humans Image Processing, Computer-Assisted Magnetic Resonance Imaging Male Medical sciences Middle Aged Mild cognitive impairment Neurology Neuropsychological Tests Organic mental disorders. Neuropsychology Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Statistics as Topic |
Title | The cortical neuroanatomy of neuropsychological deficits in mild cognitive impairment and Alzheimer's disease: A surface-based morphometric analysis |
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