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 inNeuropsychologia Vol. 49; no. 14; pp. 3931 - 3945
Main Authors Ahn, Hyun-Jung, Seo, Sang Won, Chin, Juhee, Suh, Mee Kyung, Lee, Byung Hwa, Kim, Sung Tae, Im, Kiho, Lee, Jong-Min, Lee, Jun Hong, Heilman, Kenneth M., Na, Duk L.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.12.2011
Elsevier
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Online AccessGet full text
ISSN0028-3932
1873-3514
1873-3514
DOI10.1016/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.
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.
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  organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea
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  fullname: Lee, Jong-Min
  organization: Department of Biomedical Engineering, Hanyang University, Seoul, South Korea
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  fullname: Lee, Jun Hong
  organization: Department of Neurology, Dementia Center, Ilsan Hospital, National Health Insurance Corporation, Goyang, South Korea
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  givenname: Kenneth M.
  surname: Heilman
  fullname: Heilman, Kenneth M.
  organization: Department of Neurology, University of Florida and Veterans Affairs Medical Center, Gainesville, FL, USA
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  givenname: Duk L.
  surname: Na
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  email: dukna@skku.edu
  organization: Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea
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IsPeerReviewed true
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Issue 14
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
Language English
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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
URI https://dx.doi.org/10.1016/j.neuropsychologia.2011.10.010
https://www.ncbi.nlm.nih.gov/pubmed/22019776
https://www.proquest.com/docview/905961698
Volume 49
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