Patterns of atrophy differ among specific subtypes of mild cognitive impairment. 2007

Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
Department of Radiology, Mayo Clinic, Rochester, Minnesota 55905, USA.

BACKGROUND In most patients, mild cognitive impairment (MCI) represents the clinically evident prodromal phase of dementia. This is most well established in amnestic MCI, which is most commonly a precursor to Alzheimer disease (AD). It follows, however, that subjects with MCI who have impairment in nonmemory domains may progress to non-AD degenerative dementias. OBJECTIVE To investigate patterns of cerebral atrophy associated with specific subtypes of MCI. METHODS Case-control study. METHODS Community-based sample at a tertiary referral center. METHODS One hundred forty-five subjects with MCI and 145 age- and sex-matched cognitively normal control subjects. Mild cognitive impairment was classified as amnestic, single cognitive domain; amnestic, multiple domain; nonamnestic, single domain; and nonamnestic, multiple domain. Subjects with nonamnestic single-domain MCI were classified into language, attention/executive, and visuospatial subgroups on the basis of specific cognitive impairment. METHODS Patterns of gray matter loss in the MCI groups compared with control subjects, assessed using voxel-based morphometry. RESULTS Subjects in the amnestic single- and multiple-domain groups showed loss in the medial and inferior temporal lobes compared with control subjects, and those in the multiple-domain group also had involvement of the posterior temporal lobe, parietal association cortex, and posterior cingulate. Subjects in the nonamnestic single-domain group with language impairment showed loss in the left anterior inferior temporal lobe. The group with attention/executive deficits showed loss in the basal forebrain and hypothalamus. No coherent patterns of loss were observed in the other subgroups. CONCLUSIONS The pattern of atrophy in the amnestic MCI groups is consistent with the concept that MCI in most of these subjects represents prodromal AD. However, the varying patterns in the language and attention/executive subgroups suggest that these subjects may have a different underlying disorder.

UI MeSH Term Description Entries
D007802 Language A verbal or nonverbal means of communicating ideas or feelings. Dialect,Dialects,Languages
D008279 Magnetic Resonance Imaging Non-invasive method of demonstrating internal anatomy based on the principle that atomic nuclei in a strong magnetic field absorb pulses of radiofrequency energy and emit them as radiowaves which can be reconstructed into computerized images. The concept includes proton spin tomographic techniques. Chemical Shift Imaging,MR Tomography,MRI Scans,MRI, Functional,Magnetic Resonance Image,Magnetic Resonance Imaging, Functional,Magnetization Transfer Contrast Imaging,NMR Imaging,NMR Tomography,Tomography, NMR,Tomography, Proton Spin,fMRI,Functional Magnetic Resonance Imaging,Imaging, Chemical Shift,Proton Spin Tomography,Spin Echo Imaging,Steady-State Free Precession MRI,Tomography, MR,Zeugmatography,Chemical Shift Imagings,Echo Imaging, Spin,Echo Imagings, Spin,Functional MRI,Functional MRIs,Image, Magnetic Resonance,Imaging, Magnetic Resonance,Imaging, NMR,Imaging, Spin Echo,Imagings, Chemical Shift,Imagings, Spin Echo,MRI Scan,MRIs, Functional,Magnetic Resonance Images,Resonance Image, Magnetic,Scan, MRI,Scans, MRI,Shift Imaging, Chemical,Shift Imagings, Chemical,Spin Echo Imagings,Steady State Free Precession MRI
D008297 Male Males
D001921 Brain The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM. Encephalon
D003072 Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. Overinclusion,Disorder, Cognition,Disorders, Cognition
D003704 Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness. Senile Paranoid Dementia,Amentia,Familial Dementia,Amentias,Dementia, Familial,Dementias,Dementias, Familial,Dementias, Senile Paranoid,Familial Dementias,Paranoid Dementia, Senile,Paranoid Dementias, Senile,Senile Paranoid Dementias
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D000369 Aged, 80 and over Persons 80 years of age and older. Oldest Old

Related Publications

Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
April 2012, Journal of the neurological sciences,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
November 2016, Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
April 2021, Nutrients,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
January 2008, Dementia and geriatric cognitive disorders,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
January 2008, The open neuroimaging journal,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
January 2006, Archives of neurology,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
September 2010, Human brain mapping,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
April 1995, Alcoholism, clinical and experimental research,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
January 2016, Applied neuropsychology. Adult,
Jennifer L Whitwell, and Ronald C Petersen, and Selamawit Negash, and Stephen D Weigand, and Kejal Kantarci, and Robert J Ivnik, and David S Knopman, and Bradley F Boeve, and Glenn E Smith, and Clifford R Jack
March 2021, Journal of clinical and experimental neuropsychology,
Copied contents to your clipboard!