Corpus callosum atrophy is a possible indicator of region- and cell type-specific neuronal degeneration in Alzheimer disease: a magnetic resonance imaging analysis.

BACKGROUND Pathological studies in Alzheimer disease indicate the specific loss of layer III and V large pyramidal neurons in association cortex. These neurons give rise to long corticocortical connections within and between the cerebral hemispheres. OBJECTIVE To evaluate the corpus callosum as an in vivo marker for cortical neuronal loss. METHOD Using a new imaging technique, we measured region-specific corpus callosum atrophy in patients with Alzheimer disease and correlated the changes with neuropsychological functioning. Total cross-sectional area of the corpus callosum and areas of 5 callosal subregions were measured on midsagittal magnetic resonance imaging scans of 14 patients with Alzheimer disease (mean age, 64.4 years; Mini-Mental State Examination score, 11.4) and 22 healthy age- and sex-matched control subjects (mean age, 66.6 years; Mini-Mental State Examination score, 29.8). All subjects had minimal white matter changes. RESULTS The total callosal area was significantly reduced in the patients with Alzheimer disease, with the greatest changes in the rostrum and splenium and relative sparing of the callosal body. Regional callosal atrophy correlated significantly with cognitive impairment in the patients with Alzheimer disease, but not with age or the white matter hyperintensities score. CONCLUSIONS Callosal atrophy in patients with Alzheimer disease with only minimal white matter changes may indicate loss of callosal efferent neurons in corresponding regions of the cortex. Because these neurons are a subset of corticocortical projecting neurons, region-specific callosal atrophy may serve as a marker of progressive neocortical disconnection in Alzheimer disease.

[1]  Ruth A. Carper,et al.  Atrophy of the Corpus Callosum in Alzheimer's Disease Versus Healthy Aging , 1996, Journal of the American Geriatrics Society.

[2]  R. Armstrong The spatial pattern of discrete beta-amyloid deposits in Alzheimer's disease reflects synaptic disconnection. , 1996, Dementia.

[3]  F. Conti,et al.  The neurotransmitters and postsynaptic actions of callosally projecting neurons , 1994, Behavioural Brain Research.

[4]  B. C. Richardson,et al.  Human corpus callosum in aging and alzheimer's disease: a magnetic resonance imaging study , 1994, Neurobiology of Aging.

[5]  H. Fukuyama,et al.  Callosal atrophy parallels decreased cortical oxygen metabolism and neuropsychological impairment in Alzheimer's disease. , 1993, Archives of neurology.

[6]  C. Cuénod,et al.  Amygdala atrophy in Alzheimer's disease. An in vivo magnetic resonance imaging study. , 1993, Archives of neurology.

[7]  P. Scheltens,et al.  A semiquantative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging , 1993, Journal of the Neurological Sciences.

[8]  J. Talairach,et al.  Referentially oriented cerebral MRI anatomy : an atlas of stereotaxic anatomical correlations for gray and white matter , 1993 .

[9]  P. Scheltens,et al.  White matter lesions on magnetic resonance imaging in clinically diagnosed Alzheimer's disease. Evidence for heterogeneity. , 1992, Brain : a journal of neurology.

[10]  C. Grady,et al.  Cerebral Metabolism in Aging and Dementia , 1992 .

[11]  Z. Wang,et al.  Localization of functional projections from corpus callosum to cerebral cortex. , 1991, Chinese medical journal.

[12]  C. Pozzilli,et al.  Anterior Corpus Callosum Atrophy and Verbal Fluency in Multiple Sclerosis , 1991, Cortex.

[13]  J. Taveras,et al.  Abnormal corpus callosum: a sensitive and specific indicator of multiple sclerosis. , 1991, Radiology.

[14]  K. Jellinger,et al.  Morphometry of the corpus callosum in normal aging and Alzheimer's disease. , 1991, Journal of neural transmission. Supplementum.

[15]  The dissection by Alzheimer's disease of cortical and limbic neural systems relevant to memory , 1990 .

[16]  J. Mazziotta,et al.  [18F]-fluorodeoxyglucose (FDG) and positron emission tomography (PET) in aging and dementia. A decade of studies. , 1989, European neurology.

[17]  J. Trojanowski,et al.  Brain MR: pathologic correlation with gross and histopathology. 2. Hyperintense white-matter foci in the elderly. , 1988, AJR. American journal of roentgenology.

[18]  J. Trojanowski,et al.  Brain MR: pathologic correlation with gross and histopathology. 1. Lacunar infarction and Virchow-Robin spaces. , 1988, AJR. American journal of roentgenology.

[19]  J H Simon,et al.  Quantitative determination of MS-induced corpus callosum atrophy in vivo using MR imaging. , 1987, AJNR. American journal of neuroradiology.

[20]  M J Campbell,et al.  Laminar and regional distributions of neurofibrillary tangles and neuritic plaques in Alzheimer's disease: a quantitative study of visual and auditory cortices , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  L A Hayman,et al.  White-matter lesions in MR imaging of clinically healthy brains of elderly subjects: possible pathologic basis. , 1987, Radiology.

[22]  R F Spetzler,et al.  Incidental subcortical lesions identified on magnetic resonance imaging in the elderly. II. Postmortem pathological correlations. , 1986, Stroke.

[23]  G. Innocenti General Organization of Callosal Connections in the Cerebral Cortex , 1986 .

[24]  E. Ross,et al.  Topography of the Human Corpus Callosum , 1985, Journal of neuropathology and experimental neurology.

[25]  J. Morrison,et al.  Quantitative morphology and regional and laminar distributions of senile plaques in Alzheimer's disease , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  G K Wilcock,et al.  Anatomical correlates of the distribution of the pathological changes in the neocortex in Alzheimer disease. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[27]  M. Folstein,et al.  Clinical diagnosis of Alzheimer's disease , 1984, Neurology.

[28]  J. Tigges,et al.  Areal and laminar distribution of neurons interconnecting the central visual cortical areas 17, 18, 19, and MT in squirrel monkey (Saimiri) , 1981, The Journal of comparative neurology.

[29]  T. Yin,et al.  Homotopic and heterotopic callosal afferents of caudal inferior parietal lobule in Macaca mulatta , 1981, The Journal of comparative neurology.

[30]  John Q. Trojanowski,et al.  Prefrontal granular cortex of the rhesus monkey. I. Intrahemispheric cortical afferents , 1977, Brain Research.

[31]  J J Bartko,et al.  ON THE METHODS AND THEORY OF RELIABILITY , 1976, The Journal of nervous and mental disease.

[32]  D. Whitteridge,et al.  Degeneration of layer III pyramidal cells in area 18 following destruction of callosal input , 1976, Brain Research.

[33]  S. Folstein,et al.  "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.

[34]  J. Trojanowski,et al.  The cells of origin of the corpus callosum in rat, cat and rhesus monkey. , 1974, Brain research.

[35]  D. Pandya,et al.  The topographical distribution of interhemispheric projections in the corpus callosum of the rhesus monkey. , 1971, Brain research.

[36]  S. Sunderland THE DISTRIBUTION OF COMMISSURAL FIBRES IN THE CORPUS CALLOSUM IN THE MACAQUE MONKEY , 1940, Journal of neurology and psychiatry.