Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-xbtfd Total loading time: 0 Render date: 2024-11-11T08:25:25.112Z Has data issue: false hasContentIssue false

27 - Neuroimaging of other dementing disorders

from Section IV - Cognitive Disorders

Published online by Cambridge University Press:  10 January 2011

William Hu
Affiliation:
Department of Neurology University of Pennsylvania School of Medicine Philadelphia, PA, USA
Murray Grossman
Affiliation:
Department of Neurology University of Pennsylvania School of Medicine Philadelphia, PA, USA
Martha E. Shenton
Affiliation:
VA Boston Healthcare System and Brigham and Women's Hospital, Harvard Medical School
Bruce I. Turetsky
Affiliation:
University of Pennsylvania
Get access

Summary

Introduction

Alzheimer's disease (AD) is the most common form of dementing illness in the elderly (Kokmen et al.,1993), but advances in molecular pathology over the past few decades have led to the identification of other common neurodegenerative disorders (Prusiner and Hsiao, 1994; Neary et al., 1998; McKhann et al., 2001; Boeve et al., 2003; Lippa et al., 2007; Murray et al., 2007). Patients with these non-Alzheimer dementia disorders frequently have similar subjective complaints as patients with AD, but atypical features in the evaluation of these cognitively impaired patients should alert the astute physician of an alternative non-AD diagnosis, including behavioral and language variants of frontotemporal dementia (Neary et al., 1998; McKhann et al., 2001), dementia with Lewy bodies (Lippa et al., 2007), vascular dementia, and other forms of less common neurological disorders, including Creutzfeldt–Jakob disease (Prusiner and Hsiao, 1994). The utility of imaging studies has been studied extensively in many of these disorders, and this chapter will focus on the group differences between disorders and highlight the role of structural and functional imaging in non-Alzheimer dementias. Disease-specific features unique to one type or one group of disorders are frequently congruent with the localization model of neurodegenerative disease based on prominent clinical deficits, but the majority of these studies lack the power to determine the positive and negative predictive values of disease-specific features at the group level when used on an individual patient basis, despite variable amount of anecdotal clinical evidence.

Type
Chapter
Information
Understanding Neuropsychiatric Disorders
Insights from Neuroimaging
, pp. 371 - 394
Publisher: Cambridge University Press
Print publication year: 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aarsland, D, Litvan, I, Salmon, D, et al. 2003. Performance on the dementia rating scale in Parkinson's disease with dementia and dementia with Lewy bodies: Comparison with progressive supranuclear palsy and Alzheimer's disease. J Neurol Neurosurg Psychiatry 74, 1215–20.Google Scholar
Amador-Ortiz, C and Dickson, D W. 2008. Neuropathology of hippocampal sclerosis. Handb Clin Neurol 89, 569–72.Google Scholar
Apaydin, H, Ahlskog, J E, Parisi, J E, et al. 2002. Parkinson disease neuropathology: Later-developing dementia and loss of the levodopa response. Arch Neurol 59, 102–12.Google Scholar
Ash, S, Moore, P, Vesely, L, et al. 2009. Non-fluent speech in frontotemporal lobar degeneration. J Neuroling 22, 370–83.Google Scholar
Asmuth, J, Zhang, H, Vesely, L, et al. 2008. DTI analysis of white matter deficits in frontotemporal lobar dementia. Neurology 70, A452.Google Scholar
Ballard, C, Ziabreva, I, Perry, R, et al. 2006. Differences in neuropathologic characteristics across the Lewy body dementia spectrum. Neurology 67, 1931–4.Google Scholar
Ballmaier, M, O'Brien, J T, Burton, E J, et al. 2004. Comparing gray matter loss profiles between dementia with Lewy bodies and Alzheimer's disease using cortical pattern matching: diagnosis and gender effects. Neuroimage 23, 325–35.Google Scholar
Barber, R, Ballard, C, McKeith, I G, et al. 2000. MRI volumetric study of dementia with Lewy bodies: A comparison with AD and vascular dementia. Neurology 54, 1304–9.Google Scholar
Beck, J, Rohrer, J D, Campbell, T, et al. 2008. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain 131, 706–20.Google Scholar
Bersano, A, Del Bo, R, Lamperti, C, et al. 2007. Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation. Neurobiol Aging 30, 752–8.Google Scholar
Beyer, M K, Larsen, J P, Aasrland, D, et al. 2007. Gray matter atrophy in Parkinson disease with dementia and dementia with Lewy bodies. Neurology 69, 747–54.Google Scholar
Bian, H, Swieten, J C, Leight, S, et al. 2008. CSF biomarkers in frontotemporal lobar degeneration with known pathology. Neurology 70, 1827–35.Google Scholar
Blin, J, Vidailhet, M J, Pillon, B, et al. 1992. Corticobasal degeneration: Decreased and asymmetrical glucose consumption as studied with PET. Mov Disord 7, 348–54.Google Scholar
Boeve, B F, Lang, A E, Litvan, I, et al. 2003. Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia. Ann Neurol 54 (Suppl 5), S15–9.Google Scholar
Bonelli, S B, Ransmayr, G, Steffelbauer, M, et al. 2004. L-dopa responsiveness in dementia with Lewy bodies, Parkinson disease with and without dementia. Neurology 63, 376–8.Google Scholar
Borroni, B, Brambati, S M, Agosti, C, et al. 2007. Evidence of white matter changes on diffusion tensor imaging in frontotemporal dementia. Arch Neurol 64, 246–51.Google Scholar
Boxer, A L, Geschwind, M D, Belfor, N, et al. 2006. Patterns of brain atrophy that differentiate corticobasal degeneration syndrome from progressive supranuclear palsy. Arch Neurol 63, 81–6.Google Scholar
Bright, P, Moss, H E, Stamatakis, E A, et al. 2008. Longitudinal studies of semantic dementia: The relationship between structural and functional changes over time. Neuropsychologia 46, 2177–88.Google Scholar
Burn, D J, Rowan, E N, Minett, T, et al. 2003. Extrapyramidal features in Parkinson's disease with and without dementia and dementia with Lewy bodies: A cross-sectional comparative study. Mov Disord 18, 884–9.Google Scholar
Burton, E J, Karas, G, Paling, S M, et al. 2002. Patterns of cerebral atrophy in dementia with Lewy bodies using voxel-based morphometry. Neuroimage 17, 618–30.Google Scholar
Burton, E J, McKeith, I G, Burn, D J, et al. 2004. Cerebral atrophy in Parkinson's disease with and without dementia: A comparison with Alzheimer's disease, dementia with Lewy bodies and controls. Brain 127, 791–800.Google Scholar
Buxbaum, L J, Kyle, K, Grossman, M, et al. 2007. Left inferior parietal representations for skilled hand-object interactions: Evidence from stroke and corticobasal degeneration. Cortex 43, 411–23.Google Scholar
Caselli, R J, Jack, C R, Petersen, R C, et al. 1992. Asymmetric cortical degenerative syndromes: Clinical and radiologic correlations. Neurology 42, 1462–8.Google Scholar
Chang, J L, Lomen-Hoerth, C, Murphy, C J, et al. 2005. A voxel-based morphometry study of patterns of brain atrophy in ALS and ALS/FTLD. Neurology 65, 75–80.Google Scholar
Chao, L L, Schuff, N, Clevenger, E M, et al. 2007. Patterns of white matter atrophy in frontotemporal lobar degeneration. Arch Neurol 64, 1619–24.Google Scholar
Chow, T W, Binns, M A, Freedman, M, et al. 2008. Overlap in frontotemporal atrophy between normal aging and patients with frontotemporal dementias. Alzheimer Dis Assoc Disord 22, 327–35.Google Scholar
Chui, H C, Zarow, C, Mack, W J, et al. 2006. Cognitive impact of subcortical vascular and Alzheimer's disease pathology. Ann Neurol 60, 677–87.Google Scholar
Clark, D G, Charuvastra, A, Miller, B L, et al. 2005. Fluent versus nonfluent primary progressive aphasia: A comparison of clinical and functional neuroimaging features. Brain Lang 94, 54–60.Google Scholar
Colloby, S J, O'Brien, J T, Fenwick, J D, et al. 2004. The application of statistical parametric mapping to 123I-FP-CIT SPECT in dementia with Lewy bodies, Alzheimer's disease and Parkinson's disease. Neuroimage 23, 956–66.Google Scholar
Colloby, S J, Pakrasi, S, Firbank, M J, et al. 2006. In vivo SPECT imaging of muscarinic acetylcholine receptors using (R, R) 123I-QNB in dementia with Lewy bodies and Parkinson's disease dementia. Neuroimage 33, 423–9.Google Scholar
Colloby, S J, Williams, E D, Burn, D J, et al. 2005. Progression of dopaminergic degeneration in dementia with Lewy bodies and Parkinson's disease with and without dementia assessed using 123I-FP-CIT SPECT. Eur J Nucl Med Mol Imaging 32, 1176–85.Google Scholar
Colosimo, C, Hughes, A J, Kilford, L, et al. 2003. Lewy body cortical involvement may not always predict dementia in Parkinson's disease. J Neurol Neurosurg Psychiatry 74, 852–6.Google Scholar
Cooke, A, DeVita, C, Gee, J, et al. 2003. Neural basis for sentence comprehension deficits in frontotemporal dementia. Brain Lang 85, 211–21.Google Scholar
Davatzikos, C, Resnick, S M, Wu, X, et al. 2008. Individual patient diagnosis of AD and FTD via high-dimensional pattern classification of MRI. Neuroimage 41, 1220–7.Google Scholar
Davies, R R, Halliday, G M, Xuereb, J H, et al. 2008. The neural basis of semantic memory: Evidence from semantic dementia. Neurobiol Aging 30, 2043–52.Google Scholar
DeCarli, C, Massaro, J, Harvey, D, et al. 2005. Measures of brain morphology and infarction in the Framingham heart study: Establishing what is normal. Neurobiol Aging 26, 491–510.Google Scholar
Delano-Wood, L, Abeles, N, Sacco, J M, et al. 2008. Regional white matter pathology in mild cognitive impairment: Differential influence of lesion type on neuropsychological functioning. Stroke 39, 794–9.Google Scholar
Desgranges, B, Matuszewski, V, Poilino, P, et al. 2007. Anatomical and functional alterations in semantic dementia: A voxel-based MRI and PET study. Neurobiol Aging 28, 1904–13.Google Scholar
Dickson, D W. 2001. Neuropathology of Pick's disease. Neurology 56 (11 Suppl 4), S16–20.Google Scholar
Dickson, D W. 2008. Neuropathology of progressive supranuclear palsy. Handb Clin Neurol 89, 487–91.Google Scholar
Dickson, D W, Bergeron, C, Chin, S S, et al. 2002. Office of Rare Diseases neuropathologic criteria for corticobasal degeneration. J Neuropathol Exp Neurol 61, 935–46.Google Scholar
Donnemiller, E, Heilmann, J, Wenning, G K, et al. 1997. Brain perfusion scintigraphy with 99mTc-HMPAO or 99mTc-ECD and 123I-beta-CIT single-photon emission tomography in dementia of the Alzheimer-type and diffuse Lewy body disease. Eur J Nucl Med 24, 320–5.Google Scholar
Downes, J J, Priestley, N M, Doran, M, et al. 1998. Intellectual, mnemonic, and frontal functions in dementia with Lewy bodies: A comparison with early and advanced Parkinson's disease. Behav Neurol 11, 173–83.Google Scholar
Drzezga, A, Grimmer, T, Henriksen, G, et al. 2008. Imaging of amyloid plaques and cerebral glucose metabolism in semantic dementia and Alzheimer's disease. Neuroimage 39, 619–33.Google Scholar
Eckert, T, Barnes, A, Dhawan, V, et al. 2005. FDG PET in the differential diagnosis of parkinsonian disorders. Neuroimage 26, 912–21.Google Scholar
Eerola, J, Tienari, P J, Kaakkola, S, et al. 2005. How useful is [123I]beta-CIT SPECT in clinical practice? J Neurol Neurosurg Psychiatry 76, 1211–6.Google Scholar
Eidelberg, D, Dhawan, V, Moeller, J R, et al. 1991. The metabolic landscape of cortico-basal ganglionic degeneration: Regional asymmetries studied with positron emission tomography. J Neurol Neurosurg Psychiatry 54, 856–62.Google Scholar
Englund, E. 1998. Neuropathology of white matter changes in Alzheimer's disease and vascular dementia. Dement Geriatr Cogn Disord 9 (Suppl 1), 6–12.Google Scholar
Englund, E. 2002. Neuropathology of white matter lesions in vascular cognitive impairment. Cerebrovasc Dis 13 (Suppl 2), 11–5.Google Scholar
Fagan, A M, Mintun, M A, Mach, R H, et al. 2006. Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid Abeta42 in humans. Ann Neurol 59, 512–9.Google Scholar
Fein, G, Di Sclafani, V, Tanabe, J, et al. 2000. Hippocampal and cortical atrophy predict dementia in subcortical ischemic vascular disease. Neurology 55, 1626–35.Google Scholar
Firbank, M J, Burn, D J, McKeith, I G, et al. 2005. Longitudinal study of cerebral blood flow SPECT in Parkinson's disease with dementia, and dementia with Lewy bodies. Int J Geriatr Psychiatry 20, 776–82.Google Scholar
Firbank, M J, Colloby, S J, Burn, D J, et al. 2003. Regional cerebral blood flow in Parkinson's disease with and without dementia. Neuroimage 20, 1309–19.Google Scholar
Forman, M S, Farmer, J, Johnson, J K, et al. 2006a. Frontotemporal dementia: clinicopathological correlations. Ann Neurol 59, 952–62.Google Scholar
Forman, M S, Mackenzie, I R, Cairns, N J, et al. 2006b. Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. J Neuropathol Exp Neurol 65, 571–81.Google Scholar
Foster, N L, Heidebrink, J L, Clark, C M, et al. 2007. FDG-PET improves accuracy in distinguishing frontotemporal dementia and Alzheimer's disease. Brain 130, 2616–35.Google Scholar
Fulbright, R K, Hoffmann, C, Leed, H, et al. 2008. MR imaging of familial Creutzfeldt-Jakob disease: A blinded and controlled study. Am J Neuroradiol 29, 1638–43.Google Scholar
Garrard, P and Hodges, J R. 2000. Semantic dementia: Clinical, radiological and pathological perspectives. J Neurol 247, 409–22.Google Scholar
Geschwind, M D, Tan, K M, Lennon, V A, et al. 2008. Voltage-gated potassium channel autoimmunity mimicking Creutzfeldt–Jakob disease. Arch Neurol 65, 1341–6.Google Scholar
Geser, F, Winton, M J, Kwong, L K, et al. 2008. Pathological TDP-43 in parkinsonism–dementia complex and amyotrophic lateral sclerosis of Guam. Acta Neuropathol 115, 133–45.Google Scholar
Gold, G, Giannakopoulos, P, Herrmann, F R, et al. 2007. Identification of Alzheimer and vascular lesion thresholds for mixed dementia. Brain 130, 2830–6.Google Scholar
Gorno-Tempini, M L, Brambati, S M, Ginex, V, et al. 2008. The logopenic/phonological variant of primary progressive aphasia. Neurology 71, 1227–34.Google Scholar
Gorno-Tempini, M L, Dronkers, N F, Rankin, K P, et al. 2004. Cognition and anatomy in three variants of primary progressive aphasia. Ann Neurol 55, 335–46.Google Scholar
Gouw, A A, Flier, W M, Fazekas, F, et al. 2008. Progression of white matter hyperintensities and incidence of new lacunes over a 3-year period: The Leukoaraiosis and Disability study. Stroke 39, 1414–20.Google Scholar
Groschel, K, Hauser, T K, Luft, A, et al. 2004. Magnetic resonance imaging-based volumetry differentiates progressive supranuclear palsy from corticobasal degeneration. Neuroimage 21, 714–24.Google Scholar
Grossman, M, Alsop, D, Detre, J A, et al. 2001. Perfusion fMRI using arterial spin labeling in Alzheimer's disease and frontotemporal dementia: Correlations with language. Brain Lang 79, 94–5.Google Scholar
Grossman, M, Cooke, A, DeVita, C, et al. 2002. Sentence processing strategies in healthy seniors with poor comprehension: An fMRI study. Brain Lang 80, 296–313.Google Scholar
Grossman, M, D'Esposito, M, Hughes, E, et al. 1996a. Language comprehension profiles in Alzheimer's disease, multi-infarct dementia, and frontotemporal degeneration. Neurology 47, 183–9.Google Scholar
Grossman, M, McMillan, C, Moore, P, et al. 2004. What's in a name: Voxel-based morphometric analyses of MRI and naming difficulty in Alzheimer's disease, frontotemporal dementia and corticobasal degeneration. Brain 127, 628–49.Google Scholar
Grossman, M, Mickanin, J, Onishi, K, et al. 1996b. Progressive nonfluent aphasia: language, cognitive, and PET measures contrasted to probable Alzheimer's disease. J Cogn Neurosci 8, 135–54.Google Scholar
Grossman, M and Moore, P. 2005. A longitudinal study of sentence comprehension difficulty in primary progressive aphasia. J Neurol Neurosurg Psychiatry 76, 644–9.Google Scholar
Grossman, M, Payer, F, Onishi, K, et al. 1998. Language comprehension and regional cerebral defects in frontotemporal degeneration and Alzheimer's disease. Neurology 50, 157–63.Google Scholar
Grossman, M, Wood, E M, Moore, P, et al. 2007. TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions. Arch Neurol 64, 1449–54.Google Scholar
Grossman, M, Xie, S X, Libon, D J, et al. 2008. Longitudinal decline in autopsy-defined frontotemporal lobar degeneration. Neurology 70, 2036–45.Google Scholar
Gydesen, S, Brown, J M, Brun, A, et al. 2002. Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology 59, 1585–94.Google Scholar
Halpern, C, McMillan, C, Moore, P, et al. 2003. Calculation impairment in neurodegenerative diseases. J Neurol Sci 208, 31–8.Google Scholar
Halpern, C H, Glosser, G, Clark, R, et al. 2004. Dissociation of numbers and objects in corticobasal degeneration and semantic dementia. Neurology 62, 1163–9.Google Scholar
Harding, A J and Halliday, G M. 2001. Cortical Lewy body pathology in the diagnosis of dementia. Acta Neuropathol 102, 355–63.Google Scholar
Hashimoto, M, Kitagaki, H, Imamura, T, et al. 1998. Medial temporal and whole-brain atrophy in dementia with Lewy bodies: A volumetric MRI study. Neurology 51, 357–62.Google Scholar
Higuchi, M, Tashiro, M, Arai, H, et al. 2000. Glucose hypometabolism and neuropathological correlates in brains of dementia with Lewy bodies. Exp Neurol 162, 247–56.Google Scholar
Hodges, J R, Davies, R R, Xuereb, J H, et al. 2004. Clinicopathological correlates in frontotemporal dementia. Ann Neurol 56, 399–406.Google Scholar
Hu, W T, Josephs, K A, Ahlskog, J E, et al. 2005. MRI correlates of alien leg-like phenomenon in corticobasal degeneration. Mov Disord 20, 870–3.Google Scholar
Hu, W T, Josephs, K A, Knopman, D S, et al. 2008. Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease. Acta Neuropathol 116, 215–20.Google Scholar
Hu, W T, Murray, J A, Greenaway, M C, et al. 2006. Cognitive impairment and celiac disease. Arch Neurol 63, 1440–6.Google Scholar
Hu, W T, Rippon, G, Boeve, F, et al. 2009a. Alzheimer disease and corticobasal degeneration presenting as corticobasal syndrome. Mov Disord 24, 1375–9.Google Scholar
Hu, W T, Seelaar, H, Josephs, K A, et al. 2009b. Survival profiles of patients with frontotemporal dementia and motor neuron disease. Arch Neurol 66, 1359–64.Google Scholar
Ishii, K, Imamura, T, Sasaki, M, et al. 1998a. Regional cerebral glucose metabolism in dementia with Lewy bodies and Alzheimer's disease. Neurology 51, 125–30.Google Scholar
Ishii, K, Sakamoto, S, Sasaki, M, et al. 1998b. Cerebral glucose metabolism in patients with frontotemporal dementia. J Nucl Med 39, 1875–8.Google Scholar
Ishii, K, Yamaji, S, Kitagaki, H, et al. 1999. Regional cerebral blood flow difference between dementia with Lewy bodies and AD. Neurology 53, 413–6.Google Scholar
Jellinger, K A and Attems, J. 2007. Neurofibrillary tangle-predominant dementia: Comparison with classical Alzheimer disease. Acta Neuropathol 113, 107–17.Google Scholar
Johnson, J K, Head, E, Kim, R, et al. 1999. Clinical and pathological evidence for a frontal variant of Alzheimer disease. Arch Neurol 56, 1233–9.Google Scholar
Josephs, K A, Duffy, J R, Strand, E A, et al. 2006a. Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech. Brain 129, 1385–98.Google Scholar
Josephs, K A, Knopman, D S, Whitwell, J L, et al. 2005. Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND. Neurology 65, 645–7.Google Scholar
Josephs, K A, Petersen, R C, Knopman, D S, et al. 2006b. Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP. Neurology 66, 41–8.Google Scholar
Josephs, K A, Tang-Wai, D F, Edland, S D, et al. 2004. Correlation between antemortem magnetic resonance imaging findings and pathologically confirmed corticobasal degeneration. Arch Neurol 61, 1881–4.Google Scholar
Josephs, K A, Whitwell, J L, Dickson, D W, et al. 2008a. Voxel-based morphometry in autopsy proven PSP and CBD. Neurobiol Aging 29, 280–9.Google Scholar
Josephs, K A, Whitwell, J L, Duffy, J R, et al. 2008b. Progressive aphasia secondary to Alzheimer disease vs FTLD pathology. Neurology 70, 25–34.Google Scholar
Josephs, K A, Whitwell, J L, Knopman, D S, et al. 2008c. Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype. Neurology 70, 1850–7.Google Scholar
Kandiah, N, Tan, K, Pan, A B, et al. 2008. Creutzfeldt–Jakob disease: Which diffusion-weighted imaging abnormality is associated with periodic EEG complexes? J Neurol 255, 1411–4.Google Scholar
Kartsounis, L D, Crellin, R F, Crewes, H, et al. 1991. Primary progressive non-fluent aphasia: A case study. Cortex 27, 121–9.Google Scholar
Kertesz, A, McMonagle, P, Blair, M, et al. 2005. The evolution and pathology of frontotemporal dementia. Brain 128, 1996–2005.Google Scholar
Kim, E J, Rabinovici, G D, Seeley, W W, et al. 2007. Patterns of MRI atrophy in tau positive and ubiquitin positive frontotemporal lobar degeneration. J Neurol Neurosurg Psychiatry 78, 1375–8.Google Scholar
Kim, Y J, Ichise, M, Erami, S S, et al. 2002. Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP. Mov Disord 17, 303–12.Google Scholar
Kitagaki, H, Hirono, N, Ishii, K, et al. 2000. Corticobasal degeneration: Evaluation of cortical atrophy by means of hemispheric surface display generated with MR images. Radiology 216, 31–8.Google Scholar
Knibb, J A, Xuereb, J H, Patterson, K, et al. 2006. Clinical and pathological characterization of progressive aphasia. Ann Neurol 59, 156–65.Google Scholar
Knopman, D S, Petersen, R C, Edland, S D, et al. 2004. The incidence of frontotemporal lobar degeneration in Rochester, Minnesota, 1990 through 1994. Neurology 62, 506–08.Google Scholar
Kokmen, E, Beard, C M, O'Brien, P C, et al. 1993. Is the incidence of dementing illness changing? A 25-year time trend study in Rochester, Minnesota (1960–1984). Neurology 43, 1887–92.Google Scholar
Kovari, E, Gold, G., Herrmann, F R, et al. 2007. Cortical microinfarcts and demyelination affect cognition in cases at high risk for dementia. Neurology 68, 927–31.Google Scholar
Krause, S, Gohringer, T, Walter, M C, et al. 2007. Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein. Clin Neuropathol 26, 232–40.Google Scholar
Laakso, M P, Partanen, K, Riekkinen, P, et al. 1996. Hippocampal volumes in Alzheimer's disease, Parkinson's disease with and without dementia, and in vascular dementia: An MRI study. Neurology 46, 678–81.Google Scholar
Laureys, S, Salmon, E, Garraux, G, et al. 1999. Fluorodopa uptake and glucose metabolism in early stages of corticobasal degeneration. J Neurol 246, 1151–8.Google Scholar
Ber, I, Camuzat, A, Hannequin, D, et al. 2008. Phenotype variability in progranulin mutation carriers: A clinical, neuropsychological, imaging and genetic study. Brain 131, 732–46.Google Scholar
Ber, I, Martinez, M, Campion, D, et al. 2004. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: Phenotype and suggestive mapping of the DM3 locus to chromosome 15q21–24. Brain 127, 1979–92.Google Scholar
Libon, D J, Price, C C, Giovannetti, T, et al. 2008. Linking MRI hyperintensities with patterns of neuropsychological impairment: Evidence for a threshold effect. Stroke 39, 806–13.Google Scholar
Lippa, C F, Duda, J E, Grossman, M, et al. 2007. DLB and PDD boundary issues: Diagnosis, treatment, molecular pathology, and biomarkers. Neurology 68, 812–9.Google Scholar
Listerud, J, Anderson, C, Moore, P, et al. 2009. Neuropsychological patterns in MRI-defined subgroups of patients with degenerative dementia. J Int Neuropsychol Soc, 15, 459–70.Google Scholar
Litvan, I, Bhatia, K P, Burn, D J, et al. 2003. Movement Disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for Parkinsonian disorders. Mov Disord 18, 467–86.Google Scholar
Lobotesis, K, Fenwick, J D, Phipps, A, et al. 2001. Occipital hypoperfusion on SPECT in dementia with Lewy bodies but not AD. Neurology 56, 643–9.Google Scholar
Lutte, I, Laterre, C, Bodart, J M, et al. 2000. Contribution of PET studies in diagnosis of corticobasal degeneration. Eur Neurol 44, 12–21.Google Scholar
Martindale, J, Geschwind, M D, Armond, S, et al. 2003. Sporadic Creutzfeldt–Jakob disease mimicking variant Creutzfeldt–Jakob disease. Arch Neurol 60, 767–70.Google Scholar
Massimo, L and Grossman, M. 2008. Patient care and management of frontotemporal lobar degeneration. Am J Alzh Dis Other Dementias 23, 125–31.Google Scholar
McKeith, I, O'Brien, J, Walker, Z, et al. 2007. Sensitivity and specificity of dopamine transporter imaging with 123I-FP-CIT SPECT in dementia with Lewy bodies: A phase III, multicentre study. Lancet Neurol 6, 305–13.Google Scholar
McKeith, I G, Dickson, D W, Lowe, J, et al. 2005. Diagnosis and management of dementia with Lewy bodies: Third report of the DLB Consortium. Neurology 65, 1863–72.Google Scholar
McKeith, I G, Galasko, D, Kosaka, K, et al. 1996. Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the consortium on DLB international workshop. Neurology 47, 1113–24.Google Scholar
McKhann, G M, Albert, M S, Grossman, M, et al. 2001. Clinical and pathological diagnosis of frontotemporal dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch Neurol 58, 1803–09.Google Scholar
McMurtray, A M, Chen, A K, Shapira, J S, et al. 2006. Variations in regional SPECT hypoperfusion and clinical features in frontotemporal dementia. Neurology 66, 517–22.Google Scholar
McNeill, R, Sare, G M, Manoharan, M, et al. 2007. Accuracy of single-photon emission computed tomography in differentiating frontotemporal dementia from Alzheimer's disease. J Neurol Neurosurg Psychiatry 78, 350–5.Google Scholar
Meissner, B, Kallenberg, K, Sanchez-Juanc, P, et al. 2008. Isolated cortical signal increase on MR imaging as a frequent lesion pattern in sporadic Creutzfeldt–Jakob disease. Am J Neuroradiol 29, 1519–24.Google Scholar
Mendez, M F, Shapira, J S, McMurtray, A, et al. 2007. Accuracy of the clinical evaluation for frontotemporal dementia. Arch Neurol 64, 830–5.Google Scholar
Mesulam, M, Wicklund, A, Johnson, N, et al. 2008. Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia. Ann Neurol 63, 709–19.Google Scholar
Mielke, M M, Rosenberg, P B, Tschanz, J, et al. 2007. Vascular factors predict rate of progression in Alzheimer disease. Neurology 69, 1850–8.Google Scholar
Minoshima, S, Foster, N L, Sima, A A, et al. 2001. Alzheimer's disease versus dementia with Lewy bodies: Cerebral metabolic distinction with autopsy confirmation. Ann Neurol 50, 358–65.Google Scholar
Minoshima, S, Giordani, B, Berent, S, et al. 1997. Metabolic reduction in the posterior cingulate cortex in very early Alzheimer's disease. Ann Neurol 42, 85–94.Google Scholar
Mori, H, Yagishita, A, Takeda, T, et al. 2007. Symmetric temporal abnormalities on MR imaging in amyotrophic lateral sclerosis with dementia. Am J Neuroradiol 28, 1511–6.Google Scholar
Mosconi, L, Tsui, W H, Herholz, K, et al. 2008. Multicenter standardized 18F-FDG PET diagnosis of mild cognitive impairment, Alzheimer's disease, and other dementias. J Nucl Med 49, 390–8.Google Scholar
Mosimann, U P, Rowan, E N, Partington, C E, et al. 2006. Characteristics of visual hallucinations in Parkinson disease dementia and dementia with Lewy bodies. Am J Geriatr Psychiatry 14, 153–60.Google Scholar
Mukherjee, O, Pastor, P, Cairns, N J, et al. 2006. HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin. Ann Neurol 60, 314–22.Google Scholar
Mummery, C J, Patterson, K, Price, C J, et al. 2000. A voxel-based morphometry study of semantic dementia: Relationship between temporal lobe atrophy and semantic memory. Ann Neurol 47, 36–45.Google Scholar
Mungas, D, Jagust, W J, Reed, B R, et al. 2001. MRI predictors of cognition in subcortical ischemic vascular disease and Alzheimer's disease. Neurology 57, 2229–35.Google Scholar
Murphy, J M, Henry, R G, Langmore, S, et al. 2007. Continuum of frontal lobe impairment in amyotrophic lateral sclerosis. Arch Neurol 64, 530–4.Google Scholar
Murray, R, Neumann, M, Forman, M S, et al. 2007. Cognitive and motor assessment in autopsy-proven corticobasal degeneration. Neurology 68, 1274–83.Google Scholar
Neary, D, Snowden, J S, Gustafson, L, et al. 1998. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 51, 1546–54.Google Scholar
Nestor, P J, Fryer, T D, Hodges, J R, et al. 2006. Declarative memory impairments in Alzheimer's disease and semantic dementia. Neuroimage 30, 1010–20.Google Scholar
Nestor, P J, Graham, N L, Fruer, T D, et al. 2003. Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula. Brain 126, 2406–18.Google Scholar
Neumann, M, Sampathu, D M, Kwong, L K, et al. 2006. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314, 130–3.Google Scholar
Newberg, A B, Mozley, P D, Sadek, A H, et al. 2000. Regional cerebral distribution of [Tc-99m] hexylmethylpropylene amineoxine in patients with progressive aphasia. J Neuroimaging 10, 162–8.Google Scholar
Noe, E, Marder, K, Bell, K L, et al. 2004. Comparison of dementia with Lewy bodies to Alzheimer's disease and Parkinson's disease with dementia. Mov Disord 19, 60–7.Google Scholar
O'Brien, J T, Colloby, S, Fenwick, J, et al. 2004. Dopamine transporter loss visualized with FP-CIT SPECT in the differential diagnosis of dementia with Lewy bodies. Arch Neurol 61, 919–25.Google Scholar
O'Brien, J T, Firbank, M J, Mosimann, U P, et al. 2005. Change in perfusion, hallucinations and fluctuations in consciousness in dementia with Lewy bodies. Psychiatry Res 139, 79–88.Google Scholar
Osaki, Y, Morita, Y, Fukumoto, M, et al. 2005. Three-dimensional stereotactic surface projection SPECT analysis in Parkinson's disease with and without dementia. Mov Disord 20, 999–1005.Google Scholar
Parchi, P, Castellani, R, Capellari, S, et al. 1996. Molecular basis of phenotypic variability in sporadic Creutzfeldt–Jakob disease. Ann Neurol 39, 767–78.Google Scholar
Peigneux, P, Salmon, E, Garraux, G, et al. 2001. Neural and cognitive bases of upper limb apraxia in corticobasal degeneration. Neurology 57, 1259–68.Google Scholar
Phukan, J, Pender, N P, Hardiman, O, et al. 2007. Cognitive impairment in amyotrophic lateral sclerosis. Lancet Neurol 6, 994–1003.Google Scholar
Plotkin, M, Amthauer, H, Klaffke, S, et al. 2005. Combined 123I-FP-CIT and 123I-IBZM SPECT for the diagnosis of parkinsonian syndromes: Study on 72 patients. J Neural Transm 112, 677–92.Google Scholar
Price, C C, Jefferson, A L, Merino, J G, et al. 2005. Subcortical vascular dementia: Integrating neuropsychological and neuroradiologic data. Neurology 65, 376–82.Google Scholar
Price, T R, Manolio, T A, Kronmal, R A, et al. 1997. Silent brain infarction on magnetic resonance imaging and neurological abnormalities in community-dwelling older adults. The Cardiovascular Health Study. CHS Collaborative Research Group. Stroke 28, 1158–64.Google Scholar
Prusiner, S B and Hsiao, K K. 1994. Human prion diseases. Ann Neurol 35, 385–95.Google Scholar
Rabinovici, G D, Furst, A J, O'Neil, J P, et al. 2007. 11C-PIB PET imaging in Alzheimer disease and frontotemporal lobar degeneration. Neurology 68, 1205–12.Google Scholar
Rankin, K P, Rosen, H J, Kramer, J H, et al. 2004. Right and left medial orbitofrontal volumes show an opposite relationship to agreeableness in FTD. Dement Geriatr Cogn Disord 17, 328–32.Google Scholar
Rhee, J, Antiquena, P, Grossman, M, et al. 2001. Verb comprehension in frontotemporal degeneration: The role of grammatical, semantic and executive components. Neurocase 7, 173–84.Google Scholar
Riekkinen, P, Kejonen, K, Laakso, M P, et al. 1998. Hippocampal atrophy is related to impaired memory, but not frontal functions in non-demented Parkinson's disease patients. Neuroreport 9, 1507–11.Google Scholar
Rohrer, J D, Warren, J D, Omar, R, et al. 2008. Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. Arch Neurol 65, 506–13.Google Scholar
Roman, G C, Tatemichi, T K, Erkinjuntti, T, et al. 1993. Vascular dementia: Diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop. Neurology 43, 250–60.Google Scholar
Rosen, H J, Allison, S C, Ogar, J M, et al. 2006. Behavioral features in semantic dementia vs other forms of progressive aphasias. Neurology 67, 1752–6.Google Scholar
Rosen, H J, Gorno-Tempini, M L, Goldman, W P, et al. 2002a. Patterns of brain atrophy in frontotemporal dementia and semantic dementia. Neurology 58, 198–208.Google Scholar
Rosen, H J, Perry, R J, Murphy, J, et al. 2002b. Emotion comprehension in the temporal variant of frontotemporal dementia. Brain 125, 2286–95.Google Scholar
Satoh, K, Shirabe, S, Tsujino, A, et al. 2007. Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt–Jakob disease. Dement Geriatr Cogn Disord 24, 207–12.Google Scholar
Schneider, J A, Boyle, P A, Arvanitakis, Z, et al. 2007. Subcortical infarcts, Alzheimer's disease pathology, and memory function in older persons. Ann Neurol 62, 59–66.Google Scholar
Seeley, W W, Bauer, A M, Miller, B L, et al. 2005. The natural history of temporal variant frontotemporal dementia. Neurology 64, 1384–90.Google Scholar
Skibinski, G, Parkinson, N J, Brown, J M, et al. 2005. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat Genet 37, 806–08.Google Scholar
Snowden, J, Neary, D, Mann, D, et al. 2007. Frontotemporal lobar degeneration: Clinical and pathological relationships. Acta Neuropathol 114, 31–8.Google Scholar
Snowdon, D A, Greiner, L H, Mortimer, J A, et al. 1997. Brain infarction and the clinical expression of Alzheimer disease. The Nun Study. JAMA 277, 813–7.Google Scholar
Soliveri, P, Monza, D, Paridi, D, et al. 1999. Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy. Neurology 53, 502–07.Google Scholar
Swartz, R H, Stuss, D T, Gao, F, et al. 2008. Independent cognitive effects of atrophy and diffuse subcortical and thalamico-cortical cerebrovascular disease in dementia. Stroke 39, 822–30.Google Scholar
Sze, G, Armond, S J, Brandt-Zawadzki, M, et al. 1986. Foci of MRI signal (pseudo lesions) anterior to the frontal horns: Histologic correlations of a normal finding. Am J Roentgenol 147, 331–7.Google Scholar
Talbot, P R, Snowden, J S, Lloyd, J J, et al. 1995. The contribution of single photon emission tomography to the clinical differentiation of degenerative cortical brain disorders. J Neurol 242, 579–86.Google Scholar
Tam, C W, Burton, E J, McKeith, I G, et al. 2005. Temporal lobe atrophy on MRI in Parkinson disease with dementia: A comparison with Alzheimer disease and dementia with Lewy bodies. Neurology 64, 861–5.Google Scholar
Tedeschi, G, Litvan, I, Bonavita, S, et al. 1997. Proton magnetic resonance spectroscopic imaging in progressive supranuclear palsy, Parkinson's disease and corticobasal degeneration. Brain 120, 1541–52.Google Scholar
Turner, R S, Kenyon, L C, Trojanowski, J Q, et al. 1996. Clinical, neuroimaging, and pathologic features of progressive nonfluent aphasia. Ann Neurol 39, 166–73.Google Scholar
Zee, J, Urwin, H, Engelborghs, S, et al. 2008. CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro. Hum Mol Genet 17, 313–22.Google Scholar
Swieten, J and Spillantini, M G. 2007. Hereditary frontotemporal dementia caused by Tau gene mutations. Brain Pathol 17, 63–73.Google Scholar
Vander Borght, T, Minoshima, S, Giordani, B, et al. 1997. Cerebral metabolic differences in Parkinson's and Alzheimer's diseases matched for dementia severity. J Nucl Med 38, 797–802.Google Scholar
Vermeer, S E, Koudstaal, P J, Oudkerk, M, et al. 2002. Prevalence and risk factors of silent brain infarcts in the population-based Rotterdam Scan Study. Stroke 33, 21–5.Google Scholar
Viassolo, V, Previtali, S C, Schiatti, E, et al. 2008. Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: Recurrence of the VCP R155H mutation in an Italian family and implications for genetic counselling. Clin Genet 74, 54–60.Google Scholar
Walker, Z, Costa, D C, Ince, P, et al. 1999. In-vivo demonstration of dopaminergic degeneration in dementia with Lewy bodies. Lancet 354, 646–7.Google Scholar
Walker, Z, Costa, D C, Walker, R W, et al. 2002. Differentiation of dementia with Lewy bodies from Alzheimer's disease using a dopaminergic presynaptic ligand. J Neurol Neurosurg Psychiatry 73, 134–40.Google Scholar
Watts, G D, Thomasova, D, Ramdeen, S K, et al. 2007. Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Clin Genet 72, 420–6.Google Scholar
Whitwell, J L, Jack, C R, Kantacri, K, et al. 2007a. Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations. Arch Neurol 64, 371–6.Google Scholar
Whitwell, J L, Jack, C R, Parisi, J E, et al. 2007b. Rates of cerebral atrophy differ in different degenerative pathologies. Brain 130, 1148–58.Google Scholar
Whitwell, J L, Josephs, K A, Rossor, M N, et al. 2005. Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia. Arch Neurol 62, 1402–08.Google Scholar
Whitwell, J L, Warren, J D, Josephs, K A, et al. 2004. Voxel-based morphometry in tau-positive and tau-negative frontotemporal lobar degenerations. Neurodegener Dis 1, 225–30.Google Scholar
Whitwell, J L, Weigand, S D, Shiung, M M, et al. 2007c. Focal atrophy in dementia with Lewy bodies on MRI: A distinct pattern from Alzheimer's disease. Brain 130, 708–19.Google Scholar
Will, R G, Zeidler, M, Stewart G, E, et al. 2000. Diagnosis of new variant Creutzfeldt–Jakob disease. Ann Neurol 47, 575–82.Google Scholar
Woolley, J D, Gorno-Tempini, M L, Seeley, W W, et al. 2007. Binge eating is associated with right orbitofrontal–insular–striatal atrophy in frontotemporal dementia. Neurology 69, 1424–33.Google Scholar
Yi, H A, Moore, P, Grossman, M, et al. 2007. Reversal of the concreteness effect for verbs in patients with semantic dementia. Neuropsychology 21, 9–19.Google Scholar
Yong, S W, Yoon, J K, An, Y S, et al. 2007. A comparison of cerebral glucose metabolism in Parkinson's disease, Parkinson's disease dementia and dementia with Lewy bodies. Eur J Neurol 14, 1357–62.Google Scholar
Zamboni, G, Huey, E D, Krueger, F, et al. 2008. Apathy and disinhibition in frontotemporal dementia: Insights into their neural correlates. Neurology 71, 736–42.Google Scholar
Zeidler, M, Sellar, R J, Collie, D A, et al. 2000. The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt–Jakob disease. Lancet 355, 1412–8.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×