Associative and recognition memory for novel objects in dementia: implications for diagnosis

It has been demonstrated that patients with dementia of the Alzheimer's type show particular difficulties with a task that measures memory for object locations [R. Swainson et al. (2001) Dement. Geriatr. Cogn. Disord. 12, 265–80]. The present study followed on from this report by asking whether the deficits seen in dementia of the Alzheimer's type were specific to this condition, or whether they would also be seen in another common neurodegenerative syndrome, frontotemporal dementia. To investigate this important issue, we examined memory for object–location pairs and visual recognition memory for novel patterns using two tests, the Paired Associates Learning and Matching to Sample tasks, from the Cambridge Neuropsychological Testing Automated Battery. The performance of a subset of the patients with dementia of the Alzheimer's type described by Swainson et al., selected on the basis of age and education, was compared with matched groups of frontal variant frontotemporal dementia, semantic dementia and control subjects. In contrast to the patients with dementia of the Alzheimer's type, who showed significant impairment on both memory tests, the two frontotemporal dementia groups did not perform significantly poorer compared with control subjects on nearly all memory measures, other than ‘memory score’ from the paired associates learning task. These findings confirm that tests of episodic memory, especially for the location of objects in space, may be useful in the early diagnosis and differentiation of dementia of the Alzheimer's type.

[1]  M. W. Brown,et al.  Episodic memory, amnesia, and the hippocampal–anterior thalamic axis , 1999, Behavioral and Brain Sciences.

[2]  J. Hodges,et al.  Semantic dementia. Progressive fluent aphasia with temporal lobe atrophy. , 1992 .

[3]  Richard S. J. Frackowiak,et al.  Learning to find your way: a role for the human hippocampal formation , 1996, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[4]  M. Mishkin,et al.  Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  Sasha Bozeat,et al.  Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease? , 2000, Journal of neurology, neurosurgery, and psychiatry.

[6]  Endel Tulving,et al.  Organization of memory: Quo vadis? , 1995 .

[7]  J R Hodges,et al.  The prevalence of frontotemporal dementia , 2002, Neurology.

[8]  J R Hodges,et al.  Semantic knowledge and episodic memory for faces in semantic dementia. , 2001, Neuropsychology.

[9]  L. Saksida,et al.  The organization of visual object representations: a connectionist model of effects of lesions in perirhinal cortex , 2002, The European journal of neuroscience.

[10]  E. Rolls,et al.  Selective Perceptual Impairments After Perirhinal Cortex Ablation , 2001, The Journal of Neuroscience.

[11]  B L Miller,et al.  Dietary changes, compulsions and sexual behavior in frontotemporal degeneration. , 1995, Dementia.

[12]  D. C. Howell Statistical Methods for Psychology , 1987 .

[13]  E. Murray,et al.  Monkeys with rhinal cortex damage or neurotoxic hippocampal lesions are impaired on spatial scene learning and object reversals. , 1998, Behavioral neuroscience.

[14]  M N Rossor,et al.  Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease , 2001, Annals of neurology.

[15]  Jordan Grafman,et al.  Associative Learning Impairments in Patients with Frontal Lobe Damage , 1999, Brain and Cognition.

[16]  J. Hodges,et al.  Insights from semantic dementia on the relationship between episodic and semantic memory , 2000, Neuropsychologia.

[17]  E. Murray,et al.  Preserved Recognition Memory for Small Sets, and Impaired Stimulus Identification for Large Sets, Following Rhinal Cortex Ablations in Monkeys , 1994, The European journal of neuroscience.

[18]  L. Saksida,et al.  Perirhinal cortex resolves feature ambiguity in complex visual discriminations , 2002, The European journal of neuroscience.

[19]  D. Gaffan,et al.  The hippocampus, perirhinal cortex and memory in the monkey , 2000 .

[20]  Daniel L. Schacter,et al.  Retrieval without Recollection: An Experimental Analysis of Source Amnesia , 1984 .

[21]  D. Gaffan,et al.  Perirhinal cortex ablation impairs configural learning and paired–associate learning equally , 1998, Neuropsychologia.

[22]  J. Hodges,et al.  Differentiating frontal and temporal variant frontotemporal dementia from Alzheimer’s disease , 2000, Neurology.

[23]  Fergus I M Craik,et al.  Relations between source amnesia and frontal lobe functioning in older adults. , 1990, Psychology and aging.

[24]  S. Gutnikov,et al.  Perceptual and Mnemonic Matching-To-Sample in Humans: Contributions of The Hippocampus, Perirhinal and Other Medial Temporal Lobe Cortices , 2000, Cortex.

[25]  M Mishkin,et al.  Effects of selective neonatal temporal lobe lesions on visual recognition memory in rhesus monkeys , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  E. Tulving Episodic memory and common sense: how far apart? , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[27]  Alan C. Evans,et al.  A cognitive activation study of memory for spatialrelationshipsfn2 fn2 Study conducted at the McConnellBrain Imaging Centre, Montreal Neurological Institute,McGill University. , 1999, Neuropsychologia.

[28]  E. Murray Memory for objects in nonhuman primates , 2000 .

[29]  Leslie G. Ungerleider Two cortical visual systems , 1982 .

[30]  P Alvarez,et al.  Damage limited to the hippocampal region produces long-lasting memory impairment in monkeys , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  B Miller,et al.  The Neuropsychology of Frontal Variant Frontotemporal Dementia and Semantic Dementia. Introduction to the Special Topic Papers: Part II , 2001, Neurocase.

[32]  D. Amaral,et al.  Lesions of the perirhinal and parahippocampal cortices in the monkey produce long-lasting memory impairment in the visual and tactual modalities , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  J. Hodges,et al.  Is semantic memory consistently impaired early in the course of Alzheimer's disease? Neuroanatomical and diagnostic implications , 1995, Neuropsychologia.

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

[35]  D. Amaral,et al.  Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  D. Gaffan,et al.  Impairment of visual object-discrimination learning after perirhinal cortex ablation. , 1997, Behavioral neuroscience.

[37]  J. Bachevalier Medial temporal lobe structures and autism: A review of clinical and experimental findings , 1994, Neuropsychologia.

[38]  P Garrard,et al.  The differentiation of semantic dementia and frontal lobe dementia (temporal and frontal variants of frontotemporal dementia) from early Alzheimer's disease: a comparative neuropsychological study. , 1999, Neuropsychology.

[39]  Alan C. Evans,et al.  Memory for object-features versus memory for object-location: A positron emission tomography study of encoding and retrieval processes , 1996, NeuroImage.

[40]  T. Robbins,et al.  Early Detection and Differential Diagnosis of Alzheimer’s Disease and Depression with Neuropsychological Tasks , 2001, Dementia and Geriatric Cognitive Disorders.

[41]  D. Gaffan,et al.  Learning and transfer of object-reward associations and the role of the perirhinal cortex. , 1998, Behavioral neuroscience.

[42]  L. Squire,et al.  The human perirhinal cortex and recognition memory , 1998, Hippocampus.

[43]  B Miller,et al.  The Classification, Genetics and Neuropathology of Frontotemporal Dementia. Introduction to the Special Topic Papers: Part I , 2001, Neurocase.

[44]  Mieke Verfaellie,et al.  Recollection-based memory in frontotemporal dementia: implications for theories of long-term memory. , 2002, Brain : a journal of neurology.

[45]  T. Bussey,et al.  Perceptual–mnemonic functions of the perirhinal cortex , 1999, Trends in Cognitive Sciences.

[46]  B. Sahakian,et al.  Differing patterns of temporal atrophy in Alzheimer’s disease and semantic dementia , 2001, Neurology.

[47]  J. Semple,et al.  Computerized neuropsychological tests in the early detection of dementia: Prospective findings , 1997, Journal of the International Neuropsychological Society.

[48]  T. Robbins,et al.  Specific cognitive deficits in mild frontal variant frontotemporal dementia. , 1999, Brain : a journal of neurology.

[49]  L. Squire,et al.  Intact visual perceptual discrimination in humans in the absence of perirhinal cortex. , 2000, Learning & memory.

[50]  R. Faber,et al.  Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. , 1999, Neurology.

[51]  J. Becker,et al.  On the relationship between knowledge and memory for pictures: Evidence from the study of patients with semantic dementia and Alzheimer's disease , 1997, Journal of the International Neuropsychological Society.

[52]  M. Mishkin,et al.  Object Recognition and Location Memory in Monkeys with Excitotoxic Lesions of the Amygdala and Hippocampus , 1998, The Journal of Neuroscience.

[53]  John R. Hodges,et al.  The human perirhinal cortex in semantic memory: an in vivo and postmortem volumetric magnetic resonance imaging study in semantic dementia, Alzheimer's disease and matched controls , 2002 .