Associative learning in degenerative neostriatal disorders: Contrasts in explicit and implicit remembering between Parkinson's and huntington's diseases

The performances of 12 patients with Parkinson's disease (PD), 16 with Huntington's disease (HD), and young and old healthy controls were assessed on a number of tests of verbal and nonverbal declarative memory, on a test of nonmotor conditional associative learning (words and colors), and on a number of reaction time (RT) tasks. The RT tasks consisted of cued simple and choice reactions. The relationship between the precue and the imperative stimulus in the S1–S2 paradigm was nonarbitrary in the first series and arbitrary in the second series. The series with arbitrary S1–S2 associations was repeated across two successive blocks of trials. The rationale of the study was to investigate the function of the basal ganglia “complex loop,” and it was postulated that HD patients would show greater deficits because of greater involvement of the caudate nucleus. The patients with HD had the slowest RTs. Across the two blocks with arbitrary S1–S2 associations, the patients with HD but not PD nevertheless showed evidence of learning in their precued RTs. In contrast, the patients with PD were better able to remember the associations in free recall than were the HD patients. It is concluded that patients with PD have relatively greater deficits in procedural learning, whereas those with HD have relatively more impairments in declarative memory, and the greater level of cognitive impairment in HD overall is interpreted as being due to more serious damage to the caudate loop.

[1]  B. Djahanguiri,et al.  The prevention of acute gastric ulcer in the rat by alpha-methyldopa. , 1967, Medicina et pharmacologia experimentalis. International journal of experimental medicine.

[2]  M. Hoehn,et al.  Parkinsonism , 1967, Neurology.

[3]  R W Angel,et al.  Control of movement in Parkinson's disease. , 1970, Brain : a journal of neurology.

[4]  K. Jellinger,et al.  Brain dopamine and the syndromes of Parkinson and Huntington. Clinical, morphological and neurochemical correlations. , 1973, Journal of the neurological sciences.

[5]  K M Heilman,et al.  Reaction times in Parkinson disease. , 1976, Archives of neurology.

[6]  G. Powell,et al.  The relationship between intelligence and verbal and spatial memory. , 1979, Journal of Clinical Psychology.

[7]  S. Fahn,et al.  Huntington disease , 1979, Neurology.

[8]  E V Evarts,et al.  Reaction time in Parkinson's disease. , 1981, Brain : a journal of neurology.

[9]  R. Passingham,et al.  Cortical mechanisms and cues for action. , 1985, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[10]  A. Lang,et al.  Striatal dopamine distribution in Parkinsonian patients during life , 1985, Journal of the Neurological Sciences.

[11]  C. Polkey,et al.  The new Maudsley series of temporal lobectomy. I: Short-term cognitive effects. , 1985, The British journal of clinical psychology.

[12]  R. Passingham,et al.  Premotor cortex and the conditions for movement in monkeys (Macaca fascicularis) , 1985, Behavioural Brain Research.

[13]  C D Marsden,et al.  Visuospatial function in Parkinson's disease. , 1986, Brain : a journal of neurology.

[14]  G. E. Alexander,et al.  Parallel organization of functionally segregated circuits linking basal ganglia and cortex. , 1986, Annual review of neuroscience.

[15]  M. Albert,et al.  Differential patterns of memory loss among patients with Alzheimer's disease, Huntington's disease, and alcoholic Korsakoff's syndrome. , 1986, Archives of neurology.

[16]  H. Freund,et al.  Impairment of rapid movement in Huntington's disease. , 1987, Brain : a journal of neurology.

[17]  R. Taylor Patterns of cognitive impairment in dementia , 1987 .

[18]  T. Robbins,et al.  A comparative study of visuospatial memory and learning in Alzheimer-type dementia and Parkinson's disease. , 1988, Brain : a journal of neurology.

[19]  J. Saint-Cyr,et al.  Procedural learning and neostriatal dysfunction in man. , 1988, Brain : a journal of neurology.

[20]  P. Thompson,et al.  The coexistence of bradykinesia and chorea in Huntington's disease and its implications for theories of basal ganglia control of movement. , 1988, Brain : a journal of neurology.

[21]  S. Kish,et al.  Uneven pattern of dopamine loss in the striatum of patients with idiopathic Parkinson's disease. Pathophysiologic and clinical implications. , 1988, The New England journal of medicine.

[22]  Laura H. Goldstein,et al.  Verbal and Abstract Designs Paired Associate Learning After Unilateral Temporal Lobectomy , 1988, Cortex.

[23]  C. Marsden,et al.  'Frontal' cognitive function in patients with Parkinson's disease 'on' and 'off' levodopa. , 1988, Brain : a journal of neurology.

[24]  B. Rockstroh,et al.  The cerebellum contributes to mental skills. , 1989 .

[25]  D. Salmon,et al.  Neuropsychological evidence for multiple implicit memory systems: a comparison of Alzheimer's, Huntington's, and Parkinson's disease patients , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  R. E. Passingham,et al.  Sequencing ability in Parkinsonians, patients with frontal lobe lesions and patients who have undergone unilateral temporal lobectomies , 1989, Neuropsychologia.

[27]  C. Marsden,et al.  The performance on learning tasks of patients in the early stages of Parkinson's disease , 1989, Neuropsychologia.

[28]  N. Birbaumer,et al.  Slow cortical potentials in Parkinsonian patients during the course of an associative learning task , 1990 .

[29]  C. Marsden,et al.  Prism adaptation and other tasks involving spatial abilities in patients with Parkinson's disease, patients with frontal lobe lesions and patients with unilateral temporal lobectomies , 1990, Neuropsychologia.

[30]  H. Freund,et al.  Premotor cortex and conditional motor learning in man. , 1990, Brain : a journal of neurology.

[31]  E. Marder,et al.  Procedural memory in Parkinson's disease: impaired motor but not visuoperceptual learning. , 1990, Journal of clinical and experimental neuropsychology.

[32]  A. Lees,et al.  Ageing and Parkinson's disease: substantia nigra regional selectivity. , 1991, Brain : a journal of neurology.

[33]  N Quinn,et al.  Reaction times and visuospatial processing in Parkinson's disease. , 1991, Journal of clinical and experimental neuropsychology.

[34]  M. Nissen,et al.  Procedural learning is impaired in Huntington's disease: Evidence from the serial reaction time task , 1991, Neuropsychologia.

[35]  C. Marsden,et al.  PROCEDURAL MEMORY AND NEUROLOGICAL DISEASE , 1992 .

[36]  Bruno Fimm,et al.  Cognitive slowing in decision tasks in early and advanced Parkinson's disease , 1992, Brain and Cognition.

[37]  M. Hallett,et al.  Procedural learning in Parkinson's disease and cerebellar degeneration , 1993, Annals of neurology.

[38]  D. Robinson,et al.  Dopamine dependent reaction time deficits in patients with parkinson's disease are task specific , 1993, Neuropsychologia.

[39]  E. Scholz,et al.  Proximal and distal reaction times (RTs) are not differentially affected in parkinson's disease , 1993, Movement disorders : official journal of the Movement Disorder Society.

[40]  Conditional associative learning is impaired in cerebellar disease in humans. , 1994 .