 |
 |

Neuropsychological Changes in Olivopontocerebellar Atrophy
Stanley Berent, PhD;
Bruno Giordani, PhD;
Sid Gilman, MD;
Larry Junck, MD;
Shirley Lehtinen, MA;
Dorene S. Markel, MS;
Michael Boivin, PhD;
Karen J. Kluin, MS;
Randolph Parks, PhD;
Robert A. Koeppe, PhD
Arch Neurol. 1990;47(9):997-1001.
Abstract
 |  |
We used standardized neuropsychological measures of intellectual, cognitive, psychomotor, and emotional functioning to compare 39 patients with olivopontocerebellar atrophy and 25 normal controls of similar age. The patients reflected greater depression, anxiety, and subjective emotional discomfort than did the control subjects. While 4 of the patients had below-normal IQ scores (Wechsler Adult Intelligence Scale [WAIS-R] Full-Scale IQ [FSIQ] <80), their clinical histories suggested lifelong functioning at such levels. As a group, the patients were not abnormal in general intellectual functioning and related cognitive abilities (WAIS-R FSIQ, mean [±SD], 93.46 ± 13.19; Wechsler Memory Scale mental quotient, 108.95 ± 17.43). These scores were lower than those of the normal controls (WAIS-R FSIQ, 113.72 ± 12.68; mental quotient, 127.80 ± 12.40); however, the controls were a highly educated group with intelligence levels that were higher than those of the average population. Moreover, when education and motor dysfunction were statistically covaried, no significant differences between the patients and the normal controls were apparent on the cognitive and intellectual tasks. Further analysis of specific memory performance in a subgroup of patients and controls matched for age, sex, and education yielded findings that were comparable with the overall group analysis. We conclude that motor dysfunction and depressed mood could leave patients with olivopontocerebellar atrophy appearing to be impaired in memory, even demented, when they are not.
Author Affiliations
From the Departments of Psychiatry (Drs Berent, Giordani, Boivin, and Parks and Ms Lehtinen), Neurology (Drs Berent, Gilman, and Junck and Ms Markel), Psychology (Drs Berent and Giordani), Nuclear Medicine (Dr Koeppe), and Physical Medicine and Rehabilitation (Ms Kluin), University of Michigan, Ann Arbor.
Footnotes
Accepted for publication November 29, 1989.
Reprint requests to Neuropsychology Program, 480 Med Inn, Box 0840, University of Michigan Hospitals, 1500 E Medical Center Dr, Ann Arbor, MI 48109-0840 (Dr Berent).
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Evaluating the Affective Component of the Cerebellar Cognitive Affective Syndrome
Wolf et al.
J. Neuropsychiatry Clin. Neurosi. 2009;21:245-253.
ABSTRACT
| FULL TEXT
Cognitive Impairments in Cerebellar Degeneration: A Comparison With Huntington's Disease
Brandt et al.
J. Neuropsychiatry Clin. Neurosi. 2004;16:176-184.
ABSTRACT
| FULL TEXT
Phonological grouping is specifically affected in cerebellar patients: a verbal fluency study
Leggio et al.
J. Neurol. Neurosurg. Psychiatry 2000;69:102-106.
ABSTRACT
| FULL TEXT
Trinucleotide Repeat Expansion and Neuropsychiatric Disease
Margolis et al.
Arch Gen Psychiatry 1999;56:1019-1031.
ABSTRACT
| FULL TEXT
Focusing Attention on Cognitive Impairment in Spinocerebellar Ataxia
Geschwind
Arch Neurol 1999;56:20-22.
FULL TEXT
Preserved performance by cerebellar patients on tests of word generation, discrimination learning, and attention.
Helmuth et al.
Learn. Mem. 1997;3:456-474.
ABSTRACT
Psychological Factors and Pet Measured Glucose Metabolism in Olivopontocerebellar Atrophy
Berent et al.
Assessment 1996;3:339-349.
ABSTRACT
Methodologic Considerations in Neuropsychologic Testing of Ataxic Patients
Lalonde et al.
Arch Neurol 1992;49:218-218.
ABSTRACT
Methodologic Considerations in Neuropsychologic Testing of Ataxic Patients-Reply
Berent et al.
Arch Neurol 1992;49:218-219.
ABSTRACT
|