Object-location memory impairment in patients with thermal lesions to the right or left hippocampus
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
15093141
DOI
10.1016/j.neuropsychologia.2004.01.002
PII: S0028393204000107
Knihovny.cz E-resources
- MeSH
- Brain Damage, Chronic diagnosis physiopathology MeSH
- Dominance, Cerebral physiology MeSH
- Adult MeSH
- Electrocoagulation * MeSH
- Epilepsy, Temporal Lobe surgery MeSH
- Hippocampus physiopathology MeSH
- Memory, Short-Term physiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Brain Mapping MeSH
- Orientation physiology MeSH
- Postoperative Complications diagnosis physiopathology MeSH
- Anterior Temporal Lobectomy * MeSH
- Reference Values MeSH
- Mental Recall physiology MeSH
- Pattern Recognition, Visual physiology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Memory for object-location was investigated by testing subjects with small unilateral thermolesions to the medial temporal lobe using small-scale 2D (Abstract) or large-scale 3D (Real) recall conditions. Four patients with lesions of the left hippocampus (LH), 10 patients with damage to the right hippocampus (RH) and 9 matched normal controls (NC) were tested. Six task levels were presented in a pseudorandom order. During each level, subjects viewed one to six different objects on the floor of a circular curtained arena 2.90 m in diameter for 10 s. Recall was tested by marking the locations of objects on a map of the arena (Abstract recall) and then by replacing the objects in the arena (Real recall). Two component errors were studied by calculating the Location Error (LE), independent of the object identity and the configuration error by finding the best match to the presented configuration. The RH group was impaired relative to the NC for nearly all combinations of recall and error types. An impairment was observed in this group even for one object and it deepened sharply with an increasing object number. Damage to the right perirhinal or parahippocampal cortices did not add to the impairment. Deficits in the LH group were also observed, but less consistently. The data indicate that spatial memory is strongly but not exclusively lateralised to the right medial temporal lobe.
References provided by Crossref.org
Neural correlates of spatial navigation changes in mild cognitive impairment and Alzheimer's disease