OBJECTIVES Existing speculations regarding the cognitive functions of the right hippocampus suggest a special involvement in non-verbal memory functions. However, all supporting evidence in epileptic patients came from postoperative studies that did not consider the preoperative functioning level. The present study investigates in patients with right temporal lobe epilepsy (RTLE), both preoperatively and postoperatively, the role of the right hippocampus for visual memory, visuoconstruction, and spatial visualisation.
METHODS Two groups of patients with RTLE with and without right hippocampal damage (HC+/n=15 vHC−/n=13) were set up retrospectively thereby taking into account the surgical treatment (selective amygdalohippocampectomyv temporal resections sparing the hippocampus), the postoperative pathological findings (hippocampal sclerosis in the HC+ group) and the seizure outcome (all seizure free). The two groups were compared with regard to their neuropsychological performance preoperatively and 3 months after temporal lobe surgery.
RESULTS The preoperative results indicated impaired visual memory performance only for the HC+patients, whereas the HC− patients exhibited no deficiencies in any of the assessed functions. Postoperatively, both groups exhibited partially improved performances. The type of surgical treatment had no different effects on the postoperative performance changes.
CONCLUSIONS The results suggest that hippocampal damage is the major cause of non-verbal memory deficiencies in preoperative patients with right temporal lobe epilepsy. Hence the results support and extend findings from previous postoperative studies. Right hippocampal resections did not increase the preoperative visual memory deficiencies, thus supporting the view that right temporal lobe resection in general bears only small risks for cognitve deteriorations.
- right temporal lobe epilepsy
- visual memory
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Disorders of material specific learning and memory have long been associated with temporal lobe dysfunctions in focal epilepsy. Whereas the left language dominant temporal lobe is consistently associated with memory impairments for verbal material, the right non-dominant temporal lobe seems important for learning and memory of material that is difficult to verbalise such as unfamiliar faces or visually presented abstract designs (for a review see Milner1). Several studies in resected as well as in non-surgical patients confirm these material specific memory functions of the right temporal lobe.2-5 The deficiencies in visual memory in patients with right temporal lobe epilepsy typically involve learning performance or retention/recognition after a delay whereas short aspects of visual memory, such as immediate recall or memory span, often seem unimpaired.3 6 Cognitive changes after right temporal lobe surgery have not often been documented and determinants of the postoperative cognitive development are not yet clear. In general, right temporal lobe surgery seems to bear only small risks for additional cognitive deficiencies or exaggerations of preoperative impairments7 8; however, there are also studies reporting moderate cognitive declines after surgery.9
Recent research aims to find a functional differentiation within the temporal lobes. For the left temporal lobe there are the first hints that mesial and neocortical temporal structures may subserve different aspects of memory with data acquisitions or working memory being mediated by neocortical temporal structures and long term consolidation and retrieval being mediated by temporomesial structures.10 11 For the right temporal lobe there is some evidence that damage specifically in temporomesial structures may be the cause of impairments in non-verbal memory functions. Milner12 found deficiencies in a visually guided maze learning task after right temporal lobectomy only when the operation included the hippocampal structures. Jones-Gotman et alreported in several studies relations between the severity of memory impairments and the extent of hippocampal, but not of neocortical, excisions in the right temporal lobe.13-15 However, all this evidence came from postoperative studies and did not consider the preoperative functioning level.
The goal of the present study was to evaluate the hippocampal contribution to visual memory by comparing neuropsychological performances of patients with RTLE (right temporal lobe epilepsy) with and without hippocampal damage preoperatively and postoperatively. In particular, we checked the questions, whether already preoperatively a prominent association of non-verbal memory deficiencies with hippocampal damage can be found and whether right temporal lobe resections including or not including the hippocampus differentially affect the cognitive outcome. A functional differentiation of various structures within the right temporal lobe could improve the preoperative neuropsychological localisational diagnostics and could help to make predictions of the postoperative cognitive outcome in individual patients.
Two groups of patients with RTLE were retrospectively set up: one group with damage restricted to the hippocampal structure (HC+ group) and the other group with damage not involving the hippocampal structure (HC- group). Selection criteria for the HC+ group were: selective amgydala-hippocampectomy as the surgical treatment, evidence of an ammons horn sclerosis in the histopathological finding, seizure free after surgery. Selection criteria for the HC- group were: no evidence of an ammons horn sclerosis or atrophy in the preoperative high resolution MRI, surgical treatment completely spared the hippocampal structure, seizure free after surgery. Because the most temporal lobe resections include the hippocampus, we found on the whole only 13 patients in our clinical population who fulfilled the HC-criteria, but 47 patients who fulfilled the HC+ criteria. To optimise the conditions for the statistical analyses we equalised the sample sizes by selecting out of the 47 HC+ patients a group of 15 patients who largely matched the HC− patients with respect to the age at surgery, the onset of epilepsy, and the sex ratio.
Surgical treatment in the HC− patients consisted of nine lesionectomies (+1 cm margins), three lobectomies, and one tailored resection. Specific sites of resections varied widely. Pathological findings in the HC− patients were “benign tumours” in 10 patients, “malign tumour” (astrocytoma WHO II) in one patient, and “other lesions” in two patients.
Surgical procedures had been preoperatively dictated by MRI findings and electrophysiological interictal and ictal recordings with surface and sphenoidal electrodes in all patients and intracranial recordings in nine patients (depth electrodes+subdural strips in seven patients, subdural strips in two patients).
Groups did not differ in clinical characteristics (table 1). Preoperative global intellectual functioning, estimated by a vocabulary test,16 as well as preoperative and postoperative psychomotor speed, assessed with a letter cancellation test,17 were average in both groups and there were no significant group differences. Hand dominance assessed with the Oldfield inventory18 indicated non-right hand dominance in six patients. These patients underwent preoperative intracarotid amytal tests, which indicated left hemispheric language dominance despite the atypical hand dominance.
We evaluated visual memory using a task which has already been proved to be sensitive to right temporal dysfunctions.19Furthermore, we assessed visuospatial and visuoconstructional performances as right hemispheric cognitive functions, which are assumed not to specifically tap the temporal lobe.
Visual memory was assessed by the DCS-R, a revised version of the DCS20 (for detailed description see Helmstaedter et al 19 21). A parallel form was used in the postoperative examination. The DCS-R requires repeated learning of nine abstract designs (figure A) in six consecutive trials. The designs are presented consecutively on separate cards at a rate of 2 seconds per item. After each presentation the patient has to reconstruct as many items as possible using five wooden sticks of equal length. Patients are instructed to keep the design and the spatial arrangement identical with the target item. If the reproduction of the design is correct but its spatial positioning is mirrored or at least 30° rotated, it is scored as a “rotation”. If the reproduction of the design is incorrect, it is scored as a “false positive”. After 30 minutes of a verbal distractor task, recognition of the original figures out of 21 distractors (nine rotated original designs and 12 similar designs) is required.
The evaluated indices were learning capacity (sum of correct reproductions in trials 1 to 6), rotations (sum of rotated designs in trials 1 to 6), failures (sum of false positives in trials 1 to 6), and recognition (correctly recognised items−falsely recognised distractors).
Visuoconstructive abilities were assessed using a German adaptation of the block design subtest of the WAIS.22 The evaluated variable was the age related total T value.
Spatial visualisation was assessed using subtest 8 of the Leistungs-Prüf system.23 It requires matching of indicated positions in two dimensionally and three dimensionally drawn figures (figure B). The evaluated variable was the age related c value.
To illustrate results in comparison with healthy subjects and to facilitate the comparison of the different test performances, all results were uniformly transformed into standardised values (mean 100 (SD 10)) (for formula see f.i. in chapter 12, Lienert24). Visual memory variables were standardised using values of a sample of 102 healthy controls (mean (SD) learning capacity 34.7 (9.6); rotations 2.4 (3.4); failures 6 (5.1); recognition 7 (1.9)) who corresponded to the patient groups for age (mean 29.8 (SD 8.8)) years and sex ratio (50 males, 52 females). For the the block design test and the spatial visualisation task age related T and c values, provided in the test manuals, were transformed into standardised scores using the formulas: standard score=100+10((T-50):10) and standard score=100+10((c-5):2).24
Firstly, results are described in comparison with healthy controls. Secondly, preoperative group differences are evaluated by means of a multivariate analysis of variance (MANOVA) and subsequent unvariate analyses of variance (ANOVAs). Thirdly, postoperative data are evaluated with respect to the significance of performance changes (paired t tests) and to significant group differences in the postoperative development (analyses of covariance incorporating the preoperative scores as covariates (ANCOVAs))
The statistical analyses were performed using the statistical package SPSS 6.0 for Windows.
COMPARISON WITH HEALTHY CONTROLS
Preoperative and postoperative results are listed in table 2. The representation in standardised scores allows a comparison with the performance of healthy controls. The HC+ patients scored preoperatively below average (standardised scores<90) in all variables of the visual memory task with learning capacity being the prominent impairment. Postoperatively, they showed impaired performance only in two indices of visual memory (learning capacity, recognition). Mean performances of the HC− patients were preoperatively and postoperatively completely within the normal range (mean ± 1 SD).
Preoperative group differences were first evaluated by a multivariate analysis, as the visual memory indices, except the rotational errors, were significantly correlated (Pearson correlations: r between 0.4 and 0.76 with p<0.05). The MANOVA with surgical treatment (HC+/HC−) as the group factor and the neuropsychological indices as dependent variables yielded a significant overall group effect (Hotellings T=0.85, exact F=3.4, p=0.002), thus indicating that there were overall differences in the preoperative performance of the HC+ and the HC− patients. To check separately which tests yielded the overall group difference, separate univariate ANOVAs with surgical treatment as the group factor were performed on the neuropsychological indices. These indicated significantly lower performances of the HC+ group in all assessed indices (learning capacity: F=17.8, p<0.01; recognition:F=4.5, p=0.045; rotations: F=9.8, p=0.04; failures: F=12.6, p=0.001; spatial visualisation:F=6.5, p=0.02; visuoconstruction: F=11.6, p=0.002).
It has to be considered that our visual memory task also poses high constructional demands. To investigate, therefore, to what extent the group differences in memory could be accounted for by the group differences in visuoconstruction, we computed separate ANCOVAs with the visual memory indices as dependent variables including visuoconstruction as a covariate. Group differences in visual memory largely remained, but significances became slightly less impressive (learning capacity: F=5.4, p=0.03, rotations:F=11.7, p=0.002, failures: F=5.5,P=0.03).
To evaluate the effects of the surgical treatment, ANCOVAs with surgical treatment as the group factor were computed for the pre−post difference scores (preoperative score−postoperative score) incorporating the preoperative scores as covariates. Inclusion of the preoperative values was necessary, as it has often been shown that the preoperative performance level influences the postoperative change.25 There were no significant group differences (F between 0.04 and 2.6 with p between 0.9 and 0.12) thus indicating that the kind of surgical treatment had no different effects on the postoperative development.
To evaluate whether there were any significant postoperative performance changes we computed paired t tests for the total group. These indicated significant postoperative gains for rotations in visual memory (t=−2.5, p=0.18) and for the visuoconstructional abilities (t=−5.7, p<0.001).
This study assessed right hemispheric cognitive functions in patients with right hippocampal sclerosis who had selective amygdalohippocampectomy (HC+) and in patients who received right temporal lobe resections which spared the hippocampal tissue (HC−). Neuropsychological examinations were done preoperatively and 3 months after surgery.
Preoperative results indicated visual memory deficiencies only for the patients with hippocampal sclerosis. These patients scored significantly worse in the visual memory task than patients with extrahippocampal pathology and their performance was below average compared with healthy controls. The deficits in visual memory could not be attributed to impaired visuoconstructive abilities. The HC− patients, on the other hand, showed no deficit in any assessed function. The different preoperative performance patterns of HC+ and HC− patients suggest that, within the right temporal lobe, the hippocampus is critically involved in non-verbal memory functions. Hence the results support and extend the findings of studies that have found the same relation in postoperative patients.12-15 Visual memory performance could therefore be used in the preoperative neuropsychological examination to determine the functional integrity of the hippocampal structure. An explanation is needed for the total lack of deficiencies in the HC−group. It may be that the applied tests do not assess right temporal cognitive functions beyond the hippocampal functions. Another explanation could be that deficiencies are blurred by the variability of lesion sites in these patients with extrahippocampal lesions.
Regarding postoperative development, the type of surgical treatment had no different effects on the assessed neuropsychological performances. No significant deteriorations were evident for either group, thus supporting the general view that right temporal lobe surgery bears only small risks for additional cognitive deficiencies or exaggerations of preoperative impairments. Significant gains were postoperatively evident for rotational errors in the visual memory task and for visuoconstructive abilities. Because all patients in our sample were seizure free after surgery, these gains could be interpreted as a release effect of right hemispheric functions beyond the resection site. If we assume a special contribution of the right hippocampus to non-verbal memory, it is rather surprising that excisions of the hippocampus did not exaggerate the preoperative deficiencies, but that the HC+ patients even slightly improved in visual memory. Rausch26 suggested that the often reported lack of increased deficiencies after a right temporal lobe resection may indicate a comparably large functional plasticity of the right temporal lobe. In this respect, an epileptic hippocampus may be worse than no hippocampus for intrahemispheric or interhemispheric reorganisation.
In conclusion, in line with previous postoperative studies our results verify a special involvement of the right hippocampus in learning and memory for non-verbal material. Patients with hippocampal damage showed preoperatively and postoperatively impaired visual memory performance whereas patients without hippocampal damage exhibited no deficiencies in visual memory. Visual memory deficiencies were not exaggerated after right hippocampal resections. Rather, postoperative data indicated improvements which could be interpreted as release effects and supported the notion that right temporal lobe resections bear only small risks for cognitive deteriorations.
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