Atrophy of Basal Ganglia Nuclei and Negative Symptoms in Temporal Lobe Epilepsy

A consecutive series of 100 patients with temporal lobe epilepsy (TLE) and 92 healthy comparison subjects were available for inclusion in the current study. From this set, 22 patients with negative symptoms (NEG) were matched on age of epilepsy onset to 22 epilepsy patients without negative symptoms (NoNEG) and 22 healthy comparison subjects. Age and gender were also used in matching subjects.

Subjects were recruited from the University of Wisconsin Epilepsy Clinic as part of a larger project examining the neurodevelopmental features of TLE. Individuals were excluded due to mental retardation (IQ<70) or additional neurological diagnoses. Initial selection criteria for the epilepsy patients included a chronological age from 18 to 60 years old and complex partial seizures. Diagnosis was conducted by a board-certified neurologist with expertise in epileptology who reviewed patients’ medical records. This review was blinded to all quantitative imaging data reported here. Healthy comparison subjects were primarily spouses or friends of the TLE participants. Comparison subjects were excluded if they were taking psychotropic medications or if there was evidence of a medical or psychiatric condition or current substance abuse that could affect cognitive functioning. Informed consent was obtained from all participants prior to beginning study procedures.

All participants underwent a comprehensive psychiatric assessment including the Scale for the Assessment of Negative Symptoms (SANS) 24 and the Beck Depression Inventory (BDI). For the SANS, ratings were conducted by three trained investigators for negative symptoms on the SANS. These raters were blinded to information regarding the participants’ cognitive performance or MRI volumes. The SANS contains four global domains including affective flattening or blunting, alogia, avolition-apathy, and anhedonia-asociality. The four domains are made up of 18 individual items. Each subject was rated from absent (0) to severe (5) on each item by three independent raters who then reached a consensus on SANS ratings.

Magnetic resonance images were acquired at the University of Wisconsin-Madison and processed using the semiautomated software package Brain Research: Analysis of Images, Networks, and Systems (BRAINS2). University of Wisconsin staff was blinded to the clinical, sociodemographic, and neuropsychological characteristics of the participants. The T ₁ -weighted images were spatially normalized so that the anterior-posterior axis of the brain was realigned parallel to the anterior commissure-posterior commissure (ACPC) line and the interhemispheric fissure was aligned on the other two axes. A six-point linear transformation was used to warp the standard Talairach atlas space onto the resampled image. Images from the three pulse sequences were then coregistered using a local adaptation of automated image registration software. Following alignment of the image sets, the PD and T ₂ images were resampled into 1 mm cubic voxels following which an automated algorithm classified each voxel into gray matter, white matter, CSF, blood, or “other.” The brains were then removed from the skull using a neural network application that had been trained on a set of manual traces. Manual inspection and correction of the output of the neural network tracing was conducted. A stereotaxic method based on the Talairach atlas yields measures of left and right frontal, temporal, parietal, and occipital lobes and cerebellum. The BRAINS2 software and procedures have been shown to have high interrater and intrarater reliability, and scan-rescan reproducibility. 25

For this investigation, recently developed automated neural networks for the basal ganglia structures, including the caudate, putamen, and globus pallidus, were manually edited based on guidelines published by the University of Iowa Imaging Center. 26 Manual traces of the nucleus accumbens and anterior cingulate were adapted from guidelines available in the scientific literature. 27, 28 All traces were conducted blinded to group membership. Interrater reliability was as follows for the regions of interest: caudate nucleus (0.97), putamen (0.98), globus pallidus (0.94), nucleus accumbens (0.98), and anterior cingulate (0.83). Figure 1 and Figure 2 depict the regions under investigation.

Magnetic resonance imaging volumes were standardized in two ways relative to the value of the total sample of comparison subjects (n=92): using a regression based z-score transformation controlling for the effects of intracranial volume and using a regression based z-score transformation controlling for the effects of height. Beta weights, regression coefficient, and the standard residuals from these analyses were then used to calculate z-scores for the two epilepsy groups (n=44) and the subsample of comparison subjects included in the current study (n=22). Analyses were run using both intracranial volume and height z-score transformations with no difference on the direction of the findings or statistical significance. For the reported analyses, height was chosen as a covariate as it had fewer problems with collinearity with the regions of interest compared to intracranial volume.

The epilepsy patients with negative symptoms (NEG) had an average of 8.8 negative symptoms (SD=6.6, range=1–26) relative to epilepsy patients without negative symptoms (NoNEG) and comparison groups. Affective flattening was the most common negative symptom (59.0%, n=19) followed by alogia (45.5%, n=13), avolition (24.0%, n=7), and anhedonia (18.2%, n=6). The comparison and NEG groups differed on total number of depression symptoms as assessed by the BDI (t=−2.24, df=43, p=0.03, two-tailed). However, there was no significant difference between the two epilepsy groups on BDI score (t=−0.613, df=38, p=0.54) or a significant correlation between number of negative symptoms and total BDI score (r =0.12, p=0.47), or BDI and any of the region of interest volumes examined (p>0.05 in all cases).

Using Wilks’ criterion, a multivariate analysis of variance including all five regions of interest (i.e., average left/right, adjusted for height) yielded a significant difference between groups (F=2.74, df=10, 114, η ² =0.19, p=0.01). Univariate analyses determined that the three groups differed significantly on volumes of the caudate nucleus (F=3.13, df=2, 61, η ² =0.09, p=0.05), the putamen (F=3.69, df=2, 61, η ² =0.11, p=0.03), and the globus pallidus (F=9.65, df=2, 61, η ² =0.24, p=0.001).

Of particular interest are regions in which the NEG TLE group showed significant volume differences from both the comparison and the NoNEG TLE groups, and regions which also showed no differences between the NoNEG and comparison groups. Figure 3 displays these results. Significant differences were found between the healthy comparison and NEG groups for putamen (t=2.43, df=43, η ² =0.12, p=0.02) and the globus pallidus (t=3.59, df=43, η ² =0.23, p=0.001). Critically, the NEG group also had significantly smaller putamen (t=2.21, df=39, η ² =0.11, p=0.03) and globus pallidus (t=3.85, df=39, η ² =0.28, p=0.00) volumes relative to the NoNEG group. There were no significant differences observed between the comparison and NoNEG epilepsy groups on putamen (t=.39, df=40, η ² =0.00, p=0.70) or globus pallidus (t=−0.51, df=40, η ² =0.00, p=0.62). No significant difference was found between the three groups for the volumes of the nucleus accumbens or anterior cingulate. The epilepsy groups did have smaller caudate volumes than the comparison group, but there was no difference between the epilepsy groups on the volumes of the caudate. Moreover, there was no significant difference between the two epilepsy groups on right (t=−1.02, df=35, p=0.34) or left (t=−0.76, df=35, p=0.45) temporal lobe volume or on volumes of the right hippocampus (t=−0.03, df=34, p=0.98) or left hippocampus (t=1.02, df=34, p=0.31). There was no significant relationship between antiepileptic medication and brain volumes.

To further examine the relationship between MRI volumes and negative symptoms, we conducted Pearson’s product-moment correlation coefficients. The negative symptom of alogia was correlated with both the volume of the globus pallidus (r=−0.30, p=0.02) and the putamen (r=−0.29, p=0.02). Affective flattening was significantly correlated with the globus pallidus (r=−0.32, p=0.01). Thus, a higher number of negative symptoms on these dimensions were associated with lower volumes in these regions of interest. There was no relationship between volumes and the negative symptoms of anhedonia-asociality and avolition-apathy.

This is a community based sample of epilepsy patients who were recruited as part of a larger investigation of the neurobehavioral features of TLE. As most of these participants were not surgical candidates and did not undergo video-EEG monitoring, definitive information on the laterality of seizure focus was not available. In that context, we only examined average volume in the basal ganglia areas of interest.

We have speculated on the importance of the amygdala and its interconnectivity with the basal ganglia in the phenomenon of negative symptoms. Amygdalar damage has been observed in TLE. 37 While there is support for this possibility in both animal and human clinical literature, we did not conduct a direct volumetric trace of the amygdala. Future research focusing on the role of the amygdala and negative symptoms in TLE appears warranted.

In our study, we examined volumetric reductions in a sample of TLE patients with and without negative symptoms relative to age- and gender-matched comparison subjects. We found volume reductions in our TLE patients relative to comparison subjects in three out of the five regions of interest. Further, we suggest that the volume reductions in the putamen and globus pallidus observed between the two TLE groups is related to a system-wide disruption associated with negative symptoms. However, future studies should examine these critical areas using other epilepsy groups such as extratemporal or nonfocal generalized epilepsy types. If such groups demonstrate negative symptoms, but not volumetric reductions in the two regions of interest, it would further strengthen our contention that the volume reductions observed in these two regions of interest are specific to negative symptoms in TLE.

In our sample, the epilepsy patients were matched on duration of epilepsy. However, as a cross-sectional study, it is unclear when negative symptoms emerged in the NEG patients. In retrospective studies of schizophrenia patients, negative symptoms have been reported years prior to the onset of the first psychotic episode. 38 Recent attention has been devoted to determining whether the severity of negative symptoms in neuroleptic-naive schizophrenia relates to volumetric changes. In a cross-sectional study involving schizophrenia patients, the volume of the globus pallidus has been shown to be correlated with severity of negative symptoms. 31 In volumetric studies of first episode schizophrenia patients, Glenthoj et al. 15 found evidence of basal ganglia pathology prior to initiating treatment with neuroleptics.