Neuropsychiatric features of corticobasal degeneration
- aNeuropharmacology Unit, Defense and Veteran Head Injury Program, Jackson Foundation and the Medical Neurology Branch, bNational Institutes of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA, cDepartment of Neurology, dDepartment of Psychiatry and Biobehavioral Science, UCLA School of Medicine, Los Angeles, CA, USA
- Dr Irene Litvan, NINDS, NIH, Federal Building, Room 714, Bethesda, MD 20892–9130, USA. Telephone 001 301 496 1189; fax 001 301 496 2358.
- Received 2 February 1998
- Revised 27 April 1998
- Accepted 7 May 1998
OBJECTIVE To characterise the neuropsychiatric symptoms of patients with corticobasal degeneration (CBD).
METHODS The neuropsychiatric inventory (NPI), a tool with established validity and reliability, was administered to 15 patients with CBD (mean (SEM), age 67.9 (2) years); 34 patients with progressive supranuclear palsy (PSP) (66.6 (1.2) years); and 25 controls (70 (0.8) years), matched for age and education. Both patient groups had similar duration of symptoms and mini mental state examination scores. Semantic fluency and motor impairment were also assessed.
RESULTS Patients with CBD exhibited depression (73%), apathy (40%), irritability (20%), and agitation (20%) but less often had anxiety, disinhibition, delusions, or aberrant motor behaviour (for example, pacing). The depression and irritability of patients with CBD were more frequent and severe than those of patients with PSP. Conversely, patients with PSP exhibited significantly more apathy than patients with CBD. The presence of high depression and irritability and low apathy scale scores correctly differentiated the patients with CBD 88% of the time. The irritability of patients with CBD was significantly associated with disinhibition (r=0.85) and apathy (r=0.72). In CBD, apathy was associated with disinhibition (r=0.67); disinhibition was associated with aberrant motor behaviour (r=0.68) and apathy (r=0.67); and aberrant motor behaviour with delusions (r=1.0). On the other hand, depression was not associated with any other behaviour, suggesting that it has a different pathophysiological mechanism. Symptom duration was associated with total motor scores (r=0.69). However, total motor score was not associated with any behaviour or cognitive scores.
CONCLUSIONS The findings indicate that frontosubcortical pathways mediating cognition, emotion, and motor function in CBD are not affected in parallel. Patients with CBD and PSP have overlapping neuropsychiatric manifestations, but they express distinctive symptom profiles. Evaluating the behavioural abnormalities of parkinsonian patients may help clarify the role of the basal ganglia in behaviour.
Corticobasal degeneration (CBD) is a neurodegenerative disorder characterised clinically by steadily progressive motor (for example, dystonia, asymmetric parkinsonism not benefitting from levodopa therapy, myoclonus, balance disturbances, and pyramidal signs) and cognitive (for example, ideomotor apraxia, alien hand syndrome, aphasia, visual and sensory neglect) disturbances presenting after the age of 40.1 2 Neuropathologically, it features circumscribed parietal or frontoparietal atrophy, severe cortical neuronal loss, and intense astrogliosis, spongiosis, swollen and achromatic neurons (ballooned cells), neuropil threads, and occasionally, neurofibrillary tangles. In addition, basophilic argyrophilic and tau protein positive inclusions are found in the neurons of the substantia nigra and basal ganglia (subthalamic nucleus, striatum, and pallidum), and also may be present along the dentatorubrothalamic tracts. Feany and Dickson3 recently described the “astrocytic plaque” as being pathognomonic of this disorder. Clinical and neuropathological variations have been described which overlap with progressive supranuclear palsy (PSP) and Pick’s disease.1 2 4-9 Several studies have characterised the motor and cognitive features of CBD,1 10-14 but the patients’ neuropsychiatric symptoms have rarely been described.15 16
Neuropsychiatric symptoms are important predictors of burden of the caregiver and the potential for admitting patients to institutions.17-20 Thus identification and treatment of the associated behavioural abnormalities may be relevant for improving the quality of life of patients with CBD and their caregivers. In addition, increasing insight into the neurobiological basis of neuropsychiatric disorders facilitates understanding how behaviourally relevant circuits are involved in CBD.
We administered the neuropsychiatric inventory (NPI), a tool with established validity and reliability, to assess the behavioural abnormalities of patients with CBD.21 The NPI evaluates both the frequency and severity of 10 behaviours that are commonly reported in patients with cognitive disturbances: delusions, hallucinations, agitation, depression, anxiety, euphoria, apathy, disinhibition, irritability, and aberrant motor behaviour (for example, pacing). To better characterise the behavioural aspects of patients with CBD and to search for distinctive behavioural characteristics, we compared their performance on the NPI to that of a group of patients with PSP of similar age, education, and cognitive impairment and to age matched normal controls.
Subjects and methods
Fifteen patients with CBD and 34 with PSP, presenting to the National Institutes of Neurological Disorders and Stroke (NINDS) as outpatients, participated in the study (table 1). The patients with CBD were diagnosed according to the modified criteria of Lang et al.4 which included a progressive course of an asymmetric parkinsonism not benefiting from levodopa therapy; the presence of either a dystonic limb or focal myoclonus; the presence of either ideomotor apraxia, alien limb syndrome, or cortical sensory loss; and absence of resting tremor, autonomic disturbance, or laboratory evidence of other disorders. The diagnosis of one of the 15 patients with CBD was later confirmed by necropsy. The PSP study subjects met the NINDS-Society for PSP, Inc (NINDS-PSP) clinical research criteria and 22 have previously been reported on.22
Twenty five normal controls of the same age and educational levels were recruited at the University of California, Los Angeles (table1).21 Exclusion criteria for all subjects and patients comprised history of alcohol or substance misuse, head trauma with loss of consciousness, and psychiatric disorder preceding the onset of current disease. All participating subjects gave institutional consent. Caregivers and participating subjects were interviewed with the NPI, but as previously described,21 the NPI is based on caregivers’ information. Briefly, screening questions for each behaviour were posed first, and if a positive response was obtained for one of the 10 neuropsychiatric domains, then this aspect was further explored with scripted questions. The behaviours were rated using a scale for the frequency (1 being occasionally, 2 often, 3 frequently, and 4 very frequently) and for the severity (1 being mild, 2 moderate, and 3 marked). The composite score for each behavioural domain is the product of the frequency and severity subscore for that particular behaviour (maximum 12). The total score of the NPI is the sum of the subscales scores. In addition, we administered the mini mental state examination (MSSE)23 to all subjects, and the Mattis dementia rating scale24 to 12 of the 15 patients with CBD and to 28 of 34 with PSP. There were no significant differences between patients that were administered the Mattis dementia rating scale and those that were not, (age, education, MMSE scores, symptom duration, and motor scores). Verbal fluency (semantic fluency: number of names of items from a supermarket and phonemic fluency: number of words starting with the letter “F”, produced in one minute), and motor impairment (modified unified Parkinson’s disease rating scale total motor score (UPDRS)25) were assessed in the patients. We computed the motor function axially and in the most affected limb. Both patient groups had similar symptom duration, MMSE, and Mattis dementia rating scale scores, but the patients with CBD had a higher UPDRS total motor score (table 1).
Statistical analyses included bootstrap analysis, analysis of variance (ANOVA), logistic regression, and discriminant function analyses. A histogram of NPI data disclosed that composite scores do not generate a normal distribution. Multiplying the frequency (1–4) by the severity (1–3) subscores will not produce a 5, 7, or 11 composite score. The use of non- parametric analysis (for example, the Mann-WhitneyU test) partially accommodates such skewed data but results in a loss of power. Because NPI data generate a non-normal distribution, precluding traditional parametric analysis, a bootstrap analysis26 was employed. The program Resampling Stats® was used to evaluate significant differences among patient groups’ mean composite scores for each of the 10 NPI behaviours. Bootstrap analysis combines the raw composite scores for any given behaviour of the entire dataset and randomly samples a number of these scores equal to the number making up the groups comprising the data set. A mean difference composite score is then calculated from the randomly comprised samples. This is then repeated 1000 times on the dataset, producing a distribution of possible mean difference composite scores. The mean differences found can then be compared to this distribution of the possible mean difference composite scores between two clinical groups for each behaviour on the NPI. The probability of finding the observed mean difference based on the mean difference generated by resampling is then recorded. This process was repeated 10 times for each of the 10 NPI behaviours to arrive at an average probability value for each comparison. If the observed difference was greater than 95% of the differences expected from random resampling in the bootstrap method, it was judged to be significant at the 0.05 level.
To explore the relations among the different behaviours, symptom duration, and motor and overall cognitive functions, Spearman correlation coefficients were calculated for the composite scores of these, in a 14×14 matrix for all patients with CBD (table 2). This exploratory analysis was not meant to establish strict significance, and thus a type 1 error was deemed preferable to missing a possible correlation (type 2 error). For this reason, no Bonferroni adjustment was made; however, an adjusted α level of 0.01 was required for significance.
Patients with CBD exhibited depression (73%), apathy (40%), irritability (20%) and agitation (20%), but rarely (⩽14%) anxiety, disinhibition, delusions, or aberrant motor behaviour (table 3). No patient with CBD manifested euphoria or hallucinations.
The depression and irritability of patients with CBD were significantly more frequent and severe than those of patients with PSP and normal controls. However, those with PSP exhibited significantly more apathy. The other behaviours were similar in the two patient groups (table 3).
Logistic regression analysis indicated a significantly higher frequency of depression (χ2=13, p<0.001, odds ratio=1299) and irritability (χ2=15.4, p<0.001; odds ratio=27 065) and lower apathy (χ2=22; p<0.0001; odds ratio=0.0001) in patients with CBD compared with patients with PSP (overall model, 39.4; p<0.0001). A discriminant function analysis performed on the patient data set (CBD and PSP) disclosed that any patient with high depression and irritability scale scores and low apathy composite scores would be placed correctly in the CBD group 88% of the time in this patient sample (sensitivity 67%, specificity 97%, overall accuracy 88%).
The irritability of patients with CBD was significantly associated with disinhibition and apathy (table 2). Their apathy was associated with disinhibition and anxiety; their disinhibition was associated with aberrant motor behaviour and delusions; their delusions were associated with aberrant motor behaviour; and their anxiety was associated with delusions and aberrant motor behaviour. Although motor disturbances were not associated with any behaviour, they were associated with total MMSE, suggesting that some patients with CBD with the poorest motor function (higher scores) had better cognitive performance (higher total MMSE scores). A factor analysis was performed to investigate whether the strength of some correlations (for example, disinhibition, anxiety, apathy, irritability, aberrant motor behaviour) may suggest that these behaviours belong to a single syndrome rather than being independent behavioural domains. The analysis showed that these behaviours could be grouped into two factors: (1) irritability, disinhibition, and apathy and (2) anxiety and aberrant motor behaviour (p<0.0001). When we also included agitation and depression in the analysis, these behaviours were grouped into two factors: (1) agitation, apathy, disinhibition, irritability, and aberrant motor behaviour and (2) depression (p<0.0001). Anxiety was included with both but more with factor 1.
Patients with CBD with left motor symptoms (n=7) had higher disinhibition (2 (SEM 1)), apathy (2.8 (SEM 2)) and irritability (2 (SEM 1)), and lower depression scores (2.4 (SEM 1)) than those with right motor symptoms (n=8; disinhibition, 0; apathy, 0.7 (SEM 0.6); irritability, 0.14 (SEM 0.1); depression, 4.6 (SEM 1.4), but none of these differences were significant.
This is the first study to systematically investigate the neuropsychiatric disturbances of patients with CBD. We found that most (87%) patients with CBD manifested neuropsychiatric symptoms, mostly depression (73%), apathy (40%), irritability (20%), and agitation (20%), and less commonly, anxiety, disinhibition, aberrant motor behaviours, or delusions. No patients evidenced euphoria or hallucinations as reported by caregivers on the NPI. Patients with CBD showed significantly more depression than both patients with PSP and controls; conversely, patients with PSP were more apathetic. Behaviouraly, patients with CBD were more likely (higher odds ratios) than those with PSP to exhibit depression and irritability in the absence of, or with low levels of, apathy. In fact, these features correctly identified the patients with CBD 88% of the time. However, patients with CBD also exhibited apathy which was unrelated to their depression. Apathy was manifested by inattention to usual interests, activities, or plans of family members, and by being less spontaneous and active than usual. Apathy of patients with CBD was associated with irritability, disinhibition, and anxiety suggesting possible common pathogenetic mechanisms. Irritability of patients with CBD was manifested by flashes of anger, impatience, being argumentative and difficult to get along with, unrelated to the frustration of their illness, and different from the patient’s usual behaviour. Disinhibition was characterised by acting impulsively without considering the consequences and by being tactless or making crude remarks. Although, it could be argued that the combination of these features is counterintuitive, a factor analysis suggested that irritability, disinhibition, and apathy may belong to a single syndrome rather than being independent behavioural domains. This factor contains items indicative of frontal lobe dysfunction. In support of our findings, a recent study confirmed by necropsy showed that 58% of the patients with CBD studied had developed apathy, irritability, or disinhibition, often associated with frontal lobe release signs.16
In the current study, depression was the most frequent neuropsychiatric symptom exhibited by patients with CBD. These results differ from those of our necropsy study in which only a few (7%) patients with CBD presented with depression at onset, although at least one third developed it during progression of disease.16Neuropsychiatric symptoms are usually not thoroughly ascertained, and necropsy studies probably underestimate their presence. We did not determine if our patients’ depression was reactive to their deficits, but the fact that it may antedate motor symptomatology (and was the first symptom in one of the 15 patients) indicates that at least in some patients with CBD, depression has a neurobiological basis. Depression in CBD was unrelated to any other behaviour, suggesting that its pathophysiological mechanism differed. Depression often occurs in other basal ganglia disorders such as Parkinson’s disease and Huntington’s disease, in which it may predate other symptoms.27-32 Depressed patients with Parkinson’s disease have more severe neuronal loss in the dorsal raphe than non-depressed patients33; and in an18F-fluoro-2-deoxyglucose (18F-FDG) PET study, there was significant hypometabolism in the caudate and orbital inferior frontal lobes.34 In addition, the depression scores of the patients with Parkinson’s disease inversely correlated with the decreased metabolic activity (lower metabolism correlated with greater depression).34 Similarly, in an18F-FDG PET study, depressed patients with Huntington’s disease showed orbitofrontal and thalamic hypometabolism.35 Studies with 18F-FDG PET in CBD disclose diminished metabolic activities in the frontal, temporal, sensorimotor, and parietal association cortices as well as in the caudate nucleus, lenticular nucleus, and thalamus.36 37Studies with PET of regional oxygen uptake show significantly depressed values in the superior and posterior temporal, inferior parietal, and occipital cortices. In addition, there were significant abnormalities in the superior frontal, midfrontal, inferior frontal, frontal polar, and orbitofrontal areas of the prefrontal cortex.38Striatal fluorodopa uptake measured with PET discloses diminished fluorodopa uptake in both the caudate and putamen. These metabolic abnormalities tend to be asymmetric with greater involvement contralateral to the most affected side of the body. The regions affected are similar to those described as abnormal in patients with other neurologically based depression syndromes, although no specific metabolic studies of patients with CBD with and without depression have been reported. Pathological changes in CBD include involvement of several nuclei of frontosubcortical circuits posited to mediate cognitive and emotional functions. Affected areas include the prefrontal cortex, globus pallidus, subthalamic nucleus, substantia nigra, locus coeruleus, raphe nuclei, and midbrain tegmentum.39 Biochemical deficits in CBD include a marked loss of noradrenaline and serotonin as well as a severe nigrostriatal dopamine deficiency.40 Similar transmitter deficiencies characterise other basal ganglia disorders with depression such as Parkinson’s disease. By contrast, in PSP the locus coeruleus and raphe nuclei are relatively preserved, and noradrenaline and serotonin concentrations are usually not affected. Additionally, in PSP, by contrast to what occurs in CBD and Parkinson’s disease, involvement of the frontosubcortical circuits is bilateral and symmetric. Whether unilateral or asymmetric involvement of the orbitofrontal circuit is needed to manifest biological depression, and bilateral involvement of the medial frontal circuits is necessary for the presence of apathy, need further evaluation.
Dysfunction of subcortical projections to premotor-motor and supplementary motor subcortical circuits explains the motor abnormalities exhibited by patients with CBD. Although in our study, patients’ symptom duration was associated with disinhibition (r=0.53) and motor scores (r=0.53), motor disturbances were unrelated to any behaviour or specific cognitive disturbance (for example, frontal dysfunction). Moreover, patients with CBD with worse motor dysfunction (higher scores) had less cognitive impairment (higher total MMSE scores), suggesting that the various frontosubcortical pathways in CBD are not affected in parallel, at relatively early stages of the disease. Because this finding was made in a cross sectional, not a longitudinal study, our results do not disagree with the previous studies,16 which reported that cognitive symptoms progressed during the course of the disease. In support of our findings, we found that in cases confirmed by necropsy16 (unpublished material), at early disease stages, motor dysfunction was inversely associated with cognitive impairment (unilateral rigidity was inversely correlated with impaired cognition during the first 3 years (r=−0.57, p<0.05); and unilateral dystonia was inversely related to cognitive disturbances at onset (r=−0.63, p<0.01)). Moreover, in the same data set,16 bilateral motor disturbances were positively associated with cognitive disturbances (bilateral bradykinesia was associated with impaired cognition during the first 3 years(r=0.58, p<0.05)). These results suggest that at onset, patients may manifest either motor or cognitive disturbances which reflect the presence of neuronal degeneration in either motor or cognitive circuits. However, when motor symptoms are bilateral, usually with progression of the disease, patients show more obvious cognitive impairment. Because we evaluated patients at relatively early stages of their disease and used the score of the worse limb for the motor assessment, we found that at disease onset, degeneration of the different frontosubcortical circuits does not occur in parallel. It is not surprising that at early stages of the disease, the restricted cognitive disturbances patients exhibited hardly affected their performance on tests which evaluate overall mental status such as the MMSE.
This study has several limitations. It was based on small sample size, thus limiting the generalisation of our findings. In addition, our psychiatric diagnoses were based mainly on a neuropsychiatric rating scale and not on clinical diagnoses. Future studies would benefit from including a larger sample and complete clinical and neuropsychiatric evaluations.
Neuropsychiatric assessment may be helpful to better understand CBD and to better manage patients with this disorder. Future studies need to investigate whether depression in patients with CBD may benefit from treatment with antidepressant agents.
We are grateful to the patients and their relatives for their kind cooperation in our research project and to Mrs Devee Schoenberg for her skillful editorial assistance. This study was supported by an NIA Alzheimer Disease Center grant (AG 10123) and the Sidell-Kogan Foundation. The work was presented in part at the 122nd Annual Meeting of the American Neurological Association, San Diego, California, 28 September to 1 October 1997.