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PAPER |
1 School of Psychiatry and Clinical Neurosciences, University of Western Australia, and Fremantle Hospital, Western Australia, Australia
2 Department of Psychiatry, University of Iowa, Iowa City, USA
3 PET Center for Addiction and Mental Health, Clarke Division, Toronto, Canada
Correspondence to:
Correspondence to:
Professor S E Starkstein
Education Building T-7, Fremantle Hospital, Fremantle, 6959 WA, Australia; ses{at}cyllene.uwa.edu.au
Received 11 April 2005
In final revised form 15 June 2005
Accepted for publication 4 July 2005
 | ABSTRACT |
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 TOP ABSTRACT METHODSRESULTSDISCUSSIONREFERENCES |
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Objectives: To examine the clinical correlates of apathy in Alzheimer’s disease (AD), and to determine whether apathy is a significant predictor of more rapid cognitive, functional and emotional decline.
Methods: Using a structured psychiatric evaluation, we examined a consecutive series of 354 subjects meeting clinical criteria for AD. Apathy was assessed by the Apathy Scale, and diagnosed using standardised criteria. Additional measurements included scales for depression, functional impairment, and global cognitive functions. A follow up evaluation was carried out in 247 patients (70% of the total sample) between 1 and 4 years after the baseline evaluation.
Results: Apathy was significantly associated with older age (p = 0.009), and a higher frequency of minor and major depression (p<0.0001). Apathy at baseline was a significant predictor of depression at follow up (p = 0.01), and was associated with a faster cognitive (p = 0.0007) and functional decline (p = 0.006).
Conclusions: Apathy in AD is a behavioural marker of a more aggressive dementia, characterised by a faster progression of cognitive, functional, and emotional impairment.
Abbreviations: AD, Alzheimer’s disease; ADL, activities of daily living; AS, Apathy Scale; CDR, Clinical Dementia Rating; DSM-IV, Diagnostic and statistical manual of mental disorders, 4th edition; FIM, Functioning Independence Measure; HAM-D, Hamilton depression scale; HIS, Hachinski Ischemic Score; MMSE, Mini Mental State Examination; SCID, Structured Clinical Interview for DSM-IV
Keywords: Alzheimer’s disease; anosognosia; apathy; dementia; depression
Apathy is defined as lack of motivation relative to the individual’s previous level of functioning, and is manifested by diminished goal directed cognition and behaviour.1 Among patients with Alzheimer’s disease (AD) the frequency of apathy has been reported to range from 25% to 50%.2 Depression is the main psychiatric correlate of apathy in AD,3 an expected finding given that loss of interest and motivation is a conspicuous symptom of both syndromes. However, apathy should not be construed as a mere symptom of depression, given that about half of AD patients with apathy have no concomitant depression.3 Apathy is most prevalent in severe dementia,2 and could result from the serious functional restrictions imposed by the cognitive deficits. Several studies have demonstrated a significant association between apathy and both reduced metabolic activity in prefrontal regions4–6 and more severe parkinsonism,3 suggesting that neuropathological changes in specific brain areas may underlie the high frequency of apathy in AD.
For the present study, we examined a large consecutive series of patients with AD using reliable instruments to measure the severity of apathy, to rate the presence and severity of depression, and to determine the stages of AD. We expected apathy at baseline to be significantly associated with more severe dementia and depression, and to predict a faster cognitive and functional decline.
| METHODS |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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Psychiatric examination
After written informed consent was obtained from patients and their respective caregivers, a psychiatrist blind to neurological findings assessed patients with the following instruments:
Follow up examination
A follow up evaluation was carried out on 247 of the 354 patients (70%) between 1 and 4 years after the initial evaluation, using the same instruments assessed at baseline. Some patients could not be followed up; reasons included death during the follow up period (n = 21; 20%), severe dementia that precluded assessment (n = 49; 46%), moved to another city or could not be traced (n = 23; 21%), or refused another evaluation (n = 14; 13%). Patients without follow up were significantly older than patients with follow up (mean (SD) age: 73.1 (8.1) v 70.7 (7.4); t = 2.9, df = 352, p = 0.003), had lower MMSE scores (mean (SD) scores: 15.2 (7.1) v 22.2 (5.6); t = 9.9, df = 352, p<0.0001), and more severe apathy (mean (SD) scores: 22.7 (9.3) v 18.1 (9.6); t = 4.4, df = 352, p<0.0001). In total, 207 (84%) of the 247 patients with a follow up were assessed 1–2 years after the baseline evaluation, 30 patients (12%) had a follow up evaluation 2–3 years after the baseline evaluation, and 10 patients (4%) had a follow up evaluation 3–4 years after the baseline evaluation.
Statistical analysis
Statistical analysis was carried out using means and SDs, Student’s t test, and one way and repeated measures analysis of variance with post hoc planned comparisons (Tukey’s test for unequal samples). Frequency distributions were calculated using 
2 and Fisher’s exact tests. All p values are two tailed. To reduce the risk of type I errors, the p value was set at 0.01.
| RESULTS |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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). The frequency of apathy was 14% (n = 8) in very mild AD (CDR 0.5), 28% (n = 39) in mild AD (CDR 1), 39% (n = 43) in moderate AD (CDR 2), and 61% (n = 30) in severe AD (CDR 3). A hypothesis of unequal frequency of apathy based on the stage of dementia was statistically substantiated (2 = 29.9, df = 3, p<0.0001). Of the 74 patients with major depression, 41 (55%) had apathy, compared with 35 of 85 (41%) patients with minor depression, and 45 of 195 (23%) patients without depression. A hypothesis of unequal frequency of apathy based on the presence of depression was statistically substantiated (2 = 26.8, df = 2, p<0.0001).
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). These results demonstrate an overall significant increment in apathy scores during the follow up period, and overall higher apathy scores for the group with major depression at follow up. The lack of a significant group by time interaction indicates that the increment in apathy scores during the follow up period was of similar magnitude for all three groups.
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Apathy and functional decline
To determine whether apathy predicted a faster cognitive and functional decline we examined longitudinal differences on MMSE and FIM scores for the following groups: (a) apathy at baseline and follow up,(b) no apathy at baseline or at follow up, and (c) no apathy at baseline and apathy at follow up (the small sample of 8 patients with apathy at baseline but no apathy at follow up was not included in this analysis) (table 3). Repeated measures analysis of variance for MMSE scores, with baseline MMSE scores as the covariate, showed a significant group effect (F(2,236) = 8.70, p = 0.0002), the expected time effect (F(1,236) = 33.8, p<0.0001), and a significant group by time interaction (F(2,236) = 7.39, p = 0.0007) (table 3). On individual group comparisons, patients with no apathy at baseline but apathy at follow up had a significantly greater decline on MMSE scores than patients without apathy at both evaluations (F(1,177) = 15.7, p<0.0001).
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). On individual group comparisons, patients with no apathy at baseline but apathy at follow up had a significantly greater functional decline than patients without apathy at both evaluations (F(1,163) = 11.2, p<0.001). There were no significant between group differences at the follow up evaluation in the frequency of patients on anticholinesterase drugs (no apathy at both evaluations: 36%, no apathy at baseline, apathy at follow up: 47%, apathy at both evaluations: 37%), neuroleptics (15%, 25%, and 25%, respectively), anxiolytics (23%, 24%, and 21%, respectively), and antidepressants (19%, 26%, and 30%, respectively).
| DISCUSSION |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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Before further comments, several limitations of our study should be pointed out. Firstly, we obtained longitudinal information on 70% of our sample. The main reasons for lack of follow up were death or extreme dementia, and change of address. Patients without a follow up evaluation were older and had more severe dementia and apathy than patients with a follow up, thus our findings should be restricted to patients with mild or moderate AD. Secondly, duration of follow up was not homogeneous, ranging from 1 to 4 years. However, 84% of the patients were assessed 1–2 years after the baseline evaluation, and duration of follow up was similar for all the subgroups that were analysed. Thirdly, apathy in AD may be better suited to dimensional rather than a categorical diagnosis, and this issue should be clarified in future studies. However, we have demonstrated the reliability and validity of a categorical diagnosis of apathy in AD.3,17 Finally, patients were recruited from a tertiary neurology centre, which may have biased our sample towards cases with relatively more severe psychopathology.
To our knowledge, this is the largest longitudinal study on the clinical correlates and prognostic implications of apathy in AD. We found that patients with apathy were significantly older than patients without, and the frequency of apathy was highest among patients with severe dementia. Patients with advanced AD are greatly limited in the range of goal directed activities, and older age is itself associated with decreased social interaction. On the other hand, our finding that apathy was relatively frequent in the stages of mild (28%) and moderate AD (39%), and that 39% of patients with severe AD had no apathy suggests that severe cognitive deficits are neither necessary nor sufficient to produce apathy.
Our study also demonstrated a significant association between apathy and depression, an expected finding given phenomenological commonalities between both syndromes. However, depression was neither necessary (23% of non-depressed patients had apathy) nor sufficient (45% of patients with major depression and 49% of patients with minor depression had no apathy) to produce apathy. These findings support the suggestion from Levy that apathy should not be construed as a mere symptom of depression in dementia.18 Moreover, our study demonstrated that patients who became depressed during the follow up period did not develop more severe apathy at follow up than patients without depression, supporting the nosological separation between apathy and depression in AD.
In a recent study, Boyle and coworkers19 found that after accounting for both depression and cognitive deficits, apathy was significantly correlated with more severe functional deficits. Our study not only replicated this association, but also demonstrated for the first time that patients who developed apathy during the follow up period had a more rapid cognitive and functional decline than patients without apathy. These findings suggest that apathy is a behavioural marker of a more "malignant" type of AD, with more severe behavioural problems and a faster progression of cognitive, functional, and emotional deficits. Whether the successful treatment of apathy may reduce the progression of these impairments and improve the quality of life for patients and caregivers should be examined in future studies.
| ACKNOWLEDGEMENTS |
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| FOOTNOTES |
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| REFERENCES |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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