Brief Report
Apathy Is Not Associated with Basal Ganglia Atrophy in Frontotemporal Dementia

https://doi.org/10.1097/JGP.0b013e3181b047ffGet rights and content

Objective:

To determine whether basal ganglia atrophy, known to be associated with apathy in nondementia populations, was associated with presence of apathy in patients with frontotemporal dementia (FTD).

Methods:

A cross-sectional case study was conducted at two tertiary dementia care clinics in Toronto, Ontario, Canada. Striatal and thalamic gray matter volumes and apathy measures were collected from 21 subjects with FTD, 6 of whom did not show apathy on the Neuropsychiatric Inventory.

Results:

No significant differences in gray matter volumes were found between apathetic and nonapathetic groups for the striatum or the thalamus.

Conclusions:

Our findings imply that the etiology of apathy seen in patients with FTD differs from that of patients with apathy after acquired injuries to the basal ganglia. Further study is needed to determine whether posterior thalamic atrophy correlates with apathy in FTD or functional imaging techniques might successfully find a relationship between basal ganglia dysfunction and apathy.

Section snippets

METHODS

This study and methods of obtaining consent were approved by Research Ethics Boards at Sunnybrook Health Sciences Centre and Baycrest. In a previous study, we assessed a sample of 21 subjects with FTD and 21 age- and gender-matched healthy comparison subjects for striatal and thalamic atrophy and found that subjects with FTD, especially those more impaired in activities of daily living, had atrophy in the left anterior thalamus and bilaterally in the striatum.4

Our sample consisted of 21

RESULTS

Of the 21 subjects with FTD, 15 had apathy and 6 did not. Given the findings reported by Levy and Dubois, we suspected that the apathetic subjects with FTD would have significantly more atrophy (smaller mean VOI) than those who did not demonstrate apathy by independent samples t-test.

There were no significant differences between VOI direct measures from apathetic versus nonapathetic groups. Although both posterior thalamic mean VOIs of apathetic subjects were smaller than those in the

CONCLUSIONS

We did not find differences in subcortical atrophy for subjects with FTD with or without apathy. The lack of positive finding may be related to small sample size (N = 21) and a resulting lack of power to detect a difference with small effect size.

These results may suggest that the apathy exhibited in patients with FTD differs in etiology from that of patients with apathy due to the acquired, nonneurodegenerative BG lesions, as reported by Levy and Dubois. The damage assessed in these articles

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