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Lithium alters brain activation in bipolar disorder in a task- and state-dependent manner: an fMRI study

Peter H Silverstone1 email, Emily C Bell1 email, Morgan C Willson2 email, Sanjay Dave1 email and Alan H Wilman2 email

Department of Psychiatry, Faculty of Medicine, University of Alberta, 1E1.07 MacKenzie Center, 8440-112 Street, Edmonton, Alberta, T6G 2B7, Canada

Department of Biomedical Engineering, Faculty of Medicine, University of Alberta, 1071 Research Transition Facility, 8308-114 Street, Edmonton, Alberta, T6G 2V2, Canada

author email corresponding author email

Annals of General Psychiatry 2005, 4:14doi:10.1186/1744-859X-4-14

Published: 19 July 2005

Abstract

Background

It is unknown if medications used to treat bipolar disorder have effects on brain activation, and whether or not any such changes are mood-independent.

Methods

Patients with bipolar disorder who were depressed (n = 5) or euthymic (n = 5) were examined using fMRI before, and 14 days after, being started on lithium (as monotherapy in 6 of these patients). Patients were examined using a word generation task and verbal memory task, both of which have been shown to be sensitive to change in previous fMRI studies. Differences in blood oxygenated level dependent (BOLD) magnitude between the pre- and post-lithium results were determined in previously defined regions of interest. Severity of mood was determined by the Hamilton Depression Scale for Depression (HAM-D) and the Young mania rating scale (YMRS).

Results

The mean HAM-D score at baseline in the depressed group was 15.4 ± 0.7, and after 2 weeks of lithium it was 11.0 ± 2.6. In the euthymic group it was 7.6 ± 1.4 and 3.2 ± 1.3 respectively. At baseline mean BOLD signal magnitude in the regions of interest for the euthymic and depressed patients were similar in both the word generation task (1.56 ± 0.10 and 1.49 ± 0.10 respectively) and working memory task (1.02 ± 0.04 and 1.12 ± 0.06 respectively). However, after lithium the mean BOLD signal decreased significantly in the euthymic group in the word generation task only (1.56 ± 0.10 to 1.00 ± 0.07, p < 0.001). Post-hoc analysis showed that these differences were statistically significant in Broca's area, the left pre-central gyrus, and the supplemental motor area.

Conclusion

This is the first study to examine the effects of lithium on brain activation in bipolar patients. The results suggest that lithium has an effect on euthymic patients very similar to that seen in healthy volunteers. The same effects are not seen in depressed bipolar patients, although it is uncertain if this lack of change is linked to the lack of major improvements in mood in this group of patients. In conclusion, this study suggests that lithium may have effects on brain activation that are task- and state-dependent. Given the small study size and the mildness of the patient's depression these results require replication.


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