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Hippocampal volumes in bipolar disorders: opposing effects of illness burden and lithium treatment
Tomas Hajek1, Jeffrey Cullis, Tomas Novak
1Department of Psychiatry, Dalhousie University, Halifax, NS, Canada. tomas.hajek@dal.ca
Insights
Lithium treatment may protect against hippocampal volume loss in bipolar disorder (BD). Patients with long-term lithium exposure or young patients showed normal hippocampal volumes, unlike those with limited lithium use.
Area of Science:
- Neuroscience
- Psychiatry
- Radiology
Background:
- Hippocampal volume reduction is common in unipolar depression.
- Bipolar disorder (BD) studies often show no hippocampal volume changes, possibly due to lithium's (Li) neuroprotective effects.
Purpose of the Study:
- To investigate the neuroprotective effects of lithium (Li) on hippocampal volume in bipolar disorder (BD).
- To compare hippocampal volumes in BD patients with varying lithium exposure histories and healthy controls.
Main Methods:
- Compared hippocampal volumes using MRI in three groups: BD patients with long-term Li treatment (Li group), BD patients with minimal Li exposure (non-Li group), and healthy controls.
- Also compared young, Li-naïve BD patients with age-matched controls.
Main Results:
- The non-Li group showed significantly smaller left hippocampal volumes than controls.
- The Li group and young Li-naïve BD patients had hippocampal volumes comparable to controls.
- A trend suggested lower hippocampal volumes in the non-Li group compared to the Li group.
Conclusions:
- Long-term lithium treatment or being young and Li-naïve may preserve hippocampal volume in bipolar disorder.
- Illness burden appears to negatively impact hippocampal volumes in BD, while lithium may offer neuroprotection.
Objective:
Hippocampal volume decrease associated with illness burden is among the most replicated findings in unipolar depression. The absence of hippocampal volume changes in most studies of individuals with bipolar disorder (BD) may reflect neuroprotective effects of lithium (Li).
Methods:
We recruited 17 BD patients from specialized Li clinics, with at least two years of regularly monitored Li treatment (Li group), and compared them to 12 BD participants with < 3 months of lifetime Li exposure and no Li treatment within two years prior to the scanning (non-Li group) and 11 healthy controls. All BD patients had at least 10 years of illness and five episodes. We also recruited 13 Li-naïve, young BD participants (15-30 years of age) and 18 sex- and age-matched healthy controls. We compared hippocampal volumes obtained from 1.5-T magnetic resonance imaging (MRI) scans using optimized voxel-based morphometry with small volume correction.
Results:
The non-Li group had smaller left hippocampal volumes than controls (corrected p < 0.05), with a trend for lower volumes than the Li group (corrected p < 0.1), which did not differ from controls. Young, Li-naïve BD patients close to the typical age of onset had comparable hippocampal volumes to controls.
Conclusions:
Whereas patients with limited lifetime Li exposure had significantly lower hippocampal volumes than controls, patients with comparable illness burden, but with over two years of Li treatment, or young Li-naïve BD patients, showed hippocampal volumes comparable to controls. These results provide indirect support for neuroprotective effects of Li and negative effects of illness burden on hippocampal volumes in bipolar disorders.
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