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AS06-03 - Lithium: Neuroimaging Evidence of Neuroprotection and its Implication for Bipolar Disorder

Published online by Cambridge University Press:  15 April 2020

T. Hajek
Affiliation:
Dalhousie University, Halifax, NS, Canada Charles University in Prague, Third Faculty of Medicine, Prague, Czech Republic
J. Cullis
Affiliation:
Dalhousie University, Halifax, NS, Canada
R. Blagdon
Affiliation:
Dalhousie University, Halifax, NS, Canada
C. O’Donovan
Affiliation:
Dalhousie University, Halifax, NS, Canada
M. Bauer
Affiliation:
University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
A. Pfennig
Affiliation:
University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
T. Young
Affiliation:
University of Toronto, Toronto, ON
G. MacQueen
Affiliation:
University of Calgary, Calgary, AB, Canada
M. Alda
Affiliation:
Dalhousie University, Halifax, NS, Canada

Abstract

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Introduction

Neuroprotective effects of lithium have been well documented in tissue cultures and animal models. The evidence for lithium related neuroprotection in human subjects is limited and inconsistent, likely due to methodological heterogeneity.

Aims

To investigate the effects of lithium on brain chemistry and structure, we recruited bipolar patients selected for substantial illness burden and varied the exposure to lithium by using strict inclusion criteria.

Methods

We obtained 1.5T magnetic resonance imaging data from 27 bipolar patients with at least 2 years of ongoing lithium treatment (Li group), 16 subjects with < 3 months lifetime exposure to lithium >2 years ago (non-Li group) and 21 healthy controls. Patient groups had to have at least 10 years of illness and 5 episodes.

Results

The non-Li group had significantly lower hippocampal volumes (t = 4.68,corrected p < 0.05) and prefrontal cortex N-acetyl aspartate (NAA) levels (t = −2.91,corrected p < 0.05) than controls, who showed comparable hippocampal volumes and NAA levels to the Li treated subjects. Duration of illness was negatively associated with NAA levels only in the non-Li, but not the Li group.

Conclusions

Among patients selected for substantial illness burden, only those with no or minimal lifetime Li exposure had significantly lower prefrontal NAA levels and hippocampal volumes than controls. Patients with at least 2 years of ongoing Li treatment showed no such changes, despite substantial burden of illness. These findings provide indirect support for neuroprotective effects of lithium and negative effects of illness burden on brain chemistry and structure in patients with bipolar disorders.

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Abstract
Copyright
Copyright © European Psychiatric Association 2012
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