Journal
CNS SPECTRUMS
Volume 13, Issue 9, Pages 805-814Publisher
CAMBRIDGE UNIV PRESS
DOI: 10.1017/S1092852900013936
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Funding
- Stockholm County Council
- Swedish Psychiatric Association
- Svenska Lundbeckstiftelsen
- Swedish Medical Research Council
- CNR
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Introduction: Tc-99m-d, l-hexamethylpropylene amine oxime (Tc-99m-HMPAO) retention in brain is proportional to cerebral blood flow and related to both the local hemodynamic state and to the cellular content of reduced glutathione. Alterations of the regional distribution of Tc-99m-HMPAO retention, with discrepant results, have been reported at functional brain imaging of unipolar depression. Since mitochondrial involvement has been reported in depressed patients, the aim of the study was to explore whether the Tc-99m-HMPAO retention at single-photon emission computed tomography in depressed patients may relate to different levels of mitochondrial function. Methods: All patients had audiological and muscular symptoms, somatic symptoms that are common in depression. Citrate synthase (CS) activity assessed in muscle mitochondria correlated strongly with the activities of three mitochondrial respiratory chain enzymes and was used as a marker of mitochondrial function. K-means clustering performed on CS grouped eight patients with low and 11 patients with normal CS. Voxel-based analysis was performed on the two groups by statistical parametric mapping. Results: Voxel-based analysis showed significantly higher Tc-99m-HMPAO retention in the patients with low CS compared with the patients with normal CS in the posterior and inferior frontal cortex, the superior and posterior temporal cortex, the somato-sensory cortex, and the associative parietal cortex. Conclusion: Low muscle CS in depressed patients is related to higher regional Tc-99m-HMPAO retention that may reflect cerebrovascular adaptation to impaired intracellular metabolism and/or intracellular enzymatic changes, as previously reported in mitochondrial disorder. Mitochondrial dysfunction in varying proportions of the subjects may explain some of the discrepant results for Tc-99m-HMPAO retention in depression.
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