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Published on: April 26, 2024
Night sleep influences white matter microstructure in bipolar depression
Francesco Benedetti1, Elisa M T Melloni1, Sara Dallaspezia1
1Department of Clinical Neurosciences and CERMAC, Scientific Institute Ospedale San Raffaele and Vita-Salute San Raffaele University, Milano, Italy.
Bipolar disorder (BD) patients show altered brain white matter (WM) microstructure linked to sleep disruption. Diffusion tensor imaging (DTI) revealed associations between WM integrity and sleep quantity, suggesting a connection between sleep and brain structure in BD.
Area of Science:
- Neuroimaging
- Sleep Medicine
- Psychiatry
Background:
- Circadian rhythm alterations and sleep disruption are key features of bipolar disorder (BD).
- Diffusion tensor imaging (DTI) indicates widespread white matter (WM) microstructure changes in BD patients.
- Sleep is crucial for myelination and oligodendrocyte precursor cell proliferation.
Purpose of the Study:
- To investigate the association between DTI-derived WM microstructure measures and sleep quantity in individuals with BD.
- To explore how sleep impacts the physical structure of white matter in the brain.
Main Methods:
- Sixty-nine inpatients with a bipolar I disorder depressive episode were studied.
- Whole-brain tract-based spatial statistics analyzed DTI measures (AD, RD, MD, FA) of WM microstructure.
- Sleep quantity was assessed using the Pittsburgh Sleep Quality Index (PSQI) and actigraphy in a subsample.
Main Results:
- Fractional anisotropy (FA) positively correlated with actigraphy and PSQI measures of time asleep (TA) and total sleep time (TST).
- Radial diffusivity (RD) showed an inverse association with actigraphy and PSQI measures of TA and TST.
- Affected WM tracts included the corpus callosum, cingulate gyrus, and corticospinal tract, among others.
Conclusions:
- Findings suggest a link between sleep disruption and altered WM microstructure (reduced FA, increased RD) in specific brain tracts in BD.
- These microstructural changes may impact functional connectivity within the brain in individuals with BD.
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