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Published on: August 7, 2017
Functional Connectivity Changes Associated With Depression in Dementia With Lewy Bodies
Manon Querry1, Anne Botzung1,2, Marion Sourty1
1University of Strasbourg and CNRS, ICube Laboratory UMR 7357 and FMTS (Fédération de Médecine Translationnelle de Strasbourg), IMIS Team, Strasbourg, France.
Depressive symptoms in dementia with Lewy bodies (DLB) are linked to altered brain connectivity, particularly between fronto-temporal and visual areas. These changes may impact emotion regulation and cognitive processes in DLB patients.
Area of Science:
- Neuroscience
- Neurology
- Psychiatry
Background:
- Depressive symptoms are common in early dementia with Lewy bodies (DLB), affecting over half of patients.
- Understanding the neural underpinnings of depression in DLB is crucial for early diagnosis and treatment.
Purpose of the Study:
- To investigate functional connectivity (FC) alterations associated with depressive symptoms in prodromal to mild DLB.
- To compare FC in depressed versus non-depressed DLB patients and controls.
Main Methods:
- Utilized MRI data from 66 DLB patients and 18 controls.
- Assessed depression using the Mini International Neuropsychiatric Interview.
- Analyzed resting-state functional connectivity (rsFC) with the CONN toolbox via seed-based approaches.
Main Results:
- Found correlations between depression scores and rsFC between fronto-temporal and visual areas in DLB patients (p < 0.05, FDR corrected).
- Depressed DLB patients exhibited decreased rsFC within the salience network (SN) and between the cerebellar (CN) and fronto-parietal networks (FPN).
- Increased rsFC was observed between the default mode network (DMN) and language network (LN) in depressed DLB patients.
Conclusions:
- Depressive symptoms in DLB are associated with specific rsFC changes, particularly involving fronto-temporal and visual regions.
- These connectivity alterations may contribute to emotional dysregulation, negative bias, and rumination in DLB.
- Antidepressant treatment showed associations with altered FC within key brain networks.
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