Motor Performance and Functional Connectivity Between the Posterior Cingulate Cortex and Supplementary Motor Cortex in Bipolar and Unipolar Depression
Overview
Authors
Affiliations
Although implicated in unsuccessful treatment, psychomotor deficits and their neurobiological underpinnings in bipolar (BD) and unipolar (UD) depression remain poorly investigated. Here, we hypothesized that motor performance deficits in depressed patients would relate to basal functional coupling of the hand primary motor cortex (M1) and the posterior cingulate cortex (PCC) with the supplementary motor area (SMA). We performed a longitudinal, naturalistic study in BD, UD and matched healthy controls comprising of two resting-state functional MRI measurements five weeks apart and accompanying assessments of motor performance using a finger tapping task (FTT). A subject-specific seed-based analysis describing functional connectivity between PCC-SMA as well as M1-SMA was conducted. The basal relationships with motor performance were investigated using linear regression models and all measures were compared across groups. Performance in FTT was impaired in BD in comparison to HC in both sessions. Behavioral performance across groups correlated significantly with resting state functional coupling of PCC-SMA, but not of M1-SMA regions. This relationship was partially reflected in a reduced PCC-SMA connectivity in BD vs HC in the second session. Exploratory evaluation of large-scale networks coupling (SMN-DMN) exhibited no correlation to motor performance. Our results shed new light on the association between the degree of disruption in the SMA-PCC anticorrelation and the level of motor impairment in BD.
Andrade K, Pacella V Commun Biol. 2024; 7(1):1384.
PMID: 39448784 PMC: 11502706. DOI: 10.1038/s42003-024-07076-7.
Zhang J, Li Y, Liu X, Zhong D, Xue C, Fan J Brain Behav. 2024; 14(10):e70071.
PMID: 39378277 PMC: 11460607. DOI: 10.1002/brb3.70071.
From pathogenesis of stress-related mental disorders to treatment: beyond the brain.
Liu X, Lu L Eur Arch Psychiatry Clin Neurosci. 2024; 274(3):473-474.
PMID: 38519738 DOI: 10.1007/s00406-024-01791-2.