TY - JOUR
T1 - Deep brain stimulation modulates directional limbic connectivity in major depressive disorder
AU - Fridgeirsson, Egill A.
AU - Bergfeld, Isidoor
AU - de Kwaasteniet, Bart P.
AU - Luigjes, Judy
AU - van Laarhoven, Jan
AU - Notten, Peter
AU - Beute, Guus
AU - van den Munckhof, Pepijn
AU - Schuurman, Rick
AU - Denys, Damiaan
AU - van Wingen, Guido
N1 - Publisher Copyright:
© The Author(s), 2025. Published by Cambridge University Press.
PY - 2025/8/8
Y1 - 2025/8/8
N2 - Background Deep brain stimulation (DBS) is being investigated as a treatment for patients with refractory major depressive disorder (MDD). However, little is known about how DBS exerts its antidepressive effects. Here, we investigated whether ventral anterior limb of the internal capsule stimulation modulates a limbic network centered around the amygdala in patients with treatment-resistant MDD. Methods Nine patients underwent resting state functional magnetic resonance scans before DBS surgery and after 1 year of treatment. In addition, they were scanned twice within 2 weeks during the subsequent double-blind cross-over phase with active and sham treatment. Twelve matched controls underwent scans at the same time intervals to account for test-retest effects. The imaging data were investigated with functional connectivity (FC) analysis and dynamic causal modelling. Results Results showed that 1 year of DBS treatment was associated with increased FC of the left amygdala with precentral cortex and left insula, along with decreased bilateral connectivity between nucleus accumbens and ventromedial prefrontal cortex. No changes in FC were observed during the cross-over phase. Effective connectivity analyses using dynamic causal models revealed widespread amygdala-centric changes between presurgery and 1 year follow-up, while the cross-over phase was associated with insula-centric changes between active and sham stimulation. Conclusions These results suggest that ventral anterior limb of the internal capsule DBS results in complex rebalancing of the limbic network involved in emotion, reward, and interoceptive processing.
AB - Background Deep brain stimulation (DBS) is being investigated as a treatment for patients with refractory major depressive disorder (MDD). However, little is known about how DBS exerts its antidepressive effects. Here, we investigated whether ventral anterior limb of the internal capsule stimulation modulates a limbic network centered around the amygdala in patients with treatment-resistant MDD. Methods Nine patients underwent resting state functional magnetic resonance scans before DBS surgery and after 1 year of treatment. In addition, they were scanned twice within 2 weeks during the subsequent double-blind cross-over phase with active and sham treatment. Twelve matched controls underwent scans at the same time intervals to account for test-retest effects. The imaging data were investigated with functional connectivity (FC) analysis and dynamic causal modelling. Results Results showed that 1 year of DBS treatment was associated with increased FC of the left amygdala with precentral cortex and left insula, along with decreased bilateral connectivity between nucleus accumbens and ventromedial prefrontal cortex. No changes in FC were observed during the cross-over phase. Effective connectivity analyses using dynamic causal models revealed widespread amygdala-centric changes between presurgery and 1 year follow-up, while the cross-over phase was associated with insula-centric changes between active and sham stimulation. Conclusions These results suggest that ventral anterior limb of the internal capsule DBS results in complex rebalancing of the limbic network involved in emotion, reward, and interoceptive processing.
KW - deep brain stimulation
KW - dynamic causal models
KW - effective connectivity
KW - limbic network
KW - major depressive disorder
KW - resting state functional connectivity
UR - https://www.scopus.com/pages/publications/105012872333
U2 - 10.1017/S0033291725100767
DO - 10.1017/S0033291725100767
M3 - Article
C2 - 40776411
AN - SCOPUS:105012872333
SN - 0033-2917
VL - 55
JO - Psychological medicine
JF - Psychological medicine
M1 - e231
ER -