TY - JOUR
T1 - Affective bias predicts changes in depression during deep brain stimulation therapy
AU - Cui, Brian
AU - Mocchi, Madaline M.
AU - Metzger, Brian A.
AU - Kalva, Prathik
AU - Magnotti, John F.
AU - Fiedorowicz, Jess G.
AU - Waters, Allison
AU - Kovach, Christopher K.
AU - Reed, Yvonne Y.
AU - Mathura, Raissa K.
AU - Steger, Camille
AU - Pascuzzi, Bailey
AU - Kanja, Kourtney
AU - Veerakumar, Ashan
AU - Tiruvadi, Vineet
AU - Crowell, Andrea
AU - Denison, Lydia
AU - Rozell, Christopher J.
AU - Pouratian, Nader
AU - Goodman, Wayne
AU - Riva Posse, Patricio
AU - Mayberg, Helen S.
AU - Bijanki, Kelly Rowe
N1 - Publisher Copyright:
Copyright © 2025 Cui, Mocchi, Metzger, Kalva, Magnotti, Fiedorowicz, Waters, Kovach, Reed, Mathura, Steger, Pascuzzi, Kanja, Veerakumar, Tiruvadi, Crowell, Denison, Rozell, Pouratian, Goodman, Riva Posse, Mayberg and Bijanki.
PY - 2025
Y1 - 2025
N2 - Introduction: Deep brain stimulation (DBS) is a promising treatment for refractory depression, utilizing surgically implanted electrodes to stimulate specific anatomical targets within the brain. However, limitations of patient-reported and clinician-administered mood assessments pose obstacles in evaluating DBS treatment efficacy. In this study, we investigated whether an affective bias task, which leverages the inherent negative interpretation bias seen in individuals with depression, could serve as a reliable measure of mood changes during DBS therapy in patients with treatment-resistant depression. Methods: Two cohorts of patients (n = 8, n = 2) undergoing DBS for treatment-resistant depression at different academic medical centers completed an affective bias task at multiple time points before and after DBS implantation. The affective bias task involved rating the emotional content of a series of static photographic stimuli of facial expressions throughout their DBS treatment. Patients' ratings were compared with those of non-depressed controls to calculate affective bias scores. Linear mixed-effects modeling was used to assess changes in bias scores over time and their relationship with depression severity measured by the Hamilton Depression Rating Scale (HDRS-17). Results: We observed significant improvements in total affective bias scores over the course of DBS treatment in both cohorts. Pre-DBS, patients exhibited a negative affective bias, which was nearly eliminated post-DBS, with total bias scores approaching those of non-depressed controls. Positive valence trials showed significant improvement post-DBS, while negative valence trials showed no notable change. A control analysis indicated that stimulation status did not significantly affect bias scores, and thus stimulation status was excluded from further modeling. Linear mixed-effects modeling revealed that more negative bias scores were associated with higher HDRS-17 scores, particularly for positive valence stimuli. Additionally, greater time elapsed since DBS implantation was associated with a decrease in HDRS-17 scores, indicating clinical improvement over time. Discussion: Our findings demonstrate that the affective bias task leverages the inherent negative interpretation bias seen in individuals with depression, providing a standardized measure of how these biases change over time. Unlike traditional mood assessments, which rely on subjective introspection, the affective bias task consistently measures changes in mood, offering potential as a tool to monitor mood changes and evaluate the candidacy of DBS treatment in refractory depression.
AB - Introduction: Deep brain stimulation (DBS) is a promising treatment for refractory depression, utilizing surgically implanted electrodes to stimulate specific anatomical targets within the brain. However, limitations of patient-reported and clinician-administered mood assessments pose obstacles in evaluating DBS treatment efficacy. In this study, we investigated whether an affective bias task, which leverages the inherent negative interpretation bias seen in individuals with depression, could serve as a reliable measure of mood changes during DBS therapy in patients with treatment-resistant depression. Methods: Two cohorts of patients (n = 8, n = 2) undergoing DBS for treatment-resistant depression at different academic medical centers completed an affective bias task at multiple time points before and after DBS implantation. The affective bias task involved rating the emotional content of a series of static photographic stimuli of facial expressions throughout their DBS treatment. Patients' ratings were compared with those of non-depressed controls to calculate affective bias scores. Linear mixed-effects modeling was used to assess changes in bias scores over time and their relationship with depression severity measured by the Hamilton Depression Rating Scale (HDRS-17). Results: We observed significant improvements in total affective bias scores over the course of DBS treatment in both cohorts. Pre-DBS, patients exhibited a negative affective bias, which was nearly eliminated post-DBS, with total bias scores approaching those of non-depressed controls. Positive valence trials showed significant improvement post-DBS, while negative valence trials showed no notable change. A control analysis indicated that stimulation status did not significantly affect bias scores, and thus stimulation status was excluded from further modeling. Linear mixed-effects modeling revealed that more negative bias scores were associated with higher HDRS-17 scores, particularly for positive valence stimuli. Additionally, greater time elapsed since DBS implantation was associated with a decrease in HDRS-17 scores, indicating clinical improvement over time. Discussion: Our findings demonstrate that the affective bias task leverages the inherent negative interpretation bias seen in individuals with depression, providing a standardized measure of how these biases change over time. Unlike traditional mood assessments, which rely on subjective introspection, the affective bias task consistently measures changes in mood, offering potential as a tool to monitor mood changes and evaluate the candidacy of DBS treatment in refractory depression.
KW - affective bias
KW - deep brain stimulation
KW - facial emotion
KW - mood proxy
KW - subcallosal cingulate
KW - treatment-resistant depression
KW - ventral capsule striatum
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U2 - 10.3389/fnhum.2025.1539857
DO - 10.3389/fnhum.2025.1539857
M3 - Article
C2 - 40201337
AN - SCOPUS:105002160588
SN - 1662-5161
VL - 19
JO - Frontiers in Human Neuroscience
JF - Frontiers in Human Neuroscience
M1 - 1539857
ER -